Superacidic cyclization of all-trans-omega-acetoxyfarnesyl benzyl ether

Authors
Kulcitki, V Ungur, N Vlad, PF Gavagnin, M Castelluccio, F Cimino, G
Citation
V. Kulcitki et al., Superacidic cyclization of all-trans-omega-acetoxyfarnesyl benzyl ether, SYNTHESIS-S, (3), 2000, pp. 407-410
Citations number
12
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
SYNTHESIS-STUTTGART
ISSN journal
00397881 → ACNP
Issue
3
Year of publication
2000
Pages
407 - 410
Database
ISI
SICI code
0039-7881(200003):3<407:SCOABE>2.0.ZU;2-7
Abstract
The superacidic cyclization of all-trans-omega-acetoxyfarnesyl benzyl ether 2 begins at the internal double bond giving a mixture of diastereomeric mo nocyclic compounds 5 and 6, prenylated at gem-dimethyl groups.