Bishwajit Saikia*, Preeti Rekha Boruah, Abdul Aziz Ali and Diganta Sarma. Contents
|
|
- Πράξις Γιάγκος
- 7 χρόνια πριν
- Προβολές:
Transcript
1 Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2015 Supporting Information On-water organic synthesis: A green, highly efficient, low cost and reusable catalyst system for biaryl synthesis under aerobic conditions at room temperature Bishwajit Saikia*, Preeti Rekha Boruah, Abdul Aziz Ali and Diganta Sarma Department of Chemistry, Dibrugarh University, Dibrugarh , Assam, India Tel: ; bishwajitsaikia@gmail.com (B. Saikia) Contents Materials and Methods General experimental procedure P1 P1 Characterization data of the product of the Suzuki reaction P2 P9 References P9 P11 1 H and 13 C NMR spectra for cross-coupling products P12 P41
2 Materials and Methods All aryl/heteroaryl bromides and arylboronic acids were used as received (Alfa Aesar, MARC, Sigma- Aldrich). All other chemicals were purchased from commercial sources and used without further purification. 1 H NMR and 13 C NMR spectra were recorded at 500 MHz using TMS as internal standard. Mass spectroscopy data of the product of Suzuki reaction was collected on a MS-EI instrument. General experimental procedure In a round bottomed flask, a mixture of aryl/heteroaryl halide (1 mmol), arylboronic acid (1.2 mmol), PdCl 2 (0.01 mmol), sucrose (0.005 mmol) and K 2 CO 3 (1.2 mmol) in H 2 O (3 ml) and the mixture was stirred at room temperature for a time period as mentioned in Table 2 in the manuscript. The progress of the reaction was monitored by TLC. After completion of the reaction it was extracted with diethyl ether (3 x 10 ml) and washed with water. The combined ether extract was dried over anhydrous Na 2 SO 4. The filtrate was concentrated under reduced pressure. The product was purified by column chromatography over silica gel using n-hexane/ethyl acetate (9:1 v/v) to get the desired coupling product. The products were characterized by IR, 1 H NMR and 13 C NMR spectroscopy. 1 P a g e
3 Characterization data of the product of the Suzuki reaction 1-22 MeO 4-Methoxybiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ (m, 4 H), 7.42 (t, 2 H, J = 8 Hz), 7.28 (t, 1 H, J = 15 Hz), 6.98 (d, 2 H, J = 5 Hz), 3.85 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): δ 161.5, 139, 129, 128.8, 128.5, 127.6, 127.5, , , , , 114.7, 57.6; MS (EI): m/z (%) = 184 (100) [M+]. MeO 3-Methoxybiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ (m, 2 H), (m, 2 H), (m, 2 H), (m, 1 H), (m, 1 H), 6.90 (ddd, 1 H, J = 10, 7.5, 1.5 Hz), 3.86 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): δ 161.7, 139, 129, 128.8, 128.5, 127.6, 127.5, , , , 127.2, 113, 57; MS (EI): m/z (%) = 184 (100) [M+]. 2 P a g e
4 Me OMe 4-Methoxy-4 / -methylbiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ 7.51 (d, 2 H, J = 8.0 Hz), 7.45 (d, 2 H, J = 8.0 Hz), 7.22 (d, 2 H, J = 8.0 Hz), 6.97 (d, 2 H, J = 8.5 Hz), 3.84 (s, 3 H), 2.38 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): 158.7, 137.8, 136.2, 133.6, 129.3, 127.8, 126.4, 114, 55.2, 20.9; MS (EI): m/z (%) = 198 (100) [M+]. NC Biphenyl-4-carbonitrile 1 H NMR (500 MHz, CDCl 3, TMS): δ 7.73 (d, 2 H, J = 8.4 Hz), 7.69 (d, 2 H, J = 8.5 Hz), 7.58 (t, 2 H, J = 4.5 Hz), 7.48 (t, 2 H, J = 7.5 Hz), (m, 1 H); 13 C NMR (125 MHz, CDCl 3, TMS): 145.5, 139.6, 132.5, 129.0, 128.5, 127.6, 127.5, , , , 127.1, 118.8, 110.7; MS (EI): m/z (%) = 179 (100) [M+]. 3 P a g e
5 OHC Biphenyl-4-carbaldehyde 1 H NMR (500 MHz, CDCl 3, TMS): δ 1.08 (s, 1 H), 7.95 (d, 2 H, J = 1.5 Hz), 7.79 (d, 2 H, J = 1.5 Hz), 7.65 (d, 2 H, J = 1.5 Hz), 7.49 (t, 2 H, J = 1.0 Hz), 7.43 (t, 1 H, J = 1.5 Hz); 13 C NMR (125 MHz, CDCl 3, TMS): 192.2, 145.8, 137.6, 133.5, 130.6, 130.3, 129.9, 128.1, 127.9, 127.8, 127.6, 127.5, 127.4; MS (EI): m/z (%) = 182 (100) [M+]. OHC Biphenyl-3-carbaldehyde 1 H NMR (500 MHz, CDCl 3, TMS): δ 9.85 (s, 1 H), 8.04 (s, 1 H), (m, 2 H), (m, 1 H), 7.48 (d, 2 H, J = 1.0 Hz), (m, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): 192.4, 145.8, 137.6, , , 129.9, 129.8, 129.5, 128.5, 128.3, 127.5, , ; MS (EI): m/z (%) = 182 (100) [M+]. 4 P a g e
6 CHO Biphenyl-2-carbaldehyde 1 H NMR (500 MHz, CDCl 3, TMS): δ 9.9 (s, 1 H), 8.02 (d, 1 H, J = 1 Hz), (m, 2 H), (m, 6 H); 13 C NMR (125 MHz, CDCl 3, TMS): 192.3, 145.8, 137.6, , , 130.2, 129.9, 129.5, 127.9, 127.8, 127.6, 127.5, 127.4; MS (EI): m/z (%) = 182 (100) [M+]. H 3 C O C 1-Biphenyl-4-yl-ethanone 1 H NMR (500 MHz, CDCl 3, TMS): δ 8.04 (d, 2 H, J = 7.0 Hz), 7.69 (d, 2 H, J = 5.0 Hz), 7.63 (t, 2 H, J = 5.5 Hz), 7.49 (t, 2 H, J = 7.5 Hz), (m, 1 H), 2.64 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): 197.7, 145.6, 139.7, 135.7, , , , , , 26.6; MS (EI): m/z (%) = 196 (51) [M+]. 5 P a g e
