Supporting Information

Σχετικά έγγραφα
Supporting information

SUPPLEMENTARY DATA. Waste-to-useful: Biowaste-derived heterogeneous catalyst for a green and sustainable Henry reaction

College of Life Science, Dalian Nationalities University, Dalian , PR China.

Copper-Catalyzed Oxidative Dehydrogenative N-N Bond. Formation for the Synthesis of N,N -Diarylindazol-3-ones

Electronic Supplementary information

A facile and general route to 3-((trifluoromethyl)thio)benzofurans and 3-((trifluoromethyl)thio)benzothiophenes

Supporting Information

Supporting Information

Supporting Information

Copper-catalyzed formal O-H insertion reaction of α-diazo-1,3-dicarb- onyl compounds to carboxylic acids with the assistance of isocyanide

The Free Internet Journal for Organic Chemistry

Iodine-catalyzed synthesis of sulfur-bridged enaminones and chromones via double C(sp 2 )-H thiolation

Supporting Information. Experimental section

Supporting Information

Metal-free Oxidative Coupling of Amines with Sodium Sulfinates: A Mild Access to Sulfonamides

9-amino-(9-deoxy)cinchona alkaloids-derived novel chiral phase-transfer catalysts

Novel electroluminescent donor-acceptors based on dibenzo[a,c]phenazine as

Divergent synthesis of various iminocyclitols from D-ribose

Heterobimetallic Pd-Sn Catalysis: Michael Addition. Reaction with C-, N-, O-, S- Nucleophiles and In-situ. Diagnostics

Lewis Acid Catalyzed Propargylation of Arenes with O-Propargyl Trichloroacetimidate: Synthesis of 1,3-Diarylpropynes

Supporting Information One-Pot Approach to Chiral Chromenes via Enantioselective Organocatalytic Domino Oxa-Michael-Aldol Reaction

Supporting Information

Electronic Supplementary Information. Carbon dioxide as a reversible amine-protecting

phase: synthesis of biaryls, terphenyls and polyaryls

Electronic Supplementary Information

Supplementary Figure S1. Single X-ray structure 3a at probability ellipsoids of 20%.

Supporting Information. Experimental section

Supporting Information

Facile construction of the functionalized 4H-chromene via tandem. benzylation and cyclization. Jinmin Fan and Zhiyong Wang*

Extended dissolution studies of cellulose in imidazolium based ionic liquids

Protease-catalysed Direct Asymmetric Mannich Reaction in Organic Solvent

Synthesis of Imines from Amines in Aliphatic Alcohols on Pd/ZrO 2 Catalyst at Ambient Conditions

Heavier chalcogenone complexes of bismuth(iii)trihalides: Potential catalysts for acylative cleavage of cyclic ethers. Supporting Information

Supplementary material

Vilsmeier Haack reagent-promoted formyloxylation of α-chloro-narylacetamides

Site-Selective Suzuki-Miyaura Cross-Coupling Reactions of 2,3,4,5-Tetrabromofuran

Eco-friendly synthesis of diverse and valuable 2-pyridones by catalyst- and solvent-free thermal multicomponent domino reaction

Highly enantioselective cascade synthesis of spiropyrazolones. Supporting Information. NMR spectra and HPLC traces

Supporting Information

Supporting Information. Asymmetric Binary-acid Catalysis with Chiral. Phosphoric Acid and MgF 2 : Catalytic

Supporting Information

ESI for. A simple and efficient protocol for the palladium-catalyzed. ligand-free Suzuki reaction at room temperature in aqueous DMF.

Nitric oxide (NO) reactivity studies on mononuclear Iron(II) complexes supported by a tetradentate Schiff base Ligand

Supporting Information Synthesis of cyclometalated 1,3,5-triphenylpyrazole palladium dimer and its activity towards cross coupling reactions

SUPPLEMENTARY MATERIAL

Free Radical Initiated Coupling Reaction of Alcohols and. Alkynes: not C-O but C-C Bond Formation. Context. General information 2. Typical procedure 2

The N,S-Bidentate Ligand Assisted Pd-Catalyzed C(sp 2 )-H. Carbonylation using Langlois Reagent as CO Source. Supporting Information.

