Supporting Information

Similar documents
Enantioselective Conjugate Addition of 3-Fluoro-Oxindoles to. Vinyl Sulfone: An Organocatalytic Access to Chiral. 3-Fluoro-3-Substituted Oxindoles

Supporting Information Carbene-Catalyzed Dynamic Kinetic Resolution of Carboxylic Esters. Table of Contents

Supporting Information 1. Rhodium-catalyzed asymmetric hydroalkoxylation and hydrosufenylation of diphenylphosphinylallenes

Supporting Information

Supporting Information

A Highly Chemoselective and Enantioselective Aza-Henry Reaction of Cyclic -Carbonyl Ketimines under Bifunctional Catalysis

Poly(4-vinylimidazolium)s: A Highly Recyclable Organocatalyst Precursor for. Benzoin Condensation Reaction

for Brønsted Base-Mediated Aziridination of 2- Alkyl Substituted-1,3-Dicarbonyl Compounds and 2-Acyl-1,4-Dicarbonyl Compounds by Iminoiodanes

Supporting Information

Zn-Catalyzed Diastereo- and Enantioselective Cascade. Reaction of 3-Isothiocyanato Oxindoles and 3-Nitroindoles:

Supplementary information

Supporting Information

Organocatalytic asymmetric synthesis of 3,3-disubstituted oxindoles featuring two heteroatoms at C3 position

Electronic Supplementary Material (ESI) for Chemical Communications This journal is The Royal Society of Chemistry 2012

Synthesis of Trifluoromethylated Naphthoquinones via Copper-Catalyzed. Cascade Trifluoromethylation/Cyclization of. 2-(3-Arylpropioloyl)benzaldehydes

Supplementary information

Hualong Ding, Songlin Bai, Ping Lu,* Yanguang Wang*

Brønsted Base-Catalyzed Reductive Cyclization of Alkynyl. α-iminoesters through Auto-Tandem Catalysis

Supporting Information:

Supporting Information

Silver-catalyzed decarboxylative acylfluorination of styrenes in aqueous media

Supporting Information

Singapore, #05 01, 28 Medical Drive, Singapore. PR China,

Supporting Information

Supporting Information. Cu(I)-Catalyzed Three-Component Reaction of Diazo. Compound with Terminal Alkyne and Nitrosobenzene for

Copper(I)/TF-Biphamphos Catalyzed Asymmetric Nitroso. Diels-Alders Reaction

Supporting Information

Suzuki-Miyaura Coupling of Heteroaryl Boronic Acids and Vinyl Chlorides

A Mild, Catalytic and Highly Selective Method for the Oxidation of α,β- Enones to 1,4-Enediones. Jin-Quan Yu, a and E. J.

Supporting Information for. Silver-catalyzed intramolecular hydroamination of alkynes in

Selective Formation of Benzo[c]cinnoline by Photocatalytic Reduction of 2,2 Dinitrobiphenyl with TiO 2 and UV light irradiation

Supporting information for A simple copper-catalyzed two-step one-pot synthesis of indolo[1,2-a]quinazoline

Carbonylative Coupling of Allylic Acetates with. Arylboronic Acids

Lewis-Acid Catalysed One Pot Synthesis of Substituted Xanthenes. Supporting Information

SUPPORTING INFORMATION

Supporting Information. Enantioselective Organocatalyzed Henry Reaction with Fluoromethyl Ketones

Organocatalytic Doubly Annulative Approach to 3,4-Dihydrocoumarins Bearing a Fused Pyrrolidine Scaffold. Dorota Kowalczyk, and Łukasz Albrecht*

Construction of Vicinal Quaternary Carbon Centers via Cobalt- Catalyzed Asymmetric Reverse Prenylation

Palladium-Catalyzed Asymmetric [3+2] Cycloaddition to Construct 1,3-Indandione and Oxindole-Fused Spiropyrazolidine Scaffolds