7 O 2 N 4-Nitrobiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ 8.31 (d, 2 H, J = 7.5 Hz), 7.75 (d, 2 H, J = 9.0 Hz), 7.64 (d, 2 H, J = 7.0 Hz), 7.51 (t, 2 H, J = 7.5 Hz), 7.46 (t, 1 H, J = 7.2 Hz); 13 C NMR (125 MHz, CDCl 3, TMS): 147.6, 142.7, 135.7, , , , , ; MS (EI): m/z (%) = 199 (100) [M+]. MeO CF 3 4-Methoxy-4 / -trifluoromethylbiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ 7.54 (d, 2 H, J = 3.0 Hz), 7.5 (d, 2 H, J = 2.0 Hz), 7.19 (d, 2 H, J = 7.5 Hz), 6.96 (d, 2 H, J = 2 Hz), 3.84 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): 161.3, 139, 129, 128.8, 128.5, 127.6, 127.5, , , , , , , 57.1; MS (EI): m/z (%) = 252 (100) [M+]. 6 P a g e
8 O 2 N CH 3 4 / -Methyl-4-nitrobiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ 8.29 (d, 2 H, J = 2.5 Hz), 7.72 (d, 2 H, J = 4.5 Hz), 7.35 (d, 2 H, J = 8.5 Hz), 7.29 (d, 2 H, J = 11.5 Hz), 2.42 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): 147.4, 146.7, 138.9, 135.7, 129.7, 127.3, 127.1, 123.9, 21.1; MS (EI): m/z (%) = 213 (100) [M+]. MeO H 3 C 4 / -Methoxy-2-methylbiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ (m, 6 H), 6.90 (d, 2 H, J = 2.0 Hz), 3.8 (s, 3 H), 2.2 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): 158.3, 141.4, 135.3, 134.2, , , 129.7, 126.8, 125.6, 113.3, 55.1, 20.4; MS (EI): m/z (%) = 198 (100) [M+]. 7 P a g e
9 Me CF 3 4 / -Methyl-4-trifluoromethylbiphenyl 1 H NMR (500 MHz, CDCl 3, TMS): δ 7.67 (s, 4 H), 7.50 (d, 2 H, J = 8.1 Hz), 7.29 (d, 2 H, J = 8.0 Hz), 2.41 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): 139, 136.8, 133, 129, 128.8, 128.5, 127.6, 127.5, , , , , 119, 20; MS (EI): m/z (%) = 236 (100) [M+]. S OMe 3-(4-Methoxy-phenyl)-thiophene 1 H NMR (500 MHz, CDCl 3, TMS): δ 7.52 (d, 2 H, J = 1.5 Hz), (m, 3 H), 6.94 (d, 2 H, J = 7.0 Hz), 3.84 (s, 3 H); 13 C NMR (125 MHz, CDCl 3, TMS): δ 158.7, 141.8, 128.6, 127.4, 125.9, 123.7, 114, 55.2; MS (EI): m/z (%) = 190 (100) [M+]. 8 P a g e
10 N 2-Phenylpyridine 1 H NMR (500 MHz, CDCl 3, TMS): δ 8.3 (s, 1 H), (m, 2 H), (m, 2 H), (m, 3 H), (m, 1 H); 13 C NMR (125 MHz, CDCl 3, TMS): δ 157.3, 149.5, 139.2, 136.6, 128.7, 128.5, 126.8, 121.9, 120.4; MS (EI) m/z 155 (M+, 100%); MS (EI): m/z (%) = 155 (100) [M+]. References 1. L. Liu, Y. Zhang and Y. Wang, J. Org. Chem., 2005, 70, L. Liu, Y. Zhang and B. Xin, J. Org. Chem., 2006, 71, Y. M. A. Yamada, K. Takeda, H. Takahashi and S. Ikegami, J. Org. Chem., 2003, 68, O. Navarro, H. Kaur, P. Mahjoor and S. P. Nolan, J. Org. Chem., 2004, 69, X.-H. Fan and L.-M. Yang, Eur. J. Org. Chem., 2011, P a g e
11 6. Y. Kitamura, S. Sako, T. Udzu, A. Tsutsui, T. Maegawa, Y. Monguchi and H. Sajiki, Chem. Commun., 2007, R. Zhong, A. Pothig, Y. Feng, K. Riener, W. A. Herrmann and F. E. Kuhn, Green Chem., 2014, 16, J. Han, Y. Liu and R. Guo, J. Am. Chem. Soc., 2009, 131, C. Baillie, L. Zhang and J. Xiao, J. Org. Chem., 2004, 69, J. V. Kingston and J. G. Verkade, J. Org. Chem., 2007, 72, S. C. Sau, S. Santra, T. K. Sen, S. K. Mandal and D. Koley, Chem. Commun., 2012, 48, S. Li, Y. Lin, J. Cao and S. Zhang, J. Org. Chem., 2007, 72, T. Fujihara, S. Yoshida, J. Terao and Y. Tsuji, Org. Lett., 2009, 11, C. Song, Y. Ma, Q. Chai, C. Ma, W. Jiang and M. B. Andrus, Tetrahedron, 2005, 61, D.-H. Lee and M.-J. Jin, Org. Lett., 2011, 13, C. M. So, C. C. Yeung, C. P. Lau and F. Y. Kwong, J. Org. Chem., 2008, 73, H. Yang, Y. Wang, Y. Qin, Y. Chong, Q. Yang, G. Li, L. Zhang and W. Li, Green Chem., 2011, 13, G. A. Molander, S. L. J. Trice and S. M. Kennedy, J. Org. Chem., 2012, 77, P a g e
12 19. T. Hoshi, T. Honma, A. Mori, M. Konishi, T. Sato, H. Hagiwara and T. Suzuki, J. Org. Chem., 2013, 78, Z. Guan, J. Hu, Y. Gu, H. Zhang, G. Lia and T. Li, Green Chem., 2012, 14, V. Kairouz and A. R. Schmitzer, Green Chem., 2014, 16, J.-P. Wan, C. Wang, R. Zhou and Y. Liu, RSC Adv., 2012, 2, P a g e
13 1 H NMR spectra of MeO 12 P a g e
14 13 C NMR spectra of MeO 13 P a g e
15 1 H NMR spectra of MeO 14 P a g e
16 13 C NMR spectra of MeO 15 P a g e
17 1 H NMR spectra of Me OMe 16 P a g e
18 13 C NMR spectra of Me OMe 17 P a g e
19 1 H NMR spectra of NC 18 P a g e
20 13 C NMR spectra of NC 19 P a g e
21 1 H NMR spectra of OHC 20 P a g e
22 13 C NMR spectra of OHC 21 P a g e
23 1 H NMR spectra of OHC 22 P a g e
24 13 C NMR spectra of OHC 23 P a g e
25 1 H NMR spectra of CHO 24 P a g e
26 13 C NMR spectra of CHO 25 P a g e
27 1 H NMR spectra of H 3 C O C 26 P a g e
