The control of stereochemistry by the pentafluorosulfanyl group-Reference-Cited by-同舟云学术

The control of stereochemistry by the pentafluorosulfanyl group

Published:2018 Issue:17 Volume:16 Page:3151-3159
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Savoie Paul R.¹²³⁴⁵,von Hahmann Cortney N.¹²³⁴⁵,Penger Alexander¹²³⁴⁵,Wei Zheng¹²³⁴⁵,Welch John T.¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. University at Albany

3. SUNY

4. Albany

5. USA

Abstract

The steric and electron withdrawing effects of the pentafluorosulfanyl group effectively direct the diastereoselectivity of the Staudinger reaction.

Funder

Directorate for Mathematical and Physical Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C7OB03146G

Reference77 articles.

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2. R. W. Winter , R. A.Dodean , G. L.Gard and V. A.Soloshonok , in Fluorine Containing Synthons , ed. V. A. Soloshonok , American Chemical Society , Washington D.C. , 2005 , vol. 911 , pp. 87–118

3. Synthetic chemistry and biological activity of pentafluorosulphanyl (SF5) organic molecules

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