Enantioselective Reduction of Prochiral Ketones with NaBH4/Me2SO4/(S)-Me-CBS-Reference-Cited by-同舟云学术

Enantioselective Reduction of Prochiral Ketones with NaBH4/Me2SO4/(S)-Me-CBS

Published:2014-04-29 Issue:10 Volume:44 Page:1515-1520
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Zhou Yuhan¹,Gao Guchao¹,Song Yuming¹,Qu Jingping¹

Affiliation:

1. a State Key Laboratory of Fine Chemicals , School of Pharmaceutical Science and Technology, Dalian University of Technology , Dalian , China

Funder

We are grateful to the National Natural Science Foundation of China (No. 20676019), the Fundamental Research Funds for the Central Universities (No. DUT13LAB03), and the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry for financial support of this work. We also thank Baomin Wang for valuable discussions.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2013.862834

Reference20 articles.

1. Boron Reagents in Process Chemistry: Excellent Tools for Selective Reductions

2. Regioselectivity of the Rhodium-Catalyzed Hydroboration of Vinyl Arenes: Electronic Twists and Mechanistic Shifts

3. Structurally Well-Defined, Recoverable C3-Symmetric Tris(β-hydroxy phosphoramide)-Catalyzed Enantioselective Borane Reduction of Ketones

4. Asymmetric Reduction of Oxime Ethers Promoted by Chiral Spiroborate Esters with an O3BN Framework

5. Synthesis and properties of a neutral derivative of diethylenetriaminepentaacetic acid (DTPA)

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