Highly Enantio- and Diastereoselective l-Proline Derived Acetylglucose Amide Catalyzed Aldol Reaction of Ketones to Aldehydes under Solvent-Free Conditions-Reference-Cited by-同舟云学术

Highly Enantio- and Diastereoselective l-Proline Derived Acetylglucose Amide Catalyzed Aldol Reaction of Ketones to Aldehydes under Solvent-Free Conditions

Published:2015-10-21 Issue:20 Volume:26 Page:2858-2862
ISSN:0936-5214
Container-title:Synlett
language:en
Short-container-title:Synlett

Author:

Han Xiaoyu¹,Zeng Xiaofei²,Wang Yongjiang¹,Gai Xikun¹

Affiliation:

1. Zhejiang Provincial Key Laboratory for Chemical &Biological Processing Technology of Farm Products, School of Biological and Chemical Engineering, Zhejiang University of Science and Technology

2. College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1560701.pdf

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2. Organocatalytic asymmetric aldol reaction using protonated chiral 1,2-diamines;Tetrahedron Letters;2020-09

3. A Simple and Efficient Protocol for Proline-Catalysed Asymmetric Aldol Reaction;Catalysts;2020-06-10

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5. Direct Asymmetric Mannich Reaction Catalyzed by a d-Glucosamine-Derived Organocatalyst;Synlett;2018-01-02