Supporting Information

Electronic Supplementary Information

Regioselectivity in the Stille coupling reactions of 3,5- dibromo-2-pyrone.

Supporting Information. Introduction of a α,β-unsaturated carbonyl conjugated pyrene-lactose hybrid

Enantioselective Organocatalytic Michael Addition of Isorhodanines. to α, β-unsaturated Aldehydes

gem-dichloroalkenes for the Construction of 3-Arylchromones

Phosphorus Oxychloride as an Efficient Coupling Reagent for the Synthesis of Ester, Amide and Peptide under Mild Conditions

Kishore Natte, Jianbin Chen, Helfried Neumann, Matthias Beller, and Xiao-Feng Wu*

Direct Transformation of Ethylarenes into Primary Aromatic Amides with N-Bromosuccinimide and I 2 -aq NH 3

Supporting Information

Rhodium-Catalyzed Oxidative Decarbonylative Heck-type Coupling of Aromatic Aldehydes with Terminal Alkenes

Supporting information

Fast copper-, ligand- and solvent-free Sonogashira coupling in a ball mill

Supplementary!Information!

Electronic Supplementary Information

Supporting Information. Palladium Complexes with Bulky Diphosphine. Synthesis of (Bio-) Adipic Acid from Pentenoic. Acid Mixtures.

D-Glucosamine-derived copper catalyst for Ullmann-type C- N coupling reaction: theoretical and experimental study

Supporting Information. for. Highly Selective Hydroiodation of Alkynes Using. Iodine-Hydrophosphine Binary System

Supporting Information for Iron-catalyzed decarboxylative alkenylation of cycloalkanes with arylvinylic carboxylic acids via a radical process

Sotto, 8; Perugia, Italia. Fax: ; Tel: ;

Direct Palladium-Catalyzed Arylations of Aryl Bromides. with 2/9-Substituted Pyrimido[5,4-b]indolizines

Table of Contents 1 Supplementary Data MCD

using metal-organic framework Cu-MOF-74 as an efficient heterogeneous catalyst Hanh T. H. Nguyen, Oanh T. K. Nguyen, Thanh Truong *, Nam T. S.

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006

Hiyama Cross-Coupling of Chloro-, Fluoroand Methoxy- pyridyl trimethylsilanes : Room-temperature Novel Access to Functional Bi(het)aryl

Supplement: Intramolecular N to N acyl migration in conformationally mobile 1 -acyl-1- systems promoted by debenzylation conditions (HCOONH 4

Supporting Information

Supporting Information

Novel and Selective Palladium-Catalyzed Annulation of 2-Alkynylphenols to Form 2-Substituted 3-Halobenzo[b]furans. Supporting Information

Efficient and Simple Zinc mediated Synthesis of 3 Amidoindoles

Room Temperature Highly Diastereoselective Zn-Mediated. Allylation of Chiral N-tert-Butanesulfinyl Imines: Remarkable Reaction Condition Controlled

SUPPORTING INFORMATION. Polystyrene-immobilized DABCO as a highly efficient and recyclable organocatalyst for Knoevenagel condensation

Supporting information

Available online at

Supplementary Information

Supporting Information

An experimental and theoretical study of the gas phase kinetics of atomic chlorine reactions with CH 3 NH 2, (CH 3 ) 2 NH, and (CH 3 ) 3 N

Mandelamide-Zinc Catalyzed Alkyne Addition to Heteroaromatic Aldehydes

Synthesis of novel 1,2,3-triazolyl derivatives of pregnane, androstane and D-homoandrostane. Tandem Click reaction/cu-catalyzed D-homo rearrangement

Supplementary Information for

Electronic Supplementary Information

Supporting Information. for

Supporting Information. A catalyst-free multicomponent domino sequence for the. diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-

Supplementary Materials: Development of Amyloseand β-cyclodextrin-based Chiral Fluorescent Sensors Bearing Terthienyl Pendants

