Functionalized Chiral Ionic Liquid Catalyzed Enantioselective Desymmetrizations of Prochiral Ketones via Asymmetric Michael Addition Reaction

Sanzhong Luo; Long Zhang; Xueling Mi; Yupu Qiao; Jin-Pei Cheng

doi:10.1021/jo7020357

Functionalized Chiral Ionic Liquid Catalyzed Enantioselective Desymmetrizations of Prochiral Ketones via Asymmetric Michael Addition Reaction

The Journal of Organic Chemistry ◽

10.1021/jo7020357 ◽

2007 ◽

Vol 72 (24) ◽

pp. 9350-9352 ◽

Cited By ~ 90

Author(s):

Sanzhong Luo ◽

Long Zhang ◽

Xueling Mi ◽

Yupu Qiao ◽

Jin-Pei Cheng

Keyword(s):

Ionic Liquid ◽

Michael Addition ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Asymmetric Michael Addition ◽

Chiral Ionic Liquid ◽

Prochiral Ketones

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ChemInform Abstract: Functionalized Chiral Ionic Liquid Catalyzed Enantioselective Desymmetrizations of Prochiral Ketones via Asymmetric Michael Addition Reaction.

ChemInform ◽

10.1002/chin.200813060 ◽

2008 ◽

Vol 39 (13) ◽

Author(s):

Sanzhong Luo ◽

Long Zhang ◽

Xueling Mi ◽

Yupu Qiao ◽

Jin-Pei Cheng

Keyword(s):

Ionic Liquid ◽

Michael Addition ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Asymmetric Michael Addition ◽

Chiral Ionic Liquid ◽

Prochiral Ketones

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A development of a reusable copper supported imidazolium functionalized ionic liquid catalyzed asymmetric Michael addition reaction

Journal of the Indian Chemical Society ◽

10.1016/j.jics.2021.100267 ◽

2021 ◽

pp. 100267

Author(s):

Bharathi Priya Velumani ◽

Subramani Ramya ◽

Uthayanila Selvarasu ◽

Parasuraman Karthikeyan

Keyword(s):

Ionic Liquid ◽

Michael Addition ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Functionalized Ionic Liquid ◽

Asymmetric Michael Addition

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The role of neutral anions in ionic liquid as solvent media for the reactivity and stereoselectivity towards asymmetric Michael addition reaction of n-pentanal with β-nitrostyrene catalyzed by L-Proline

Synthetic Communications ◽

10.1080/00397911.2019.1604969 ◽

2019 ◽

Vol 49 (12) ◽

pp. 1578-1591 ◽

Cited By ~ 1

Author(s):

Emmy M. Omar ◽

Mohd Basyaruddin A. Rahman ◽

Bukuo Ni ◽

Allan D. Headley

Keyword(s):

Ionic Liquid ◽

Michael Addition ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Asymmetric Michael Addition

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Polymerization Amplified Stereoselectivity (PASS) of Asymmetric Michael Addition Reaction and Aldol Reaction Catalyzed by Helical Poly(phenyl isocyanide) Bearing Secondary Amine Pendants

Macromolecules ◽

10.1021/acs.macromol.8b02088 ◽

2018 ◽

Vol 51 (23) ◽

pp. 9547-9554 ◽

Cited By ~ 13

Author(s):

Ling Shen ◽

Lei Xu ◽

Xiao-Hua Hou ◽

Na Liu ◽

Zong-Quan Wu

Keyword(s):

Secondary Amine ◽

Michael Addition ◽

Addition Reaction ◽

Aldol Reaction ◽

Michael Addition Reaction ◽

Asymmetric Michael Addition

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Knoevenagel condensation versus Michael addition reaction in ionic-liquid-catalyzed synthesis of hexahydroquinoline: a SMD–DFT study

Theoretical Chemistry Accounts ◽

10.1007/s00214-020-2565-4 ◽

2020 ◽

Vol 139 (3) ◽

Cited By ~ 2

Author(s):

R. Behjatmanesh-Ardakani ◽

N. Safaeian ◽

M. Oftadeh ◽

M. Fallah-Mehrjardi

Keyword(s):

