Diterpene Chemistry. XI. Synthesis of Perfumery Compounds from Labda-8(17),14-dien-13-ol (Manool)-Reference-Cited by-同舟云学术

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Diterpene Chemistry. XI. Synthesis of Perfumery Compounds from Labda-8(17),14-dien-13-ol (Manool)

Published:1979 Issue:6 Volume:32 Page:1395
ISSN:0004-9425
Container-title:Australian Journal of Chemistry
language:en
Short-container-title:Aust. J. Chem.

Author:

Grant PK,Rowan DD

Abstract

The potentially odiferous isomeric acetals 8,13:8,14-diepoxy-15,16,17-trinorlabdanes have been synthesized from manool. A Tanabe-Eschenmoser fragmentation provided the crucial intermediate.

Publisher

CSIRO Publishing

Subject

General Chemistry

Link

http://www.publish.csiro.au/CH/pdf/CH9791395

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Epimanool and a New 2,6-Dideoxy-hexopyran-3-ulose Derivative from Celmisia viscosa;Natural Product Communications;2013-06

2. Podocarpane-to-spongian skeleton conversion. Synthesis of (+)-isoagatholactone and (–)-spongia-13(16),14-diene;J. Chem. Soc., Perkin Trans. 1;1996

3. Rin -Opening of Acetal III (8,13/13,17-Diepoxy-14,15-dinorlabdane) and the Synthesis of Potential Odorants Derived From Manool;Australian Journal of Chemistry;1994

4. Studies on the Synthesis of Scoparic Acid A and Related Labdane Diterpenoids. Synthesis of (E)-6β-Hydroxylabda-8-(17),13-dien-15-oic Acid;Journal of Natural Products;1993-12

5. Synthesis of (-)-borjatriol;The Journal of Organic Chemistry;1992-01

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