28 13 C NMR spectra of H 3 C O C 27 P a g e
29 1 H NMR spectra of O 2 N 28 P a g e
30 13 C NMR spectra of O 2 N 29 P a g e
31 1 H NMR spectra of MeO CF 3 30 P a g e
32 13 C NMR spectra of MeO CF 3 31 P a g e
33 1 H NMR spectra of O 2 N CH 3 32 P a g e
34 13 C NMR spectra of O 2 N CH 3 33 P a g e
35 1 H NMR spectra of MeO H 3 C 34 P a g e
36 13 C NMR spectra of MeO H 3 C 35 P a g e
37 1 H NMR spectra of Me CF 3 36 P a g e
38 13 C NMR spectra of Me CF 3 37 P a g e
39 1 H NMR spectra of S OMe 38 P a g e
40 13 C NMR spectra of S OMe 39 P a g e
41 1 H NMR spectra of N 40 P a g e
42 13 C NMR spectra of N 41 P a g e
ESI for. A simple and efficient protocol for the palladium-catalyzed. ligand-free Suzuki reaction at room temperature in aqueous DMF.
ESI for A simple and efficient protocol for the palladium-catalyzed ligand-free Suzuki reaction at room temperature in aqueous DMF Chun Liu,* Qijian i, Fanying Bao and Jieshan Qiu State Key Laboratory
Διαβάστε περισσότεραCopper-catalyzed formal O-H insertion reaction of α-diazo-1,3-dicarb- onyl compounds to carboxylic acids with the assistance of isocyanide
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2014 Copper-catalyzed formal O-H insertion reaction of α-diazo-1,3-dicarb- onyl compounds to carboxylic
Διαβάστε περισσότεραElectronic Supplementary Information
Electronic Supplementary Information Unprecedented Carbon-Carbon Bond Cleavage in Nucleophilic Aziridine Ring Opening Reaction, Efficient Ring Transformation of Aziridines to Imidazolidin-4-ones Jin-Yuan
Διαβάστε περισσότεραMetal-free Oxidative Coupling of Amines with Sodium Sulfinates: A Mild Access to Sulfonamides
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2014 Supporting information for Metal-free Oxidative Coupling of Amines with Sodium Sulfinates:
Διαβάστε περισσότεραA facile and general route to 3-((trifluoromethyl)thio)benzofurans and 3-((trifluoromethyl)thio)benzothiophenes
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2014 A facile and general route to 3-((trifluoromethyl)thio)benzofurans and 3-((trifluoromethyl)thio)benzothiophenes
Διαβάστε περισσότεραSupporting information
Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2014 Supporting information Copper-catalysed intramolecular O-arylation: a simple
Διαβάστε περισσότεραand Selective Allylic Reduction of Allylic Alcohols and Their Derivatives with Benzyl Alcohol
FeCl 3 6H 2 O-Catalyzed Disproportionation of Allylic Alcohols and Selective Allylic Reduction of Allylic Alcohols and Their Derivatives with Benzyl Alcohol Jialiang Wang, Wen Huang, Zhengxing Zhang, Xu
Διαβάστε περισσότεραSupporting Information
Supporting Information Copper/Silver Cocatalyzed Oxidative Coupling of Vinylarenes with ICH 2 CF 3 or ICH 2 CHF 2 Leading to β-cf 3 /CHF 2 -Substituted Ketones Niannian Yi, Hao Zhang, Chonghui Xu, Wei
Διαβάστε περισσότεραCopper-Catalyzed Oxidative Dehydrogenative N-N Bond. Formation for the Synthesis of N,N -Diarylindazol-3-ones
Electronic Supplementary Material (ESI) for Organic Chemistry Frontiers. This journal is the Partner Organisations 2016 Supporting information Copper-Catalyzed Oxidative Dehydrogenative - Bond Formation
Διαβάστε περισσότεραFree Radical Initiated Coupling Reaction of Alcohols and. Alkynes: not C-O but C-C Bond Formation. Context. General information 2. Typical procedure 2
Free Radical Initiated Coupling Reaction of Alcohols and Alkynes: not C-O but C-C Bond Formation Zhongquan Liu,* Liang Sun, Jianguo Wang, Jie Han, Yankai Zhao, Bo Zhou Institute of Organic Chemistry, Gannan
Διαβάστε περισσότεραIodine-catalyzed synthesis of sulfur-bridged enaminones and chromones via double C(sp 2 )-H thiolation
Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2017 Iodine-catalyzed synthesis of sulfur-bridged enaminones and chromones via
Διαβάστε περισσότεραCopper-Catalyzed Oxidative Coupling of Acids with Alkanes Involving Dehydrogenation: Facile Access to Allylic Esters and Alkylalkenes
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2014 Supplementary information Copper-Catalyzed xidative Coupling of Acids with Alkanes Involving Dehydrogenation:
Διαβάστε περισσότεραSupporting Information
Supporting Information for AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds Qiuping Ding 1, Dan Wang 1, Puying Luo* 2, Meiling Liu 1, Shouzhi Pu* 3 and
Διαβάστε περισσότεραDivergent synthesis of various iminocyclitols from D-ribose
Electronic Supplementary Material (ESI) for rganic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 205 Divergent synthesis of various iminocyclitols from D-ribose Ramu Petakamsetty,