Supporting Information

SUPPORTING INFORMATION. Fathi Elwrfalli, Yannick J. Esvan, Craig M. Robertson and Christophe Aïssa

A protecting group-free synthesis of the Colorado potato

Supporting Information

SUPPORTING INFORMATION

Supporting Information

Palladium-Catalyzed Oxidative Cyclization of Tertiary Enamines for Synthesis of 1,3,4-Trisubstituted Pyrroles and 1,3-Disubstituted Indoles

Highly Enantioselective hydrosilylation of N-(1,2-diarylethylidene) arylamines

guanidine bisurea bifunctional organocatalyst

Total Synthesis of Gonytolides C and G, Lachnone C, and. Formal Synthesis of Blennolide C and Diversonol

Enantioselective Synthesis of Fused Heterocycles with Contiguous Stereogenic Centers by Chiral Phosphoric Acid-Catalyzed Symmetry Breaking

Copper-Catalyzed Asymmetric Ring Opening of Oxabicyclic Alkenes with Organolithium Reagents

Synthesis of Glaucogenin D, a Structurally Unique. Disecopregnane Steroid with Potential Antiviral Activity

Tetrahydrofuran (THF) was distilled from benzophenone ketyl radical under an argon

Supporting Information - I: Experimental Procedures and Characterization

Table of Contents 1. General procedure for the chiral phosphoric acid catalyzed asymmetric reductive amination using benzothiazoline

Supporting Information. Indole Synthesis via Cobalt(III)-Catalyzed Oxidative Coupling of N-Arylureas and Internal Alkynes

Supporting Information. Molecular Iodine-Catalyzed Aerobic α,β-diamination of Cyclohexanones with 2- Aminopyrimidine and 2-Aminopyridines

Supporting Information

Electronic Supplementary Information for. A Redox-Nucleophilic Dual-Reactable Probe for Highly Selective

SYNTHESIS OF A 3-THIOMANNOSIDE

A Facile and General Approach to 3-((Trifluoromethyl)thio)- 4H-chromen-4-one

Supporting Information

Biobased solvents for the Baylis-Hillman reaction of HMF

Supporting Information

Bulletin of the Chemical Society of Japan

Synergistic Cu/Ir Catalysis. Table of Contents

Supporting Information

Supporting Information

Iron Catalyzed Cross Couplings of Azetidines: Application to an Improved Formal Synthesis of a Pharmacologically Active Molecule

Hai-Bin Yang, Xing Fan, Yin Wei,* Min Shi*

Tuning Porosity and Activity of Microporous Polymer Network Organocatalysts by Co-Polymerisation

Supporting Information

Light irradiation experiments with coumarin [1]

Supporting Information

Regioselective Silylation of Pyranosides Using a Boronic Acid / Lewis Base Co-Catalyst System

Supporting Information

Catalytic Conversion of Diazocarbonyl Compounds to Ketocarbonyl Compounds by 2,6-Dichloropyridine-N-oxide. China Corresponding Author

Enantioselectivity switch in copper-catalyzed conjugate addition. reaction under influence of a chiral N-heterocyclic carbene-silver complex

Supplementary Figure 1. 1 H and 13 C NMR spectra for compound 1a

Supplementary Materials for

*Corresponding author. Tel.: , ; fax: ; Materials and Method 2. Preparation of GO nanosheets 3

Asymmetric Organocatalytic Strecker-Type Reactions of Aliphatic N,N- Dialkylhydrazones

SUPPORTING INFORMATION. A simple asymmetric organocatalytic approach to optically active cyclohexenones

Effect of Conjugation and Aromaticity of 3,6 Di-substituted Carbazole On Triplet Energy

Supporting Information

Supplementary Materials for

Supporting Information. for

Red Color CPL Emission of Chiral 1,2-DACH-based Polymers via. Chiral Transfer of the Conjugated Chain Backbone Structure

Curtius-Like Rearrangement of Iron-Nitrenoid Complex and. Application in Biomimetic Synthesis of Bisindolylmethanes

