Efficient Access to Orthoquinols and Their [4 + 2] Cyclodimers via SIBX-Mediated Hydroxylative Phenol Dearomatization-Reference-Cited by-同舟云学术

Efficient Access to Orthoquinols and Their [4 + 2] Cyclodimers via SIBX-Mediated Hydroxylative Phenol Dearomatization

Published:2007-07-12 Issue:16 Volume:72 Page:6280-6283
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lebrasseur Nathalie¹,Gagnepain Julien¹,Ozanne-Beaudenon Aurélie¹,Léger Jean-Michel¹,Quideau Stéphane¹

Affiliation:

1. Université de Bordeaux, Institut Européen de Chimie et Biologie, 2 rue Robert Escarpit, 33607 Pessac Cedex, France, Institut des Sciences Moléculaires (CNRS-UMR 5255), 351 cours de la Libération, 33405 Talence Cedex, France, and Laboratoire de Pharmacochimie, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France s.quideau@iecb.u-bordeaux.fr

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0708893

Reference34 articles.

1. SYNTHETIC USES OF ORTHOQUINONE MONOKETALS AND THEIR ORTHOQUINOL VARIANTS. A REVIEW

2. Cyclohexadienone Ketals and Quinols: Four Building Blocks Potentially Useful for Enantioselective Synthesis

3. Biosynthesis of bitter acids in hops. A 13C-NMR and 2H-NMR study on the building blocks of humulone

4. The Chemistry of Hop Constituents

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