The stereodivergent formation of 2,6-cis and 2,6-trans-tetrahydropyrans: experimental and computational investigation of the mechanism of a thioester oxy-Michael cyclization-Reference-Cited by-同舟云学术

The stereodivergent formation of 2,6-cis and 2,6-trans-tetrahydropyrans: experimental and computational investigation of the mechanism of a thioester oxy-Michael cyclization

Published:2017 Issue:1 Volume:8 Page:482-490
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Ermanis Kristaps¹²³⁴^ORCID,Hsiao Yin-Ting¹²³⁴,Kaya Uğur¹²³⁴,Jeuken Alan¹²³⁴,Clarke Paul A.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of York

3. York

4. UK

Abstract

Computational and synthetic studies have elucidated the origins of stereodivergence in an oxy-Michael synthesis of 2,6-disubstituted tetrahydropyrans.

Funder

University of York

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/SC/C6SC03478K

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