Highly Enantioselective Intramolecular Morita-Baylis-Hillman Reaction Catalyzed by Mannose-Based Thiourea-phosphine-Reference-Cited by-同舟云学术

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Highly Enantioselective Intramolecular Morita-Baylis-Hillman Reaction Catalyzed by Mannose-Based Thiourea-phosphine

Published:2015-09-29 Issue:10 Volume:33 Page:1111-1114
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Yang Weihong,Yuan Kui,Song Hongliang,Sha Feng,Wu Xinyan

Funder

National Natural Science Foundation of China

the Program for New Century Excellent Talents in University

the Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cjoc.201500468/fullpdf

Reference69 articles.

1. Deracemization of Baylis−Hillman Adducts

2. An enantio- and stereocontrolled synthesis of (–)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis–Hillman reaction

3. DYKAT of Baylis−Hillman Adducts: Concise Total Synthesis of Furaquinocin E

4. A Highly Chemoselective, Diastereoselective, and Regioselective Epoxidation of Chiral Allylic Alcohols with Hydrogen Peroxide, Catalyzed by Sandwich-Type Polyoxometalates: Enhancement of Reactivity and Control of Selectivity by the Hydroxy Group through Metal−Alcoholate Bonding

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2. The Application of Biocatalysis in the Preparation and Resolution of Morita‐Baylis‐Hillman Adducts and Their Derivatives;ChemBioChem;2021-12-06

3. Asymmetric Reactions Catalyzed by Chiral Tertiary Phosphines;Chinese Journal of Chemistry;2020-08-27

4. Valorization of Waste: Sustainable Organocatalysts from Renewable Resources;ChemSusChem;2019-11-22

5. Reactions of Aldehydes and Ketones and Their Derivatives;Organic Reaction Mechanisms Series;2019-03-07

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