Διαβάστε περισσότεραD-Glucosamine-derived copper catalyst for Ullmann-type C- N coupling reaction: theoretical and experimental study
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2016 D-Glucosamine-derived copper catalyst for Ullmann-type C- N coupling reaction: theoretical
Διαβάστε περισσότεραRh(III)-Catalyzed C-H Amidation with N-hydroxycarbamates: A. new Entry to N-Carbamate Protected Arylamines
Rh(III)-Catalyzed C-H Amidation with N-hydroxycarbamates: A new Entry to N-Carbamate Protected Arylamines Bing Zhou,* Juanjuan Du, Yaxi Yang,* Huijin Feng, Yuanchao Li Shanghai Institute of Materia Medica,
Διαβάστε περισσότεραDirect Palladium-Catalyzed Arylations of Aryl Bromides. with 2/9-Substituted Pyrimido[5,4-b]indolizines
Direct Palladium-Catalyzed Arylations of Aryl Bromides with 2/9-Substituted Pyrimido[5,4-b]indolizines Min Jiang, Ting Li, Linghua Meng, Chunhao Yang,* Yuyuan Xie*, and Jian Ding State Key Laboratory of
Διαβάστε περισσότεραOxyhalogenation of thiols and disulfides into sulfonyl chlorides/ bromides in water using oxone-kx(x= Cl or Br)
Electronic Supplementary Material (ESI) for Green Chemistry. This journal is The Royal Society of Chemistry 2014 Oxyhalogenation of thiols and disulfides into sulfonyl chlorides/ bromides in water using
Διαβάστε περισσότεραSupporting Information One-Pot Approach to Chiral Chromenes via Enantioselective Organocatalytic Domino Oxa-Michael-Aldol Reaction
Supporting Information ne-pot Approach to Chiral Chromenes via Enantioselective rganocatalytic Domino xa-michael-aldol Reaction Hao Li, Jian Wang, Timiyin E-Nunu, Liansuo Zu, Wei Jiang, Shaohua Wei, *
Διαβάστε περισσότεραSupporting Information
Supporting Information 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Convenient and General Zinc-Catalyzed Borylation of Aryl Diazonium Salts and Aryltriazenes under Mild Conditions
Διαβάστε περισσότεραSupporting Information
Supporting Information for Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolecular [1,5]-hydride shift/isomerization reaction Chun-Huan Jiang, Xiantao Lei,
Διαβάστε περισσότεραFluorinative Ring-opening of Cyclopropanes by Hypervalent Iodine Reagents. An Efficient Method for 1,3- Oxyfluorination and 1,3-Difluorination
Electronic Supplementary Material (ESI) for Chemical Science. This journal is The Royal Society of Chemistry 2016 Supporting Information Fluorinative Ring-opening of Cyclopropanes by Hypervalent Iodine
Διαβάστε περισσότεραDirect Transformation of Ethylarenes into Primary Aromatic Amides with N-Bromosuccinimide and I 2 -aq NH 3
Supporting Information Direct Transformation of Ethylarenes into Primary Aromatic Amides with N-Bromosuccinimide and I 2 -aq NH 3 Shohei Shimokawa, Yuhsuke Kawagoe, Katsuhiko Moriyama, Hideo Togo* Graduate
Διαβάστε περισσότεραSupporting Information
Supporting Information Lewis acid catalyzed ring-opening reactions of methylenecyclopropanes with diphenylphosphine oxide in the presence of sulfur or selenium Min Shi,* Min Jiang and Le-Ping Liu State
Διαβάστε περισσότεραSite-Selective Suzuki-Miyaura Cross-Coupling Reactions of 2,3,4,5-Tetrabromofuran
1 Site-Selective Suzuki-Miyaura Cross-Coupling Reactions of 2,3,4,5-Tetrabromofuran Munawar Hussain, a Rasheed Ahmad Khera, a Nguyen Thai Hung, a Peter Langer* a,b a Institut für Chemie, Universität Rostock,
Διαβάστε περισσότεραEnantioselective Organocatalytic Michael Addition of Isorhodanines. to α, β-unsaturated Aldehydes
Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2016 Enantioselective Organocatalytic Michael Addition of Isorhodanines to α,
Διαβάστε περισσότεραphase: synthesis of biaryls, terphenyls and polyaryls
Supporting Information for Studies on Pd/NiFe 2 O 4 catalyzed ligand-free Suzuki reaction in aqueous phase: synthesis of biaryls, terphenyls and polyaryls Sanjay R. Borhade and Suresh B. Waghmode* Address:
Διαβάστε περισσότεραgem-dichloroalkenes for the Construction of 3-Arylchromones
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2015 Pd(OAc)2/S=PPh3 Accelerated Activation of gem-dichloroalkenes for the Construction of 3-Arylchromones
Διαβάστε περισσότεραThe Free Internet Journal for Organic Chemistry
The Free Internet Journal for Organic Chemistry Paper Archive for Organic Chemistry Arkivoc 2018, part iii, S1-S6 Synthesis of dihydropyranones and dihydropyrano[2,3- d][1,3]dioxine-diones by cyclization
Διαβάστε περισσότεραSupporting Information for
Supporting Information for An atom-economic route to densely functionalized thiophenes via base-catalyzed rearrangement of 5-propargyl-2H-thiopyran-4(3H)-ones Chunlin Tang a, Jian Qin b, Xingqi Li *a a
