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Refinado por: Base de dados/Biblioteca: Science Citation Index Expanded (Web of Science) remover
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Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo‐ and Enantioconvergent Michael–Henry Reactions to Afford Spirooxindoles Bearing Furan‐Fused Rings
Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo‐ and Enantioconvergent Michael–Henry Reactions to Afford Spirooxindoles Bearing Furan‐Fused Rings
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Dynamic Kinetic Asymmetric Transformation of Racemic Diastereomers: Diastereo‐ and Enantioconvergent Michael–Henry Reactions to Afford Spirooxindoles Bearing Furan‐Fused Rings

Sohail, Muhammad ; Tanaka, Fujie

Angewandte Chemie (International ed.), 2021-09, Vol.60 (39), p.21256-21260 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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2
Organocatalytic Asymmetric Synthesis of Spiro‐Tetrahydrothiophene Oxindoles Bearing Four Contiguous Stereocenters by One‐Pot Michael–Henry‐Cascade–Rearrangement Reactions
Organocatalytic Asymmetric Synthesis of Spiro‐Tetrahydrothiophene Oxindoles Bearing Four Contiguous Stereocenters by One‐Pot Michael–Henry‐Cascade–Rearrangement Reactions
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Organocatalytic Asymmetric Synthesis of Spiro‐Tetrahydrothiophene Oxindoles Bearing Four Contiguous Stereocenters by One‐Pot Michael–Henry‐Cascade–Rearrangement Reactions

Wang, Shengzheng ; Guo, Zhongjie ; Chen, Shuqiang ; Jiang, Yan ; Zhang, Fan ; Liu, Xueying ; Chen, Weiping ; Sheng, Chunquan

Chemistry : a European journal, 2018-01, Vol.24 (1), p.62-66 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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3
Assembly of Spirooxindole Derivatives Containing Four Consecutive Stereocenters via Organocatalytic Michael–Henry Cascade Reactions
Assembly of Spirooxindole Derivatives Containing Four Consecutive Stereocenters via Organocatalytic Michael–Henry Cascade Reactions
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Assembly of Spirooxindole Derivatives Containing Four Consecutive Stereocenters via Organocatalytic Michael–Henry Cascade Reactions

Albertshofer, Klaus ; Tan, Bin ; Barbas, Carlos F

Organic letters, 2012-04, Vol.14 (7), p.1834-1837 [Periódico revisado por pares]

United States: American Chemical Society

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4
A New Henry/Michael/Retro-Henry/Henry Domino Sequence Promoted by Bifunctional Organocatalysts
A New Henry/Michael/Retro-Henry/Henry Domino Sequence Promoted by Bifunctional Organocatalysts
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A New Henry/Michael/Retro-Henry/Henry Domino Sequence Promoted by Bifunctional Organocatalysts

Quintavalla, Arianna ; Lombardo, Marco ; Sanap, Shrihari P. ; Trombini, Claudio

Advanced synthesis & catalysis, 2013-03, Vol.355 (5), p.938-946 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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5
Microwave assisted L‐proline catalyzed one‐pot three–component reaction for the synthesis of 4‐aminoaryl‐2‐phenyl‐2H‐3‐nitrochromene hybrid via Domino Michael‐Henry‐Michael addition reaction
Microwave assisted L‐proline catalyzed one‐pot three–component reaction for the synthesis of 4‐aminoaryl‐2‐phenyl‐2H‐3‐nitrochromene hybrid via Domino Michael‐Henry‐Michael addition reaction
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Microwave assisted L‐proline catalyzed one‐pot three–component reaction for the synthesis of 4‐aminoaryl‐2‐phenyl‐2H‐3‐nitrochromene hybrid via Domino Michael‐Henry‐Michael addition reaction

Khan, Danish ; Sharma, Saurabh ; Shukla, Prakhar

Journal of heterocyclic chemistry, 2022-06, Vol.59 (6), p.1064-1072 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Inc