Supporting Information

Organocatalytic enantioselective Michael addition of a kojic acid derivative to nitro olefins. Supporting Information

Supporting Information

The all-photochemical Synthesis an. OGP (10-14) Precursor

Structural Elucidation of Sumanene and Generation of its Benzylic Anions

An unusual dianion equivalent from acylsilanes for the synthesis of substituted β-keto esters

Supporting Information

Supporting Information

Supporting Information. Corporation, 1-1 Kurosakishiroishi, Yahatanishi-ku, Kitakyushu , Japan

Supporting Information

Synthesis of Levulinic Acid based Poly(amine-co-ester)s

Transcription:

Supporting Information N-Heterocyclic Carbene-Catalyzed Chemoselective Cross-Aza-Benzoin Reaction of Enals with Isatin-derived Ketimines: Access to Chiral Quaternary Aminooxindoles Jianfeng Xu 1, Chengli Mou 1,2, Tingshun Zhu 1, Bao-An Song 2 *, and Yonggui Robin Chi 1,2 * 1 Division of Chemistry & Biological Chemistry, School of Physical & Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore; 2 Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, Huaxi District, Guiyang 550025, China. robinchi@ntu.edu.sg Table of Contents I II III General information General procedure for the catalytic synthesis of products 3 X ray structure of product 3e References cited in the SI Characterization of products 1 H, 13 C NMR and HPLC spectra General Information Commercially available materials purchased from Alfa Aesar or Sigma-Aldrich were used as received. Proton nuclear magnetic resonance ( 1 H NMR) spectra were recorded on a Bruker BBFO (400 MHz) spectrometer. Chemical shifts were recorded in parts per million (ppm, δ) relative to tetramethylsilane (δ 0.00) or chloroform ( = 7.26, singlet). 1 H NMR splitting patterns are designated as s (singlet), d (doublet), t (triplet), q (quartet), dd (doublet of doublets); m (multiplet), and etc. All first-order splitting patterns were assigned on the basis of the appearance of the multiplet. Splitting patterns that could not be easily interpreted are designated as m (multiplet) or br (broad). Carbon nuclear magnetic resonance ( 13 C NMR) spectra were recorded on a Bruker BBFO (100 MHz) spectrometer. High resolution mass spectral analysis (HRMS) was performed on Finnigan MAT 95 XP mass spectrometer (Thermo Electron Corporation). The determination of er was performed via chiral HPLC analysis using Shimadzu LC-20AD HPLC workstation. X-ray crystallography analysis was performed on Bruker X8 APEX X-ray diffractionmeter. Optical rotations were measured using a 1 ml cell with a 1 dm path length on a Jasco P-1030 polarimeter and are reported as follows: [α] rt D (c in g per 100 ml solvent). Analytical thin-layer chromatography (TLC) was carried out on Merck 60 F254 pre-coated silica gel plate (0.2 mm thickness). Visualization was performed using a UV lamp. All substituted isatin-derived ketimines were synthesized according to literatures. 1

General procedure for the catalytic synthesis of products 3: A 10 ml dry Schlenk tube, equipped with a magnetic stir bar, was charged with chiral NHC catalyst F (0.01 mmol), KOAc (0.10 mmol) and 4 Å MS powder (100 mg). The tube was sealed with a septum, evacuated and refilled with nitrogen (3 cycles). CHCl 3 (1.0 ml), enal 1 (0.15 mmol), isatin-derived ketimine 2 (0.10 mmol) were then added successively and the reaction mixture was allowed to stir for 8 or 12 hours at room temperature. After completion of the reaction, the reaction mixture was concentrated under reduced pressure and the residue was subjected to column chromatography directly using hexane/etoac = 2/1 as eluent to afford the desired product 3. Note: The racemic catalyst that used for the preparation of the corresponding racemic products for HPLC analysis was synthesized by mixing the following two chiral NHC catalysts in a 1:1 ratio. Stereochemistry determination via X-ray crystallographic analysis: Absolute configurations of the products 3 were assigned based on the crystal X-ray structures of 3e. CCDC 978849 (3e, obtained as colorless needles via evaporation of a hexane/et 2 O solution) contains the supplementary X-ray crystallographic data. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif. References cited in the SI: 1. (a) Cali, P.; Begtrup, M. Synthesis 2002, 1, 63. (b) Yan, W.; Wang, D.; Feng, J.; Li, P.; Zhao, D.; Wang, R. Org. Lett. 2012, 14, 2512.