Διαβάστε περισσότεραSupporting Information. Asymmetric Binary-acid Catalysis with Chiral. Phosphoric Acid and MgF 2 : Catalytic
Supporting Information Asymmetric Binary-acid Catalysis with Chiral Phosphoric Acid and MgF 2 : Catalytic Enantioselective Friedel-Crafts Reactions of β,γ- Unsaturated-α-Ketoesters Jian Lv, Xin Li, Long
Διαβάστε περισσότεραSupporting Information
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2015 Synthesis of 3-omosubstituted Pyrroles via Palladium- Catalyzed Intermolecular Oxidative Cyclization
Διαβάστε περισσότεραSynthesis of novel 1,2,3-triazolyl derivatives of pregnane, androstane and D-homoandrostane. Tandem Click reaction/cu-catalyzed D-homo rearrangement
Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2014 Supporting Information Synthesis of novel 1,2,3-triazolyl derivatives of
Διαβάστε περισσότεραSupporting Information
Supporting Information Ceric Ammonium Nitrate (CAN) catalyzed efficient one-pot three component aza-diels-alder reactions for a facile synthesis of tetrahydropyranoquinoline derivatives Ravinder Goud Puligoundla
Διαβάστε περισσότεραSupporting Materials
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2016 Carbonylative Coupling of Aryl Tosylates/triflates with Arylboronic Acids under CO Atmosphere
Διαβάστε περισσότεραProtease-catalysed Direct Asymmetric Mannich Reaction in Organic Solvent
Supplementary information for the paper Protease-catalysed Direct Asymmetric Mannich Reaction in Organic Solvent Yang Xue, Ling-Po Li, Yan-Hong He * & Zhi Guan * School of Chemistry and Chemical Engineering,
Διαβάστε περισσότεραLewis Acid Catalyzed Propargylation of Arenes with O-Propargyl Trichloroacetimidate: Synthesis of 1,3-Diarylpropynes
Supporting Information for Lewis Acid Catalyzed Propargylation of Arenes with O-Propargyl Trichloroacetimidate: Synthesis of 1,3-Diarylpropynes Changkun Li and Jianbo Wang* Beijing National Laboratory
Διαβάστε περισσότεραSupporting information
Electronic upplementary Material (EI) for New Journal of Chemistry. This journal is The Royal ociety of Chemistry and the Centre National de la Recherche cientifique 7 upporting information Lipase catalyzed,-addition
Διαβάστε περισσότεραHiyama Cross-Coupling of Chloro-, Fluoroand Methoxy- pyridyl trimethylsilanes : Room-temperature Novel Access to Functional Bi(het)aryl
Hiyama Cross-Coupling of Chloro-, Fluoroand Methoxy- pyridyl trimethylsilanes : Room-temperature Novel Access to Functional Bi(het)aryl Philippe Pierrat, Philippe Gros* and Yves Fort Synthèse Organométallique
Διαβάστε περισσότεραSupporting Information
Supporting Information Montmorillonite KSF-Catalyzed One-pot, Three-component, Aza-Diels- Alder Reactions of Methylenecyclopropanes With Arylaldehydes and Aromatic Amines Li-Xiong Shao and Min Shi* General
Διαβάστε περισσότεραRegioselectivity in the Stille coupling reactions of 3,5- dibromo-2-pyrone.
Regioselectivity in the Stille coupling reactions of 3,5- dibromo-2-pyrone. Won-Suk Kim, Hyung-Jin Kim and Cheon-Gyu Cho Department of Chemistry, Hanyang University, Seoul 133-791, Korea Experimental Section
Διαβάστε περισσότεραSupporting Information
Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2018 Supporting Information Silver or Cerium-Promoted Free Radical Cascade Difunctionalization
Διαβάστε περισσότερα9-amino-(9-deoxy)cinchona alkaloids-derived novel chiral phase-transfer catalysts
Electronic Supplementary Material (ESI) for Organic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2014 9-amino-(9-deoxy)cinchona alkaloids-derived novel chiral phase-transfer
Διαβάστε περισσότεραFast copper-, ligand- and solvent-free Sonogashira coupling in a ball mill
Electronic Supporting Information Fast copper-, ligand- and solvent-free Sonogashira coupling in a ball mill Rico Thorwirth, Achim Stolle * and Bernd ndruschka Institute for Technical Chemistry and Environmental
Διαβάστε περισσότεραSupporting Information
Electronic Supplementary Material (ESI) for rganic Chemistry Frontiers. This journal is the Partner rganisations 2018 Palladium-catalyzed direct approach to α-cf 3 aryl ketones from arylboronic acids Bo
Διαβάστε περισσότεραRoom Temperature Highly Diastereoselective Zn-Mediated. Allylation of Chiral N-tert-Butanesulfinyl Imines: Remarkable Reaction Condition Controlled
Supporting Information for: Room Temperature Highly Diastereoselective Zn-Mediated Allylation of Chiral N-tert-Butanesulfinyl Imines: Remarkable Reaction Condition Controlled Stereoselectivity Reversal
