Microwave-assisted Diels–Alder reaction of 1,3,3-trimethyl-2-vinyl-1-cyclohexene with chromones — An expeditious approach to analogues of the puupehenone group of marine diterpenoids and kampanols-Reference-Cited by-同舟云学术

Microwave-assisted Diels–Alder reaction of 1,3,3-trimethyl-2-vinyl-1-cyclohexene with chromones — An expeditious approach to analogues of the puupehenone group of marine diterpenoids and kampanols

Published:2010-12 Issue:12 Volume:88 Page:1233-1239
ISSN:0008-4042
Container-title:Canadian Journal of Chemistry
language:en
Short-container-title:Can. J. Chem.

Author:

Kamble Rajesh M.¹,Ramana M. M.V.¹

Affiliation:

1. Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400 098, India.

Abstract

A rapid assembly of the tetracyclic core of marine diterpenoids related to puupehenone and kampanols by a Diels–Alder reaction of 1,3,3-trimethyl-2-vinyl-1-cyclohexene with chromones under microwave irradiation with or without TiCl4 is described.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Link

http://www.nrcresearchpress.com/doi/pdf/10.1139/V10-137

Reference48 articles.

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3. The stereospecific synthesis of D,L-Winterin

4. The Diels–Alder route to drimane related sesquiterpenes; synthesis of cinnamolide, polygodial, isodrimeninol, drimenin and warburganal

5. Regioselective preparation of tricyclic terpene ring systems by cycloaddition of 1,3,3-trimethyl-2-vinylcyclohexene with unsymmetrical quinones

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