Characterization of products: (R,E)-tert-butyl (3-cinnamoyl-1-methyl-2-oxoindolin-3-yl)carbamate (3a): 28.2 mg, 72% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.81 (d, J = 15.2 Hz, 1H), 7.41-7.31 (m, 6H), 7.15 (d, J = 7.2 Hz, 1H), 7.09 (t, J = 7.6 Hz, 1H), 7.00 (d, J = 7.6 Hz, 1H), 6.72 (br, 1H), 6.21 (d, J = 15.6 Hz, 1H), 3.39 (s, 3H), 1.37 (s, 6H), 1.09 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.8, 171.9, 153.4, 147.0, 144.9, 133.7, 131.2, 130.3, 128.9, 128.6, 126.1, 123.7, 123.4, 117.7, 108.9, 80.4, 71.5, 28.2, 27.2; HRMS (ESI, m/z): calcd. for C 23 H 24 N 2 O 4 H + 393.1814, found 393.1818. [α] 21 D = -63.6 (c = 1.0 in CHCl 3 ); HPLC analysis: 97:3 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 27.9 min (major), 37.8 min (minor)]. (R,E)-tert-butyl (1-methyl-2-oxo-3-(3-(p-tolyl)acryloyl)indolin-3-yl)carbamate (3b): 30.9 mg, 76% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.79 (d, J = 15.6 Hz, 1H), 7.40 (t, J = 7.2 Hz, 1H), 7.22 (d, J = 8.0 Hz, 2H), 7.15-7.08 (m, 4H), 6.99 (d, J = 7.6 Hz, 1H), 6.73 (br, 1H), 6.16 (d, J = 15.2 Hz, 1H), 3.39 (s, 3H), 2.33 (s, 3H), 1.37 (s, 6H), 1.09 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.7, 172.0, 153.4, 147.1, 144.9, 142.0, 131.0, 130.2, 129.6, 128.7, 126.3, 123.6, 123.4, 116.6, 108.8, 80.3, 71.4, 28.2, 27.1, 21.5; HRMS (ESI, m/z): calcd. for C 24 H 26 N 2 O 4 H + 407.1971, found 407.1972. [α] 21 D = -48.6 (c = 1.0 in CHCl 3 ); HPLC analysis: 96:4 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 52.7 min (major), 75.3 min (minor)]. (R,E)-tert-butyl (3-(3-(4-methoxyphenyl)acryloyl)-1-methyl-2-oxoindolin-3-yl) carbamate (3c): 26.6 mg, 63% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.78 (d, J = 15.6 Hz, 1H), 7.40 (t, J = 7.6 Hz, 1H), 7.29 (d, J = 8.8 Hz, 2H), 7.14 (d, J = 7.2 Hz, 1H), 7.08 (t, J = 7.2 Hz, 1H), 6.99 (d, J = 7.6 Hz, 1H), 6.82 (d, J = 8.8 Hz, 2H), 6.75 (br, 1H), 6.07 (d, J = 15.6 Hz, 1H), 3.80 (s, 3H), 3.39 (s, 3H), 1.37 (s, 6H), 1.09 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.6, 172.1, 162.2, 153.4, 146.8, 144.7, 130.6, 130.1, 126.5, 123.6, 123.3, 115.1, 114.4, 108.8, 80.3, 71.3, 55.4, 28.2, 27.1; HRMS (ESI, m/z): calcd. for C 24 H 26 N 2 O 5 H + 423.1920, found 423.1925. [α] 21 D = -26.4 (c = 1.0 in CHCl 3 ); HPLC analysis: 97:3 er, [CHIRALPAK IC column; 0.9 ml/min; solvent