Διαβάστε περισσότεραNovel and Selective Palladium-Catalyzed Annulation of 2-Alkynylphenols to Form 2-Substituted 3-Halobenzo[b]furans. Supporting Information
Novel and Selective Palladium-Catalyzed Annulation of 2-Alkynylphenols to Form 2-Substituted 3-Halobenzo[b]furans Liang Yun, Shi Tang, Xu-Dong Zhang, Li-Qiu Mao, Ye-Xiang Xie and Jin-Heng Li* Key Laboratory
Διαβάστε περισσότεραSupporting Information. Experimental section
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2014 Supporting Information Experimental section General. Proton nuclear magnetic resonance ( 1
Διαβάστε περισσότεραSupporting information
Electronic Supplementary Material (ESI) for Green Chemistry. This journal is The Royal Society of Chemistry 204 Supporting information Palladium nanoparticles supported on triazine functionalised mesoporous
Διαβάστε περισσότεραSupporting Information
Supporting Information Metal-catalyzed Stereoselective and Protecting-group-free Synthesis of 1,2-cis-Glycosides Using 4,6-Dimethoxy-1,3,5-triazin-2-yl Glycosides as Glycosyl Donors Tomonari Tanaka,* 1
Διαβάστε περισσότεραPhosphorus Oxychloride as an Efficient Coupling Reagent for the Synthesis of Ester, Amide and Peptide under Mild Conditions
Supplementary Information for Phosphorus xychloride as an Efficient Coupling Reagent for the Synthesis of Ester, Amide and Peptide under Mild Conditions u Chen,* a,b Xunfu Xu, a Liu Liu, a Guo Tang,* a
Διαβάστε περισσότεραFirst DMAP-mediated direct conversion of Morita Baylis. Hillman alcohols into γ-ketoallylphosphonates: Synthesis of
Supporting Information File 1 for First DMAP-mediated direct conversion of Morita Baylis Hillman alcohols into γ-ketoallylphosphonates: Synthesis of γ-aminoallylphosphonates Marwa Ayadi 1,2, Haitham Elleuch
Διαβάστε περισσότεραSupporting Information
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2014 Supporting Information A Convenient and Efficient Synthesis of Glycals by Zinc Nanoparticles
Διαβάστε περισσότεραElectronic Supplementary Information
Electronic Supplementary Information NbCl 3 -catalyzed [2+2+2] intermolecular cycloaddition of alkynes and alkenes to 1,3-cyclohexadiene derivatives Yasushi Obora,* Keisuke Takeshita and Yasutaka Ishii*
Διαβάστε περισσότεραCopper-promoted hydration and annulation of 2-fluorophenylacetylene derivatives: from alkynes to benzo[b]furans and benzo[b]thiophenes
Supporting Information for Copper-promoted hydration and annulation of 2-fluorophenylacetylene derivatives: from alkynes to benzo[b]furans and benzo[b]thiophenes Yibiao Li* 1, Liang Cheng 1, Xiaohang Liu
Διαβάστε περισσότεραRhodium-Catalyzed Oxidative Decarbonylative Heck-type Coupling of Aromatic Aldehydes with Terminal Alkenes
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2015 Electronic Supplementary Information Rhodium-Catalyzed Oxidative Decarbonylative Heck-type
Διαβάστε περισσότεραSupporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006
Supporting Information Copyright Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, 2006 1 A Facile Way to Synthesize 2H-Chromenes: Reconsideration of the Reaction Mechanism between Salicylic Aldehyde and
Διαβάστε περισσότεραTributylphosphine-Catalyzed Cycloaddition of Aziridines with Carbon Disulfide and Isothiocyanate
upporting Information Tributylphosphine-Catalyzed Cycloaddition of Aziridines with Carbon Disulfide and Isothiocyanate Jing-Yu Wu, Zhi-Bin Luo, Li-Xin Dai and Xue-Long Hou* a tate Key Laboratory of Organometallic
Διαβάστε περισσότεραSupporting Information
Supporting Information An Approach to 3,6-Disubstituted 2,5-Dioxybenzoquinones via Two Sequential Suzuki Couplings. Three-step Synthesis of Leucomelone Xianwen Gan, Wei Jiang, Wei Wang,,,* Lihong Hu,,*
Διαβάστε περισσότεραSupplementary Data. Engineering, Nanjing University, Nanjing , P. R. China;
Supplementary Data Synthesis, Chemo-selective Properties of Substituted 9-Aryl-9H-fluorenes from Triarylcarbinols and Enantiomerical Kinetics of Chiral 9-Methoxy-11-(naphthalen-1-yl)-11H-benzo[a]fluorene
Διαβάστε περισσότεραSupporting Information
Electronic upplementary Material (EI) for Green Chemistry. This journal is The Royal ociety of Chemistry 204 upporting Information ynthesis of sulfonamides via I 2 -mediated reaction of sodium sulfinates
Διαβάστε περισσότεραSUPPORTING INFORMATION. Polystyrene-immobilized DABCO as a highly efficient and recyclable organocatalyst for Knoevenagel condensation
Electronic Supplementary Material (ESI) for RSC Advances This journal is The Royal Society of Chemistry 213 SUPPORTING INFORMATION Polystyrene-immobilized DABCO as a highly efficient and recyclable organocatalyst
