Diastereoselective routes towards the austrodorane skeleton based on pinacol rearrangement: synthesis of (+)-austrodoral and (+)-austrodoric acid-Reference-Cited by-同舟云学术

Diastereoselective routes towards the austrodorane skeleton based on pinacol rearrangement: synthesis of (+)-austrodoral and (+)-austrodoric acid

Published:2007-11 Issue:48 Volume:63 Page:11943-11951
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Alvarez-Manzaneda Enrique,Chahboun Rachid,Barranco Inmaculada,Cabrera Eduardo,Alvarez Esteban,Lara Armando,Alvarez-Manzaneda Ramón,Hmamouchi Mohamed,Es-Samti Hakima

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference36 articles.

1. Austrodoral and austrodoric acid: nor-sesquiterpenes with a new carbon skeleton from the Antarctic nudibranch Austrodoris kerguelenensis

2. Norrisolide, a novel diterpene from the dorid nudibranch Chromodoris norrisi

3. Three New norrisolide related rearranged spongians

4. Chromodorolide A, a rearranged diterpene with a new carbon skeleton from the Indian Ocean nudibranch Chromodoris cavae

5. Chromodorane diterpenes from the tropical dorid nudibranch Chromodoris cavae

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