system: i-proh/hexane = 30:70; retention times: 40.1 min (major), 60.2 min (minor)]. (R,E)-tert-butyl (3-(3-(3-fluorophenyl)acryloyl)-1-methyl-2-oxoindolin-3-yl) carbamate (3d): 23.4 mg, 57% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.75 (d, J = 15.6 Hz, 1H), 7.42 (t, J = 7.2 Hz, 1H), 7.32-7.29 (m, 1H), 7.15-6.98 (m, 6H), 6.70 (br, 1H), 6.18 (d, J = 15.6 Hz, 1H), 3.40 (s, 3H), 1.38 (s, 6H), 1.10 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.6, 171.8, 162.8 (d, J C, F = 240 Hz), 153.3, 145.5, 144.8, 135.8 (d, J C, F = 8 Hz), 130.5, 130.4 (d, J C, F = 3 Hz), 124.9, 123.5 (d, J C, F = 27 Hz), 118.9, 118.1 (d, J C, F = 22 Hz), 114.5 (d, J C, F = 21 Hz), 109.0, 80.4, 71.5, 28.2, 27.2; HRMS (ESI, m/z): calcd. for C 23 H 24 N 2 O 4 FH + 411.1720, found 411.1731. [α] 21 D = -75.4 (c = 1.0 in CHCl 3 ); HPLC analysis: 98:2 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 25.8 min (major), 33.9 min (minor)]. BocHN O O N Me 3e Cl (R,E)-tert-butyl (3-(3-(4-chlorophenyl)acryloyl)-1-methyl-2-oxoindolin-3-yl) carbamate (3e): 31.1 mg, 73% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.75 (d, J = 15.6 Hz, 1H), 7.42 (t, J = 7.6 Hz, 1H), 7.29-7.24 (m, 4H), 7.15 (d, J = 7.2 Hz, 1H), 7.10 (t, J = 7.2 Hz, 1H), 7.00 (d, J = 7.6 Hz, 1H), 6.70 (br, 1H), 6.17 (d, J = 15.6 Hz, 1H), 3.40 (s, 3H), 1.37 (s, 6H), 1.09 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.7, 171.9, 153.4, 145.5, 144.9, 137.3, 132.2, 130.4, 129.8, 129.2, 125.9, 123.8, 123.5, 118.1, 108.9, 80.4, 71.5, 28.2, 27.3; HRMS (ESI, m/z): calcd. for C 23 H 23 N 2 O 4 ClH + 427.1425, found 427.1424. [α] 21 D = -32.8 (c = 1.0 in CHCl 3 ); HPLC analysis: 98:2 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 37.2 min (major), 54.0 min (minor)]. BocHN O O N Me 3f Br (R,E)-tert-butyl (3-(3-(4-bromophenyl)acryloyl)-1-methyl-2-oxoindolin-3-yl) carbamate (3f): 30.6 mg, 65% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.73 (d, J = 15.6 Hz, 1H), 7.46-7.40 (m, 3H), 7.19-7.10 (m, 4H), 7.01 (d, J = 8.0 Hz, 1H), 6.69 (br, 1H), 6.18 (d, J = 15.2 Hz, 1H), 3.39 (s, 3H), 1.37 (s, 6H), 1.09 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.6, 171.8, 153.3, 145.6, 144.8, 132.6, 132.2, 131.6, 130.4, 129.9, 125.7, 123.7, 123.5, 118.1, 108.9, 80.4, 71.5, 28.2, 27.2; HRMS (ESI, m/z): calcd. for C 23 H 23 N 2 O 81 4 BrH + 473.0899, found 473.0895. [α] 21 D = -59.7 (c = 1.0 in CHCl 3 );