Supporting Information for

Bishwajit Saikia*, Preeti Rekha Boruah, Abdul Aziz Ali and Diganta Sarma. Contents

Fluorinative Ring-opening of Cyclopropanes by Hypervalent Iodine Reagents. An Efficient Method for 1,3- Oxyfluorination and 1,3-Difluorination

Supporting Information

Supporting Information. Consecutive hydrazino-ugi-azide reactions: synthesis of acylhydrazines bearing 1,5- disubstituted tetrazoles

Supporting Information

Supporting information. An unusual bifunctional Tb-MOF for highly sensing of Ba 2+ ions and remarkable selectivities of CO 2 /N 2 and CO 2 /CH 4

Copper-promoted hydration and annulation of 2-fluorophenylacetylene derivatives: from alkynes to benzo[b]furans and benzo[b]thiophenes

Supporting Information

Transcript:

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 2017 Supporting Information Palladium nanoparticles immobilized on a magnetic Chitosan-anchored Schiff base: Application in Suzuki-Miyaura and Heck-Mizoroki coupling reactions Anuradha a, Shweta Kumari b, Samaresh Layek a, and Devendra D. Pathak a* a Department of Applied Chemistry, Indian Institute of Technology (ISM), Dhanbad-826004, India b Department of Chemical Engineering, Indian Institute of Technology, Gandhinagar-382355, India Email: anuradhakumar3107@gmail.com (Anuradha), shweta@ac.ism.ac.in (Shweta Kumari), samareshchemist92@gmail.com (Samaresh Layek). ddpathak@yahoo.com * * Phone number: +91 9431126250

Contents Page No. 1. Instrumentation 3 2. Fig. S1. Reusability of the catalyst in Suzuki-Miyaura coupling reaction 3 3. Fig. S2. Reusability of the catalyst in Heck-Mizoroki coupling reaction 4 4. Fig. S3. FT-IR of reusable Fe 3 O 4 @CS-SB-Pd nanocatalyst after 5 th cycle 4 5. Fig. S4. FESEM image and EDX analysis of Fe 3 O 4 @CS-SB-Pd nanocatalyst after 5 th cycle 4 6. Spectral data of Suzuki-Miyaura coupling product 5-7 7. 1 H and 13 C NMR Spectra of Suzuki-Miyaura coupling product (Fig. S5-S26) 7-18 8. Spectral data of Heck-Mizoroki coupling product 18-20 9. 1 H and 13 C NMR Spectra of Heck-Mizoroki coupling product (Fig. S27-S44) 20-29

Instrumentation FT-IR spectra were recorded using KBr pellets on a Perkin Elmer Spectrometer in the range of 4000-400 cm -1. The powder X-ray diffraction (XRD) analysis of catalyst was carried out using a Bruker D8 Advance diffractometer at 40 kv and 40 ma with CuKα radiation (λ=0.15418 nm). XPS spectrum of the catalyst was recorded using model PHI 5000 Versa Prob II, FEI Inc. The surface morphology was characterized by Field Emission Scanning Electron Microscope (FESEM) of model FESEM Supra 55 (Carl Zeiss, Germany) with the accelerating voltage of 20kv at liquid nitrogen atmosphere. The EDX analysis was carried out using Electron Backscatter Diffraction (Oxford Integrated Advanced Aztec HKL EBSD with Forescatter system with 4 diodes for Nordlys Analysis. TEM of a nanocatalyst was carried out using model Jeol/JEM 2100. Thermo gravimetric analyses (TGA) were performed on a NETZSCH, STA 449 F3 Jupiter in the temperature range of 0-600 C with heating ramp of 10 C min -1 under nitrogen flow. Palladium content in the nanocatalyst was determined by using ICP-AES (Thermo slectron IRIS Intrepid). 1 H and 13 C NMR spectra of the isolated products were recorded on a Bruker Avance-II HD-400 MHz spectrometer in CDCl 3 using TMS as the internal Standard. Br B(OH) 2 OCH 3 + Fe 3 O 4 @CS-SB-Pd K 2 CO 3, PEG-200:H 2 O, 30 min, 50 o C first recycle 99% second recycle 97% third recyle fourth recycle fifth recycle 96% 93% 90% H 3 CO Fig. S1: Recyclability of Suzuki-Miyaura coupling reaction.