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6
Diastereoselective Synthesis of Bicyclo[3.2.1]octanes via Catalyst‐Free Cascade Michael/Henry Reaction with a Functionalized Vinylogous Nucleophile
Diastereoselective Synthesis of Bicyclo[3.2.1]octanes via Catalyst‐Free Cascade Michael/Henry Reaction with a Functionalized Vinylogous Nucleophile
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Diastereoselective Synthesis of Bicyclo[3.2.1]octanes via Catalyst‐Free Cascade Michael/Henry Reaction with a Functionalized Vinylogous Nucleophile

An, Laiyu ; Chen, Linghong ; Yang, Hongzhou ; Ye, Ling ; Yang, Hongjun ; Li, Xinying ; Zhao, Zhigang ; Li, Xuefeng

Advanced synthesis & catalysis, 2023-09, Vol.365 (17), p.2969-2975 [Periódico revisado por pares]

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7
Formal (4+1) Cycloaddition and Enantioselective Michael–Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles
Formal (4+1) Cycloaddition and Enantioselective Michael–Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles
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Formal (4+1) Cycloaddition and Enantioselective Michael–Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles

Huang, Ji‐Rong ; Sohail, Muhammad ; Taniguchi, Tohru ; Monde, Kenji ; Tanaka, Fujie

Angewandte Chemie (International ed.), 2017-05, Vol.56 (21), p.5853-5857 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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8
Synthesis of Optically Active 2H-Thiopyrano[2,3-b]quinolines with Three Contiguous Stereocenters via an Organocatalytic Asymmetric Tandem Michael-Henry Reaction
Synthesis of Optically Active 2H-Thiopyrano[2,3-b]quinolines with Three Contiguous Stereocenters via an Organocatalytic Asymmetric Tandem Michael-Henry Reaction
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Synthesis of Optically Active 2H-Thiopyrano[2,3-b]quinolines with Three Contiguous Stereocenters via an Organocatalytic Asymmetric Tandem Michael-Henry Reaction

Wu, Lulu ; Wang, Youming ; Song, Haibin ; Tang, Liangfu ; Zhou, Zhenghong ; Tang, Chuchi

Advanced synthesis & catalysis, 2013-04, Vol.355 (6), p.1053-1057 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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9
Double Diastereocontrol in Bifunctional Thiourea Organocatalysis: Iterative Michael–Michael–Henry Sequence Regulated by the Configuration of Chiral Catalysts
Double Diastereocontrol in Bifunctional Thiourea Organocatalysis: Iterative Michael–Michael–Henry Sequence Regulated by the Configuration of Chiral Catalysts
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Double Diastereocontrol in Bifunctional Thiourea Organocatalysis: Iterative Michael–Michael–Henry Sequence Regulated by the Configuration of Chiral Catalysts

Varga, Szilárd ; Jakab, Gergely ; Drahos, László ; Holczbauer, Tamás ; Czugler, Mátyás ; Soós, Tibor

Organic letters, 2011-10, Vol.13 (20), p.5416-5419 [Periódico revisado por pares]

United States: American Chemical Society

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10
Asymmetric Organocatalytic Michael/Henry Domino Reactions through Hydrogen-Bond Activation: Kinetic Access to Indane Scaffolds Bearing cis-Vicinal Substituents
Asymmetric Organocatalytic Michael/Henry Domino Reactions through Hydrogen-Bond Activation: Kinetic Access to Indane Scaffolds Bearing cis-Vicinal Substituents
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Asymmetric Organocatalytic Michael/Henry Domino Reactions through Hydrogen-Bond Activation: Kinetic Access to Indane Scaffolds Bearing cis-Vicinal Substituents

Loh, Charles C. J. ; Atodiresei, Iuliana ; Enders, Dieter

Chemistry : a European journal, 2013-08, Vol.19 (33), p.10822-10826 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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