POSS supported C2-symmetric bisprolinamide as a recyclable chiral catalyst for asymmetric Aldol reaction-Reference-Cited by-同舟云学术

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POSS supported C2-symmetric bisprolinamide as a recyclable chiral catalyst for asymmetric Aldol reaction

Published:2016-02 Issue: Volume:75 Page:23-27
ISSN:1566-7367
Container-title:Catalysis Communications
language:en
Short-container-title:Catalysis Communications

Author:

Zhou Yuan,Yang Guichun,Lu Cuifen,Nie Junqi,Chen Zuxing,Ren Jun

Funder

Science and Technology Support Project of Hubei Province

Youth Foundation of Hubei Province

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,General Chemistry,Catalysis

Reference24 articles.

1. Catalytic asymmetric aldol reactions in aqueous media

2. The direct catalytic asymmetric aldol reaction

3. A Liquid-Liquid Biphasic Homogeneous Organocatalytic Aldol Protocol Based on the Use of a Silica Gel Bound Multilayered Ionic Liquid Phase

4. Simple Ionic Liquid SupportedC2-Symmetric Bisprolinamides as Recoverable Organocatalysts for the Asymmetric Aldol Reaction in the Presence of Water

5. (1R,2R)-Bis[(S)-prolinamido]cyclohexane Modified with Ionic Groups: The First C2-Symmetric Immobilized Organocatalyst for Asymmetric Aldol Reactions in Aqueous Media

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3. Synthesis of Octachloro- and Octaazido-Functionalized T₈-Cages and Application to Recyclable Palladium Catalyst;Inorganic Chemistry;2022-01-07

4. A 2000 to 2020 Practitioner’s Guide to Chiral Amine Based Enantioselective Aldol Reactions:Common Ketone Substrates,Best Methods,in Water Reaction Environments,and Defining Nuances;European Journal of Organic Chemistry;2021-09

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