Διαβάστε περισσότεραLigand-free Cu(II)-mediated aerobic oxidations of aldehyde. hydrazones leading to N,N -diacylhydrazines and 1,3,4-oxadiazoles
Electronic Supplementary Material (ESI) for rganic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2017 Ligand-free Cu(II)-mediated aerobic oxidations of aldehyde hydrazones leading
Διαβάστε περισσότεραHighly enantioselective cascade synthesis of spiropyrazolones. Supporting Information. NMR spectra and HPLC traces
Highly enantioselective cascade synthesis of spiropyrazolones Alex Zea a, Andrea-Nekane R. Alba a, Andrea Mazzanti b, Albert Moyano a and Ramon Rios a,c * Supporting Information NMR spectra and HPLC traces
Διαβάστε περισσότεραElectronic Supplementary Information (ESI)
Electronic Supplementary Material (ESI) for rganic & Biomolecular Chemistry Electronic Supplementary Information (ESI) For Iron-Catalysed xidative Amidation of Alcohols with Amines Silvia Gaspa, a Andrea
Διαβάστε περισσότεραSynthesis of Imines from Amines in Aliphatic Alcohols on Pd/ZrO 2 Catalyst at Ambient Conditions
This journal is The Royal Society of Chemistry 213 Synthesis of Imines from Amines in Aliphatic Alcohols on Pd/ZrO 2 Catalyst at Ambient Conditions Wenjing Cui, a Bao Zhaorigetu,* a Meilin Jia, a and Wulan
Διαβάστε περισσότεραSupplementary Material
Supplementary Material Control experiments S2 Characterization data for the products S2-S7 References S8 MR spectra for the products S9-S28 S1 Control experiments 2a (99.5 mg, 0.5 mmol), I 2 (50.8 mg,
Διαβάστε περισσότεραSupporting Information. Experimental section
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2014 Supporting Information Experimental section General. Anhydrous solvents were transferred by
Διαβάστε περισσότεραSupporting Information
Supporting Information Rhodium-catalyzed Intramolecular Dehydrogenative Aryl Aryl Coupling Using Air as Terminal Oxidant Hannah Baars, 1,2 Yuto Unoh, 1 Takeshi Okada, 1 Koji Hirano, 1 Tetsuya Satoh,* 1,3
Διαβάστε περισσότεραPd Catalyzed Carbonylation for the Construction of Tertiary and
Electronic Supplementary Material (ESI) for rganic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 2014 Pd Catalyzed Carbonylation for the Construction of Tertiary and Quaternary
Διαβάστε περισσότεραSupplementary information
Electronic Supplementary Material (ESI) for MedChemComm. This journal is The Royal Society of Chemistry 2015 Supplementary information Synthesis of carboxyimidamide-substituted benzo[c][1,2,5]oxadiazoles
Διαβάστε περισσότεραReusable Cu 2 O/PPh 3 /TBAB System for the Cross-Couplings of Aryl Halides and Heteroaryl Halides with Terminal Alkynes. Supporting Information
Reusable Cu 2 O/PPh 3 /TBAB System for the Cross-Couplings of Aryl Halides and Heteroaryl Halides with Terminal Alkynes Bo-Xiao Tang, Feng Wang, Jin-Heng Li,* Ye-Xiang Xie, and Man-Bo Zhang* Key Laboratory
Διαβάστε περισσότεραSupporting Information for Synthesis of Fused N-Heterocycles via Tandem C-H Activation
This journal is The Royal Society of Chemistry 212 Supporting Information for Synthesis of Fused -Heterocycles via Tandem C-H Activation Ge Meng, Hong-Ying iu, Gui-Rong Qu, John S. Fossey, Jian-Ping Li,*
Διαβάστε περισσότεραSupporting Information for
Supporting Information for Palladium-Catalyzed C-H Bond Functionalization of C6-Arylpurines Hai-Ming Guo,* Wei-Hao Rao, Hong-Ying iu, Li-Li Jiang, Ge ng, Jia-Jia Jin, Xi-ing Yang, and Gui-Rong Qu* College
Διαβάστε περισσότεραFerric(III) Chloride Catalyzed Halogenation Reaction of Alcohols and Carboxylic Acids using - Dichlorodiphenylmethane
Supporting Information Ferric(III) Chloride Catalyzed Halogenation Reaction of Alcohols and Carboxylic Acids using - Dichlorodiphenylmethane Chang-Hee Lee,, Soo-Min Lee,, Byul-Hana Min, Dong-Su Kim, Chul-Ho
Διαβάστε περισσότεραSupporting Information. Microwave-assisted construction of triazole-linked amino acid - glucoside conjugates as novel PTP1B inhibitors
Supporting Information Microwave-assisted construction of triazole-linked amino acid - glucoside conjugates as novel PTP1B inhibitors Xiao-Peng He, abd Cui Li, d Xiao-Ping Jin, b Zhuo Song, b Hai-Lin Zhang,
Διαβάστε περισσότεραVilsmeier Haack reagent-promoted formyloxylation of α-chloro-narylacetamides
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 205 Vilsmeier aack reagent-promoted formyloxylation of α-chloro-arylacetamides by formamide Jiann-Jyh
Διαβάστε περισσότεραThe N,S-Bidentate Ligand Assisted Pd-Catalyzed C(sp 2 )-H. Carbonylation using Langlois Reagent as CO Source. Supporting Information.
