Dimethyl sulfide facilitates acid catalysed ring opening of the bicyclic monoterpenes in crude sulfate turpentine to afford p-menthadienes in good yield-Reference-Cited by-同舟云学术

Dimethyl sulfide facilitates acid catalysed ring opening of the bicyclic monoterpenes in crude sulfate turpentine to afford p-menthadienes in good yield

Published:2021 Issue:1 Volume:23 Page:597-610
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Tibbetts Joshua D.¹²³⁴⁵^ORCID,Bull Steven D.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Bath

3. Bath

4. UK

5. Centre for Sustainable Chemical Technologies

Abstract

Dimethyl sulfide enables efficient acid-catalysed ring opening of bicyclic monoterpenes in turpentine to give p-menthadienes in up to 90% yields.

Funder

Engineering and Physical Sciences Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/GC/D0GC03452E

Reference64 articles.

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5. Renewable chemical feedstock supply network design: The case of terpenes

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