Experimental and theoretical evaluation of trans-3-halo-2-hydroxy-tetrahydropyran conformational preferences. Beyond anomeric interaction-Reference-Cited by-同舟云学术

Experimental and theoretical evaluation of trans-3-halo-2-hydroxy-tetrahydropyran conformational preferences. Beyond anomeric interaction

Published:2015 Issue:45 Volume:5 Page:35412-35420
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Barbosa Thaís M.¹²³⁴,Viesser Renan V.¹²³⁴,Abraham Raymond J.⁵⁶⁷⁸,Rittner Roberto¹²³⁴,Tormena Cláudio F.¹²³⁴

Affiliation:

1. Chemistry Institute

2. University of Campinas – UNICAMP

3. Campinas

4. Brazil

5. Department of Chemistry

6. University of Liverpool

7. Liverpool

8. UK

Abstract

Which analysis will explain the preferences of the substituents in the hydro-halo-tetrahydropyran rings? Is the anomeric effect essential to understand what is going on?

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA04968G

Reference29 articles.

1. The Role of Hyperconjugation in the Conformational Analysis of Methylcyclohexane and Methylheterocyclohexanes

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4. Stereoelectronic Interaction and Their Effects on Conformational Preference for 2-Substituted Methylenecyclohexane: An Experimental and Theoretical Investigation

5. Interaction in trans-2-halocyclohexanols — an infrared and theoretical study

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