Facile access to functionalized chiral secondary benzylic boronic esters via catalytic asymmetric hydroboration-Reference-Cited by-同舟云学术

Facile access to functionalized chiral secondary benzylic boronic esters via catalytic asymmetric hydroboration

Published:2019 Issue:18 Volume:10 Page:4854-4861
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Chakrabarty Suman¹²³⁴^ORCID,Palencia Hector¹⁵⁶⁴^ORCID,Morton Martha D.¹²³⁴⁷^ORCID,Carr Ryan O.¹²³⁴^ORCID,Takacs James M.¹²³⁴⁷^ORCID

Affiliation:

1. Department of Chemistry

2. University of Nebraska-Lincoln

3. Lincoln

4. USA

5. University of Nebraska-Kearney

6. Kearney

7. Nebraska Center for Integrated Biomolecular Communication (NCIBC)

Abstract

Allylic and homoallylic phosphonates undergo asymmetric hydroboration yielding chiral boronic esters (yields up to 86%, enantiomer ratios up to 99 : 1).

Funder

National Institute of General Medical Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/SC/C8SC05613G

Reference71 articles.

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