HPLC analysis: 98:2 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 31.5 min (major), 45.6 min (minor)]. (R,E)-tert-butyl (3-(3-(furan-2-yl)acryloyl)-1-methyl-2-oxoindolin-3-yl) carbamate (3g): 19.9 mg, 52% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.53 (d, J = 15.2 Hz, 1H), 7.41-7.38 (m, 2H), 7.14-7.08 (m, 2H), 6.99 (d, J = 8.0 Hz, 1H), 6.73 (br, 1H), 6.64 (d, J = 3.2 Hz, 1H), 6.44-6.42 (m, 1H), 6.08 (d, J = 15.2 Hz, 1H), 3.39 (s, 3H), 1.37 (s, 6H), 1.08 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.6, 172.0, 153.3, 150.6, 145.7, 144.9, 132.4, 130.2, 126.1, 123.6, 123.3, 118.1, 115.0, 112.9, 108.9, 80.3, 71.3, 28.2, 27.1; HRMS (ESI, m/z): calcd. for C 21 H 22 N 2 O 5 H + 383.1607, found 383.1593. [α] 21 D = -39.6 (c = 1.0 in CHCl 3 ); HPLC analysis: 92:8 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 36.3 min (major), 46.7 min (minor)]. (R,E)-tert-butyl (1-methyl-2-oxo-3-(3-(thiophen-2-yl)acryloyl)indolin-3-yl) carbamate (3h): 21.1 mg, 53% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.49 (d, J = 15.2 Hz, 1H), 7.42-7.36 (m, 2H), 7.23 (d, J = 3.6 Hz, 1H), 7.15-7.07 (m, 2H), 7.02-6.98 (m, 2H), 6.71 (br, 1H), 5.98 (d, J = 15.2 Hz, 1H), 3.38 (s, 3H), 1.37 (s, 6H), 1.09 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.4, 171.9, 161.5, 153.3, 144.8, 139.2, 133.0, 130.2, 130.0, 128.5, 126.1, 123.7, 123.3, 116.4, 108.8, 80.3, 71.3, 28.2, 27.1; HRMS (ESI, m/z): calcd. for C 21 H 22 N 2 O 4 SH + 399.1379, found 399.1383. [α] 21 D = -38.5 (c = 1.0 in CHCl 3 ); HPLC analysis: 97:3 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 39.5 min (major), 50.3 min (minor)]. BocHN O Me O N Me 3i (R,E)-tert-butyl (3-(but-2-enoyl)-1-methyl-2-oxoindolin-3-yl)carbamate (3i): 15.8 mg, 48% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.40 (s, 1H), 7.18-7.10 (m, 3H), 6.96 (d, J = 6.8 Hz, 1H), 6.67 (br, 1H), 5.66 (d, J = 15.2 Hz, 1H), 3.37 (s, 3H), 1.76 (d, J = 6.4 Hz, 3H), 1.36 (s, 6H), 1.07 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.4, 172.0, 153.3, 148.3, 144.9, 130.1, 126.0, 123.5, 123.3, 123.0, 108.8, 80.3, 71.0, 28.2, 27.1, 18.5; HRMS (ESI, m/z): calcd. for C 18 H 22 N 2 O 4 H + 331.1658, found 331.1653. [α] 21 D = -98.3 (c = 1.0 in CHCl 3 ); HPLC analysis: 92:8 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 24.1 min (major),