Br + Fe 3 O 4 @CS-SB-Pd (0.2 mol%) Et 3 N, PEG-200, 40 min, 120 o C first recycle 98% second recycle 95% third recyle 93% fourth recycle 90% fifth recycle 89% Fig. S2: Recyclability of Heck-Mizoroki coupling reaction. Fig. S3. FT-IR of reusable Fe 3 O 4 @CS-SB-Pd nanocatalyst after 5 th cycle. Fig. S4. FESEM image and EDX analysis of Fe 3 O 4 @CS-SB-Pd nanocatalyst after 5 th cycle.

Spectral data ( 1 H and 13 C NMR) of Isolated Suzuki coupling product: Biphenyl (3a): 1 H NMR (400 MHz, CDCl3): δ = 7.60-7.58 (d, 2H), 7.44-7.46 (d, 2H), 7.35-7.42 (m, 1H), 13 C NMR (CDCl3, 100 MHz): 141.26, 128.82, 127.26, 127.18, 77.34, 77.02, 76.70. H 3 CO 4-methoxy phenyl napthalene (3b): 1 H NMR (400 MHz, CDCl3): δ = 7.99 (s, 1H), 7.90-7.84 (m, 3H), 7.73-7.70 (d, 1H), 7.67-7.66 (m, 2H), 7.53-7.44 (m, 2H), 7.04-7.01 (2H, m), 3.88 (s, 3H). H 3 COC 4-acetyl biphenyl (3c): 1 H NMR (400 MHz, CDCl3): δ = 8.04-8.02 (d, 2H), 7.70-7.68 (d, 2H), 7.64-7.62 (d, 2H), 7.49-7.47 (d, 2H), 7.38-7.45 (m, 1H), 2.64 (s, 1H). H 3 CO OCH 3 4,4-dimethoxy biphenyl (3e): 1 H NMR (400 MHz, CDCl3): δ = 7.49-7.46 (d, 2H), 6.95-6.93(d, 2H), 3.80 (s, 1H). H 3 CO CH 3 4-methoxy-4-methyl biphenyl (3f): 1 H NMR (400 MHz, CDCl3): δ = 7.53-7.51 (d, 2H), 7.40-7.28 (m, 3H), 7.13-7.11 (d, 1H), 6.98-6.96 (d, 2H), 3.85 (s, 3H), 2.41 (s, 3H), 13 C NMR (CDCl3, 100 MHz): 159.79, 138.09, 136.36, 133.76, 129.50, 128.03, 126.59, 114.25, 77.33, 77.01, 76.70, 55.71, 21.07. CH 2 CH 3 4-ethyl biphenyl (3g): 1 H NMR (400 MHz, CDCl3): δ = 7.59-7.57 (d, 2H), 7.53-7.51 (d, 2H), 7.49-7.42 (m, 2H), 7.40-7.32 (m, 1H), 7.28-7.25 (m, 2h), 2.72-2.66 (m, 2H), 1.30-1.26 (t, 3H). OCH 3