Ionic Liquid ◽

Michael Addition ◽

Addition Reaction ◽

Knoevenagel Condensation ◽

Dft Study ◽

Michael Addition Reaction

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The design of a spiro-pyrrolidine organocatalyst and its application to catalytic asymmetric Michael addition for the construction of all-carbon quaternary centers

Chemical Communications ◽

10.1039/c5cc02765a ◽

2015 ◽

Vol 51 (49) ◽

pp. 9979-9982 ◽

Cited By ~ 21

Author(s):

Jin-Miao Tian ◽

Yong-Hai Yuan ◽

Yong-Qiang Tu ◽

Fu-Min Zhang ◽

Xiao-Bo Zhang ◽

...

Keyword(s):

Michael Addition ◽

Addition Reaction ◽

Silyl Ether ◽

Michael Addition Reaction ◽

Quaternary Centers ◽

Asymmetric Michael Addition ◽

Catalytic Asymmetric

A novel chiral spiro-pyrrolidine silyl ether organocatalyst has been designed and applied to an asymmetric Michael addition reaction.

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ChemInform Abstract: An Alternative Synthesis of Chiral (S)-Proline Derivatives that Contain a Thiohydantoin Moiety and Their Application as Organocatalysts in the Asymmetric Michael Addition Reaction under Solvent-Free Conditions.

ChemInform ◽

10.1002/chin.201444022 ◽

2014 ◽

Vol 45 (44) ◽

pp. no-no

Author(s):

Alberto Vega-Penaloza ◽

Omar Sanchez-Antonio ◽

C. Gabriela Avila-Ortiz ◽

Margarita Escudero-Casao ◽

Eusebio Juaristi

Keyword(s):

Michael Addition ◽

Addition Reaction ◽

Solvent Free ◽

Michael Addition Reaction ◽

Alternative Synthesis ◽

Asymmetric Michael Addition ◽

Solvent Free Conditions ◽

Proline Derivatives

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Optimization of Microwave-Assisted Michael Addition Reaction Catalyzed by L-Proline in Ionic Liquid Medium Using Response Surface Methodology

Synthetic Communications ◽

10.1080/00397911.2013.808348 ◽

2013 ◽

Vol 44 (3) ◽

pp. 381-398 ◽

Cited By ~ 5

Author(s):

Emmy M. Omar ◽

Mohd Basyaruddin A. Rahman ◽

Emilia Abdulmalek ◽

Bimo A. Tejo ◽

Bukuo Ni ◽

...

Keyword(s):

Response Surface Methodology ◽

Ionic Liquid ◽

Liquid Medium ◽

Response Surface ◽

Michael Addition ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Microwave Assisted ◽

Ionic Liquid Medium

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ChemInform Abstract: Optimization of Microwave-Assisted Michael Addition Reaction Catalyzed by L-Proline in Ionic Liquid Medium Using Response Surface Methodology.

ChemInform ◽

10.1002/chin.201423025 ◽

2014 ◽

Vol 45 (23) ◽

pp. no-no

Author(s):

Emmy M. Omar ◽

Mohd Basyaruddin A. Rahman ◽

Emilia Abdulmalek ◽

Bimo A. Tejo ◽

Bukuo Ni ◽

...

Keyword(s):

Response Surface Methodology ◽

Ionic Liquid ◽

Liquid Medium ◽

Response Surface ◽

Michael Addition ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Microwave Assisted ◽

Abstract Optimization ◽

Ionic Liquid Medium

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A new methodology for the stereoselective synthesis of 4-substituted butenolides: Asymmetric Michael addition reaction of 2-(trimethylsilyloxy)furans to oxazolidinone enoates

Tetrahedron ◽

10.1016/s0040-4020(97)10152-1 ◽

1997 ◽

Vol 53 (50) ◽

pp. 17015-17028 ◽

Cited By ~ 87

Author(s):

Hiroshi Kitajima ◽

Katsuji Ito ◽

Tsutomu Katsuki

Keyword(s):

Michael Addition ◽

Stereoselective Synthesis ◽

Addition Reaction ◽

Michael Addition Reaction ◽

Asymmetric Michael Addition

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