36.6 min (minor)]. (R,E)-tert-butyl (3-(hex-2-enoyl)-1-methyl-2-oxoindolin-3-yl)carbamate (3j): 17.9 mg, 50% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.39 (t, J = 6.4 Hz, 1H), 7.15-7.08 (m, 3H), 6.95 (d, J = 7.2 Hz, 1H), 6.65 (br, 1H), 5.63 (d, J = 15.2 Hz, 1H), 3.35 (s, 3H), 2.05-2.02 (m, 2H), 1.38-1.31 (m, 8H), 1.07 (s, 3H), 0.80 (t, J = 7.6 Hz, 3H),; 13 C NMR (100 MHz, CDCl 3 ) δ 186.6, 171.9, 153.3, 152.8, 144.8, 130.1, 126.1, 123.5, 123.3, 121.5, 108.8, 80.3, 71.1, 34.6, 28.2, 27.1, 20.9, 13.4; HRMS (ESI, m/z): calcd. for C 20 H 26 N 2 O 4 H + 359.1971, found 359.1976. [α] 21 D = -73.5 (c = 1.0 in CHCl 3 ); HPLC analysis: 93:7 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 19.7 min (major), 24.0 min (minor)]. (R,E)-tert-butyl (1-allyl-3-cinnamoyl-2-oxoindolin-3-yl)carbamate (3k): 25.9 mg, 62% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.80 (d, J = 15.6 Hz, 1H), 7.37-7.31 (m, 6H), 7.16 (d, J = 7.2 Hz, 1H), 7.08 (t, J = 7.2 Hz, 1H), 7.00 (d, J = 7.6 Hz, 1H), 6.72 (br, 1H), 6.30 (d, J = 15.6 Hz, 1H), 6.01-5.94 (m, 1H), 5.49 (d, J = 17.2 Hz, 1H), 5.33 (d, J = 9.6 Hz, 1H), 4.63 (br, 1H), 4.38 (br, 1H), 1.38 (s, 6H), 1.10 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.7, 171.6, 153.3, 147.0, 144.0, 133.8, 131.2, 131.1, 130.1, 128.9, 128.6, 126.1, 123.6, 123.5, 118.7, 117.8, 109.7, 80.3, 71.5, 43.2, 28.2; HRMS (ESI, m/z): calcd. for C 25 H 26 N 2 O 4 H + 419.1971, found 419.1972. [α] 21 D = -69.8 (c = 1.0 in CHCl 3 ); HPLC analysis: 97:3 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 22.7 min (major), 32.6 min (minor)]. (R,E)-tert-butyl (1-benzyl-3-cinnamoyl-2-oxoindolin-3-yl)carbamate (3l): 27.2 mg, 58% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.78 (d, J = 15.6 Hz, 1H), 7.50-7.48 (m, 2H), 7.35-7.23 (m, 7H), 7.15-6.98 (m, 5H), 6.77 (br, 1H), 6.13 (d, J = 15.2 Hz, 1H), 5.39 (br, 1H), 4.73 (br, 1H), 1.40 (s, 6H), 1.11 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.6, 171.8, 153.4, 147.0, 144.0, 135.6, 133.5, 131.2, 130.1, 129.1, 128.8, 128.6, 128.0, 127.9, 126.1, 123.6, 123.5, 117.8, 109.7, 80.4, 71.5, 44.8, 28.2; HRMS (ESI, m/z): calcd. for C 29 H 28 N 2 O 4 H + 469.2127, found 469.2132. [α] 21 D = -49.3 (c = 1.0 in CHCl 3 ); HPLC analysis: 97:3 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 22.6 min (major), 37.6 min (minor)].