4-methoxy biphenyl (3h): 1 H NMR (400 MHz, CDCl3): δ = 7.56-7.43 (m, 4H), 7.42-7.40 (d, 2H), 7.32-7.28 (m, 1H), 6.99-6.97 (d, 2H), 3.88 (s, 3H). 13 C NMR (CDCl3, 100 MHz): 159.79, 133.80, 128.67, 128.09, 126.74, 126.66, 114.63, 77.33, 77.01, 76.69, 55.71. H 3 CO CH 2 CH 3 4-methoxy-4-ethyl biphenyl (3i): 1 H NMR (400 MHz, CDCl3): δ = 7.52 (d, 1H), 7.50 (d, 1H), 7.48 (d, 1H), 7.46 (d, 1H), 7.26 (d, 1H), 7.24 (d, 1H), 6.97 (d, 1H), 6.95 (d, 1H), 3.84 (s, 3H). 2.71-2.65 (m, 2H), 1.29-1.25 (t, 3H). 13 C NMR (CDCl3, 100 MHz): 159.79, 133.80, 128.67, 128.09, 126.74, 126.66, 114.63, 77.33, 77.01, 76.69, 55.71. CH 3 3-methyl biphenyl (3j): 1 H NMR (400 MHz, CDCl3): 7.59-7.57 (d, 2H), 7.45-7.35 (m, 4H), 7.33-7.30 (m, 2H), 7.17-1.14 (t, 1H), 2.42 (s, 3H), 13 C NMR (CDCl3, 100 MHz): 159.43, 140.98, 138.53, 133.91, 128.84, 128.12, 127.57, 127.23, 123.90, 77.33, 77.01, 76.70, 21.66. Cl 4-Chloro biphenyl (3k): 13 C NMR (CDCl3, 100 MHz): 140.01, 139.73, 133.38, 128.95, 128.88, 128.39, 127.59, 126.99, 77.33, 77.01, 76.69. CN 3-cyano biphenyl (3l): 1 H NMR (400 MHz, CDCl3): δ = 7.51-7.49 (d, 2H), 7.42-7.40 (d, 2H), 7.37-7.35 (d, 2H), 7.22-7.08 (m, 1H), 7.07-7.05 (d, 2H). H 3 CO Cl 4-methoxy-4-chloro biphenyl (3m): 1 H NMR (400 MHz, CDCl3): δ = 7.50-7.45 (m, 4H), 7.38-7.36 (d, 2H), 6.98 (d, 1H), 6.96 (d, 1H), 3.85 (s, 3H). 13 C NMR (CDCl3, 100 MHz): 159.43, 133.92, 128.84, 128.09, 126.74, 114.63, 77.46, 77.01, 76.69, 55.71. H 3 CO F 4-methoxy-4-fluoro biphenyl (3n): 1 H NMR (400 MHz, CDCl3): δ = 7.50-7.45 (m, 4H), 7.11-7.09 (m, 2H), 6.97-6.95 (m, 2H), 3.84 (s, 3H). 13 C NMR (CDCl3, 100 MHz): 159.12, 137.08, 132.76, 128.26, 128.18, 128.04, 127.74, 114.26, 114.17, 77.34, 77.02, 76.70, 55.36.

OHC 4-formyl phenyl napthalene (3o): 1 H NMR (400 MHz, CDCl3): δ = 10.13 (s, 1H), 8.03-8.01 (d, 2H), 7.94-7.91 (t, 2H), 7.85-7.83 (d, 1H), 7.69-7.67 (d, 2H), 7.57-7.51 (m, 2H), 7.46-7.43 (m, 2H). N 2-phenyl pyridine (3q): 1 H NMR (400 MHz, CDCl3): δ = 8.71-8.69 (d, 1H), 8.00-7.98 (2H, d), 7.75-7.72 (2H, m), 7.50-7.45 (2H, m), 7.43-7.40 (1H, m), 7.24-7.21 (1H, m) 1 H and 13 C NMR Spectra of Suzuki-Miyaura coupling product: Fig. S5: 1 H NMR of Biphenyl (3a)

Fig. S6: 13 C NMR of Biphenyl (3a) Fig. S7: 1 H NMR of 4-methoxy phenyl napthalene (3b)

Fig. S8: 13 C NMR of 4-methoxy phenyl napthalene (3b) Fig. S9: 1 H NMR of 4-acetyl biphenyl (3c)

Fig. S10: 1 H NMR of of 4,4-dimethoxy biphenyl (3e) Fig. S11: 1 H NMR of 4-methoxy-4-methyl biphenyl (3f)

Fig. S12: 13 C NMR of 4-methoxy-4-methyl biphenyl (3f) Fig. S13: 1 H NMR of 4-ethyl biphenyl (3g)

Fig. S14: 1 H NMR of 4-methoxy biphenyl (3h) Fig. S15: 13 C NMR of 4-methoxy biphenyl (3h)

