Anionically induced domino reactions; synthesis of analogues of marine sesquiterpenes

Authors
Gutke, HJ Oesterreich, K Spitzner, D Braun, NA
Citation
Hj. Gutke et al., Anionically induced domino reactions; synthesis of analogues of marine sesquiterpenes, TETRAHEDRON, 57(6), 2001, pp. 997-1003
Citations number
34
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
57
Issue
6
Year of publication
2001
Pages
997 - 1003
Database
ISI
SICI code
0040-4020(20010204)57:6<997:AIDRSO>2.0.ZU;2-O
Abstract
An anionically induced domino reaction is the key step in the synthesis of the isotwistane skeleton. This precursor can be transformed into the marine sesquiterpene 2-isocyanopupukeanane or its structural analogues. (C) 2001 Elsevier Science Ltd. All rights reserved.