(R,E)-tert-butyl (3-cinnamoyl-2-oxo-1-phenylindolin-3-yl)carbamate (3m): 25.0 mg, 55% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.85 (d, J = 15.2 Hz, 1H), 7.56-7.12 (m, 13H), 6.95 (s, 1H), 6.78 (br, 1H), 6.50 (d, J = 15.6 Hz, 1H), 1.40 (s, 6H), 1.15 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.6, 171.4, 153.5, 147.1, 145.1, 134.5, 133.7, 131.3, 130.1, 129.8, 129.0, 128.6, 128.4, 126.7, 126.5, 124.1, 123.7, 117.8, 110.0, 80.4, 71.6, 28.2; HRMS (ESI, m/z): calcd. for C 28 H 26 N 2 O 4 H + 455.1971, found 455.1979. [α] 21 D = -136.5 (c = 1.0 in CHCl 3 ); HPLC analysis: 93:7 er, [CHIRALPAK IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 21.1 min (major), 31.9 min (minor)]. (R,E)-tert-butyl (3-cinnamoyl-1,5-dimethyl-2-oxoindolin-3-yl)carbamate (3n): 26.8 mg, 66% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.80 (d, J = 15.6 Hz, 1H), 7.36-7.31 (m, 5H), 7.19 (d, J = 7.6 Hz, 1H), 6.96 (s, 1H), 6.89 (d, J = 8.0 Hz, 1H), 6.71 (br, 1H), 6.22 (d, J = 15.6 Hz, 1H), 3.38 (s, 3H), 2.29 (s, 3H), 1.39 (s, 6H), 1.10 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.9, 171.8, 153.3, 146.8, 142.4, 133.7, 133.3, 131.2, 130.6, 128.9, 128.6, 125.9, 124.1, 117.7, 108.6, 80.3, 71.5, 28.2, 27.2, 21.0; HRMS (ESI, m/z): calcd. for C 24 H 26 N 2 O 4 H + 407.1971, found 407.1976. [α] 21 D = -7.2 (c = 1.0 in CHCl 3 ); HPLC analysis: 96:4 er, [CHIRALPAK IC column; 0.9 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 31.3 min (major), 48.8 min (minor)]. (R,E)-tert-butyl (3-cinnamoyl-5-methoxy-1-methyl-2-oxoindolin-3-yl)carbamate (3o): 30.0 mg, 71% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.81 (d, J = 15.6 Hz, 1H), 7.37-7.31 (m, 5H), 6.92 (s, 2H), 6.76 (s, 1H), 6.72 (br, 1H), 6.24 (d, J = 15.6 Hz, 1H), 3.75 (s, 3H), 3.37 (s, 3H), 1.39 (s, 6H), 1.12 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.7, 171.5, 156.7, 153.4, 147.0, 138.2, 133.7, 131.3, 128.9, 128.7, 127.2, 117.6, 114.5, 110.3, 109.4, 80.4, 71.8, 55.7, 28.2, 27.3; HRMS (ESI, m/z): calcd. for C 24 H 26 N 2 O 5 H + 423.1920, found 423.1914. [α] 21 D = -14.4 (c = 1.0 in CHCl 3 ); HPLC analysis: 97:3 er, [CHIRALCEL OD-H column; 0.5 ml/min; solvent system: i-proh/hexane = 5:95; retention times: 29.6 min (minor), 34.5 min (major)].

(R,E)-tert-butyl (3-cinnamoyl-1,7-dimethyl-2-oxoindolin-3-yl)carbamate (3p): 30.0 mg, 74% yield. 1 H NMR (400 MHz, CDCl 3 ) δ 7.80 (d, J = 15.6 Hz, 1H), 7.39-7.30 (m, 5H), 7.12 (s, 1H), 6.97 (s, 2H), 6.72 (br, 1H), 6.24 (d, J = 15.6 Hz, 1H), 3.65 (s, 3H), 2.67 (s, 3H), 1.38 (s, 6H), 1.13 (s, 3H); 13 C NMR (100 MHz, CDCl 3 ) δ 186.8, 172.7, 153.3, 147.0, 142.6, 134.1, 133.8, 131.2, 128.9, 128.7, 126.6, 123.6, 121.4, 120.4, 117.7, 80.2, 71.0, 30.6, 28.2, 19.1; HRMS (ESI, m/z): calcd. for C 24 H 26 N 2 O 4 H + 407.1971, found 407.1968. [α] 21 D = -95.9 (c = 1.0 in CHCl 3 ); HPLC analysis: 98:2 er, [CHIRALCEL IC column; 1.0 ml/min; solvent system: i-proh/hexane = 30:70; retention times: 35.3 min (major), 49.9 min (minor)].