Fig. S16: 1 H NMR of 4-methoxy-4-ethyl biphenyl (3i) Fig. S17: 1 H NMR of 3-methyl biphenyl (3j)

Fig. S18: 13 C NMR of 3-methyl biphenyl (3j) Fig. S19: 13 C NMR of 4-Chloro biphenyl (3k)

Fig. S20: 1 H NMR of 4-cyano biphenyl (3l) Fig. S21: 1 H NMR of 4-methoxy-4-chloro biphenyl (3m)

Fig. S22: 13 C NMR of 4-methoxy-4-chloro biphenyl (3m) Fig. S23: 1 H NMR of 4-methoxy-4-flouro biphenyl (3n)

Fig. S24: 13 C NMR of 4-methoxy-4-flouro biphenyl (3n) Fig. S25: 1 H NMR of 4-formyl phenyl napthalene (3o)

Fig. S26: 1 H NMR of 2-phenyl pyridine (3q) Spectral data ( 1 H and 13 C NMR) of Heck-Mizoroki coupling product trans-stilbene (3a): 1 H NMR (400 MHz, CDCl3): δ = 7.53-7.51 (d, 2H), 7.37-7.35 (d, 2H), 7.28-7.24 (m, 1H), 7.12 (s, 1H), 13 C NMR (CDCl3, 100 MHz): 137.35, 128.69, 127.62, 126.52, 77.33, 77.02, 76.70. CH 3 4-methyl-trans-stilbene (3b): 1 H NMR (400 MHz, CDCl3): δ = 7.44-7.42 (d, 2H), 7.35-7.33 (d, 2H), 7.29-7.27 (d, 2H), 7.19-7.15 (m, 1H), 7.10-7.08 (d, 2H), 7.00-6.99 (s, 2H), 2.28 (s, 3H), 13 C

NMR (CDCl3, 100 MHz): 137.53, 134.57, 129.48, 128.66, 128.64, 127.72, 127.41, 126.43, 126.40, 77.33, 77.02, 76.70, 21.34. CH 2 Cl 4-chloromethylene trans-stilbene (3c): 1 H NMR (400 MHz, CDCl3): δ = 7.89-7.87 (d, 2H), 7.67-7.65 (d, 2H), 7.57-7.51 (m, 3H), 7.41-7.39 (d, 2H), 7.37-7.35 (d, 1H), 7.13-7.11 (d, 1H), 5.21 (s, 2H), 13 C NMR (CDCl3, 100 MHz): 137.53, 134.57, 129.40, 128.66, 127.77, 127.41, 126.43, 77.33, 77.02, 76.70, 21.93. CH 3 H 3 COC 4-acetyl-4-methyl trans-stilbene (3d): 13 C NMR (CDCl3, 100 MHz): 197.82, 142.29, 138.39, 135.78, 133.95, 131.45, 129.59, 128.88, 126.76, 126.52, 126.39, 77.33, 77.01, 76.99, 26.92, 21.44. H 3 CO 4-methoxy trans-stilbene (3e): 1 H NMR (400 MHz, CDCl3): δ = 7.49-7.43 (m, 3H), 7.35-7.33 (d, 2H), 7.31-7.20 (m, 2H), 7.08-7.04 (d, 1H), 6.98-6.94 (d, 1H), 6.90-6.88 (d, 2H), 3.82 (s, 3H), 13 C NMR (CDCl3, 100 MHz): 159.46, 137.70, 128.72, 128.27, 127.58, 127.21, 126.64, 126.31, 114.20, 77.33, 77.01, 76.69, 55.44. CH 3 H 3 CO 4-methoxy-4-methyl trans-stilbene (3f): 1 H NMR (400 MHz, CDCl3): δ = 7.44-7.42 (d, 2H), 7.39-7.37 (d, 2H), 7.15-7.13 (d, 2H), 7.03-6.99 (d, 1H), 6.96-6.92 (d, 1H), 6.89-6.87 (d, 2H), 3.82 (s, 3H), 2.34 (s, 3H), 13 C NMR (CDCl3, 100 MHz): 159.43, 137.22, 130.36, 129.36, 127.26, 126.59, 126.16, 114.12, 77.33, 77.01, 76.70, 55.36, 21.37. H 3 CO COOCH 3 (E)-methyl 3-(4-methoxyphenyl) acrylate (3g): 13 C NMR (CDCl3, 100 MHz): 168.18, 144.75, 133.45, 129.73, 127.23, 115.95, 114.25, 77.33, 77.01, 76.69. H 3 COC COOCH 3

