Stereoselective Formation of Trisubstituted Vinyl Boronate Esters by the Acid-Mediated Elimination of α-Hydroxyboronate Esters-Reference-Cited by-同舟云学术

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Stereoselective Formation of Trisubstituted Vinyl Boronate Esters by the Acid-Mediated Elimination of α-Hydroxyboronate Esters

Published:2014-07-14 Issue:15 Volume:79 Page:7199-7204
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Guan Weiye¹²,Michael Alicia K.¹²,McIntosh Melissa L.¹²,Koren-Selfridge Liza¹²,Scott John P.¹²,Clark Timothy B.¹²

Affiliation:

1. Department of Chemistry and Biochemistry, University of San Diego, 5998 Alcala Park, San Diego, California 92110, United States

2. Department of Chemistry, Western Washington University, 516 High Street, Bellingham, Washington 98225, United States

Funder

National Institutes of Health

Research Corporation for Science Advancement

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo500773t

Reference31 articles.

1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

2. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998

3. Hydroborations catalysed by transition metal complexes

4. Rhodium- or Iridium-Catalyzed trans-Hydroboration of Terminal Alkynes, Giving (Z)-1-Alkenylboron Compounds

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