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Total synthesis of (±)-herbertenediol
A. Srikrishna,
Published in
2006
Volume: 62
   
Issue: 12
Pages: 2892 - 2900
Abstract
A formal total synthesis of the sesquiterpene (±)-herbertenediol and its dimers mastigophorenes A-D has been accomplished, starting from vanillin via 2,3-dimethoxy-5-methylbenzaldehyde. A combination of Claisen rearrangement and ring-closing metathesis reactions were employed for the generation of the two vicinal quaternary carbons on a cyclopentane ring. © 2006 Elsevier Ltd. All rights reserved.
About the journal
JournalTetrahedron
ISSN00404020