(E)-methyl 3-(4-acetylphenyl) acrylate (3h) 1 H NMR (400 MHz, CDCl3): δ = 7.98-7.96 (d, 2H), 7.73-7.69 (d, 1H), 7.62-7.60 (d, 2H), 6.55-6.48 (d, 1H), 3.84 (s, 3H), 2.64 (s, 3H), 13 C NMR (CDCl3, 100 MHz): 197.45, 167.31, 143.06, 139.29, 137.69, 129.31, 128.09, 126.57, 77.33, 77.01, 76.69, 51.95, 26.54. OHC COOCH 3 (E)-methyl 3-(4-formylphenyl) acrylate (3i): 1 H NMR (400 MHz, CDCl3): δ = 10.04, (s, 1H), 7.92-7.90 (d, 2H), 7.74-7.67 (m, 3H), 6.58-6.54 (d, 1H), 3.86 (s, 3H), 13 C NMR (CDCl3, 100 MHz): 191.51, 167.35, 143.53, 139.76, 137.69, 130.54, 128.84, 121.40, 77.34, 77.02, 76.70, 51.96. CH 3 OHC 4-formyl-4-methyl trans-stilbene (3j): 1 H NMR (400 MHz, CDCl3): δ = 9.97, (s, 1H), 7.86-7.84 (d, 2H), 7.647.62(d, 2H), 7.44-7.42 (d, 2H), 7.19-7.17 (d, 2H), 7.10-7.06 (d, 2H), 2.36 (s, 3H). N 2-Styryl pyridine (3k): 1 H NMR (400 MHz, CDCl3): δ = 8.69-8.68 (d, 1H), 8.41-8.39 (d, 1H), 7.84-7.76 (m, 4H), 7.38-7.30 (m, 3H), 7.19-7.15 (m, 1H), 7.12-7.07 (m, 1H). 1 H and 13 C NMR Spectra of Heck-Mizoroki coupling product: Fig. S27: 1 H NMR of trans-stilbene (3a)

Fig. S28: 13 C NMR of trans-stilbene (3a) Fig. S29: 1 H NMR of 4-methyl trans-stilbene (3b)

Fig. S30: 13 C NMR of 4-methyl trans-stilbene (3b) Fig. S31: 1 H NMR of 4-chloromethylene trans-stilbene (3c)

Fig. S32: 13 C NMR of 4-chloromethylene trans-stilbene (3c) Fig. S33: 13 C NMR of 4-acetyl-4-methyl trans-stilbene (3d)

Fig. S34: 1 H NMR of 4-methoxy trans-stilbene (3e) Fig. S35: 13 C NMR of 4-methoxy trans-stilbene (3e)

Fig. S36: 1 H NMR of 4-methoxy-4-methyltrans-stilbene (3f) Fig. S37: 13 C NMR of 4-methoxy-4-methyltrans-stilbene (3f)

Fig. S38: 13 C NMR of (E)-methyl 3-(4-methoxyphenyl) acrylate (3g) Fig. S39: 1 H NMR of (E)-methyl 3-(4-acetylphenyl) acrylate (3h)

Fig. S40: 13 C NMR of (E)-methyl 3-(4-acetylphenyl) acrylate (3h) Fig. S41: 1 H NMR of (E)-methyl 3-(4-formylphenyl) acrylate (3i)

Fig. S42: 13 C NMR of (E)-methyl 3-(4-formylphenyl) acrylate (3i) Fig. S43: 1 H NMR of 4-formyl-4-methyl trans-stilbene (3j)

Fig. S44: 1 H NMR of 2-styryl pyridine (3k)