Asymmetric Allylboration of Aldehydes and Ketones Using 3,3‘-Disubstitutedbinaphthol-Modified Boronates-Reference-Cited by-同舟云学术

Asymmetric Allylboration of Aldehydes and Ketones Using 3,3‘-Disubstitutedbinaphthol-Modified Boronates

Published:2004-07-16 Issue:16 Volume:6 Page:2701-2704
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wu T. Robert¹,Shen Lixin¹,Chong J. Michael¹

Affiliation:

1. Guelph-Waterloo Centre for Graduate Work in Chemistry and Biochemistry, (GWC)2, Department of Chemistry, University of Waterloo, Waterloo, Ontario, Canada N2L 3G1

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0490882

Reference37 articles.

1. Highly enantioselective reduction of alkynyl ketones by a binaphthol-modified aluminum hydride reagent. Asymmetric synthesis of some insect pheromones

2. Insight into the Mechanism of the Asymmetric Addition of Alkyl Groups to Aldehydes Catalyzed by Titanium−BINOLate Species

3. Reactions of allylsilanes with simple iminium salts in water: A facile route to piperidines via a aminomethano desilylation-cyclization process

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