Diastereoselective Aziridination of 2-B(pin)-Substituted Allylic Alcohols: An Efficient Approach to Novel Organoboron Compounds-Reference-Cited by-同舟云学术

Diastereoselective Aziridination of 2-B(pin)-Substituted Allylic Alcohols: An Efficient Approach to Novel Organoboron Compounds

Published:2011-10-25 Issue:22 Volume:13 Page:6094-6097
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hernández-Toribio Jorge¹,Hussain Mahmud M.¹,Cheng Kevin¹,Carroll Patrick J.¹,Walsh Patrick J.¹

Affiliation:

1. P. Roy and Diana T. Vagelos Laboratories, University of Pennsylvania, Department of Chemistry, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol202588g

Reference41 articles.

1. Expanding the scope of transformations of organoboron species: carbon–carbon bond formation with retention of configuration

2. Boronic acid compounds as potential pharmaceutical agents

3. Expanding Roles for Organoboron Compounds – Versatile and Valuable Molecules for Synthetic, Biological and Medicinal Chemistry

4. Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis

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