Total Synthesis of (+)-Aquaticol by Biomimetic Phenol Dearomatization: Double Diastereofacial Differentiation in the Diels–Alder Dimerization of Orthoquinols with aC2-Symmetric Transition State-Reference-Cited by-同舟云学术

Total Synthesis of (+)-Aquaticol by Biomimetic Phenol Dearomatization: Double Diastereofacial Differentiation in the Diels–Alder Dimerization of Orthoquinols with aC2-Symmetric Transition State

Published:2007-02-19 Issue:9 Volume:119 Page:1555-1557
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

Gagnepain Julien,Castet Frédéric,Quideau Stéphane

Publisher

Wiley

Subject

General Medicine

Reference24 articles.

1. Aquaticol, a novel bis-sesquiterpene from Veronica anagallis-aquatica

2. For a recent review on the chemistry of orthoquinols and related species, see: in Modern Arene Chemistry (Ed.: ), Wiley-VCH, Weinheim, 2002, pp. 539–573.

3. (S)-2-hydroxycuparene [p-(1,2,2-trimethylcyclopentyl)-o-cresol] and 3,4′-ethylenebisphenol from a liverwort, Marchantia polymorpha linn

4. An unusual dimeric sesquiterpene and other constituents from Chilean Baccharis species

5. Dehydration of dimeric 6-hydroxycyclohexa-2,4-dienones–an alternative course for these reactions and a model for the maytenone to anhydromaytenone transformation

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