Electronic upplementary Material (EI) for rganic & Biomolecular Chemistry. This journal is The Royal ociety of Chemistry 2018 The,-Bidentate Ligand Assisted Pd-Catalyzed C(sp 2 )-H Carbonylation using
Διαβάστε περισσότεραKishore Natte, Jianbin Chen, Helfried Neumann, Matthias Beller, and Xiao-Feng Wu*
Electronic Supplementary Material (ESI) for rganic & Biomolecular Chemistry. This journal is The Royal Society of Chemistry 204 Kishore Natte, Jianbin Chen, Helfried Neumann, Matthias Beller, and Xiao-Feng
Διαβάστε περισσότεραAminofluorination of Fluorinated Alkenes
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2018 Synthesis of ɑ CF 3 and ɑ CF 2 H Amines via Aminofluorination of Fluorinated Alkenes Ling Yang,
Διαβάστε περισσότεραSupporting Information
S1 Supporting Information Benzannulation from Alkyne without tallic Catalysts at Room Temperature to 100 o C Tienan Jin,* Fan Yang and Yoshinori Yamamoto* Department of Chemistry, Graduate School of Science,
Διαβάστε περισσότεραMandelamide-Zinc Catalyzed Alkyne Addition to Heteroaromatic Aldehydes
1 Mandelamide-Zinc Catalyzed Alkyne Addition to Heteroaromatic Aldehydes Gonzalo Blay, Isabel Fernández, Alícia Marco-Aleixandre, and José R. Pedro Departament de Química Orgànica, Facultat de Química,
Διαβάστε περισσότεραSupporting Information for Iron-catalyzed decarboxylative alkenylation of cycloalkanes with arylvinylic carboxylic acids via a radical process
Supporting Information for Iron-catalyzed decarboxylative alkenylation of cycloalkanes with arylvinylic carboxylic acids via a radical process Jincan Zhao 1, Hong Fang 1, Jianlin Han* 1,2 and Yi Pan* 1
Διαβάστε περισσότεραSynthesis and evaluation of novel aza-caged Garcinia xanthones
Electronic Supplementary Material (ESI) for rganic & Biomolecular Chemistry Synthesis and evaluation of novel aza-caged Garcinia xanthones Xiaojin Zhang, a,1 Xiang Li, a,1 Haopeng Sun, * b Zhengyu Jiang,
Διαβάστε περισσότεραFacile construction of the functionalized 4H-chromene via tandem. benzylation and cyclization. Jinmin Fan and Zhiyong Wang*
Facile construction of the functionalized 4H-chromene via tandem benzylation and cyclization Jinmin Fan and Zhiyong Wang* Hefei National Laboratory for Physical Science at Microscale, Joint- Lab of Green
Διαβάστε περισσότεραSotto, 8; Perugia, Italia. Fax: ; Tel: ;
ELECTRONIC SUPPORTING INFORMATION Ermal Ismalaj a, Giacomo Strappaveccia a, Eleonora Ballerini a, Fausto Elisei a, Oriana Piermatti a, Dmitri Gelman b, Luigi Vaccaro a a CEMIN - Dipartimento di Chi mica,
Διαβάστε περισσότεραSupporting Information
Supporting Information Wiley-VC 007 9 Weinheim, Germany ew ear Infrared Dyes and Fluorophores Based on Diketopyrrolopyrroles Dipl.-Chem. Georg M. Fischer, Dipl.-Chem. Andreas P. Ehlers, Prof. Dr. Andreas
Διαβάστε περισσότεραSupplementary Figure S1. Single X-ray structure 3a at probability ellipsoids of 20%.
Supplementary Figure S1. Single X-ray structure 3a at probability ellipsoids of 20%. S1 Supplementary Figure S2. Single X-ray structure 5a at probability ellipsoids of 20%. S2 H 15 Ph Ac Ac I AcH Ph Ac
Διαβάστε περισσότεραSupporting Information
Supporting Information Wiley-VCH 2014 69451 Weinheim, Germany Copper-Catalyzed Coupling of Oxime Acetates with Sodium Sulfinates: An Efficient Synthesis of Sulfone Derivatives** Xiaodong Tang, Liangbin
Διαβάστε περισσότεραSUPPORTING INFORMATION
Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 2016 SUPPORTIG IFORMATIO Visible light-mediated decarboxylative amination of indoline-2- carboxylic
Διαβάστε περισσότεραSupporting Information
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2017 Supporting Information 1. General experimental methods (S2). 2. Table 1: Initial studies (S2-S4).
Διαβάστε περισσότεραSupporting Information
Supporting Information Selective Synthesis of xygen-containing Heterocycles via Tandem Reactions of 1,2-Allenic Ketones with Ethyl 4-Chloroacetoacetate Qiang Wang, a, b Zhouqing Xu b and Xuesen Fan a *
Διαβάστε περισσότεραAluminium-mediated Aromatic C F Bond Activation: Regioswitchable Construction of Benzene-fused Triphenylene. Frameworks
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2016 Aluminium-mediated Aromatic C Bond Activation: Regioswitchable Construction of Benzene-fused Triphenylene
Διαβάστε περισσότεραSupporting Information. for. Highly Selective Hydroiodation of Alkynes Using. Iodine-Hydrophosphine Binary System
Supporting Information for Highly Selective Hydroiodation of Alkynes Using Iodine-Hydrophosphine Binary System Shin-ichi Kawaguchi and Akiya Ogawa * Department of Applied Chemistry, Graduate School of
Διαβάστε περισσότεραEfficient and Simple Zinc mediated Synthesis of 3 Amidoindoles
Electronic Supplementary Material (ESI) for rganic and Biomolecular Chemistry SUPPRTIG IFRMATI Efficient and Simple Zinc mediated Synthesis of 3 Amidoindoles Anahit Pews-Davtyan and Matthias Beller* Leibniz-Institut
Διαβάστε περισσότεραAcylative Suzuki coupling of amides: Acyl-nitrogen activation via synergy of independently modifiable activating groups
Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2015 Supporting Information for Acylative Suzuki coupling of amides: Acyl-nitrogen activation via synergy
Διαβάστε περισσότεραSupplementary material
Electronic Supplementary Material (ESI) for New Journal of Chemistry. This journal is The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2015 Supplementary material Recyclable
Διαβάστε περισσότεραSupporting Information. Table of Contents. II. Experimental procedures. II. Copies of 1H and 13C NMR spectra for all compounds
Electronic upplementary Material (EI) for rganic & Biomolecular Chemistry. This journal is The Royal ociety of Chemistry 2017 Laboratoire de Méthodologie et ynthèse de Produit aturels. Université du Québec
Διαβάστε περισσότεραSupplementary Information for
Supplementary Information for Organocatalytic Asymmetric Intramolecular [3+2] Cycloaddition: A Straightforward Approach to Access Multiply Substituted Hexahydrochromeno[4,3-b]pyrrolidine Derivatives in
Διαβάστε περισσότεραSupporting Information
Supporting Information Metal-Free Direct Intramolecular Carbotrifluoromethylation of Alkenes to Functionalized Trifluoromethyl Azaheterocycles Lei Li, Min Deng, Sheng-Cai Zheng, Ya-Ping Xiong, Li-Jiao
Διαβάστε περισσότερα