STEREOCHEMISTRY OF A UNIQUE TRICARBOCYCLIC COMPOUND PREPARED BY SUPERACID-CATALYZED CYCLIZATION

Authors
TANIMOTO H KIYOTA H ORITANI T MATSUMOTO K
Citation
H. Tanimoto et al., STEREOCHEMISTRY OF A UNIQUE TRICARBOCYCLIC COMPOUND PREPARED BY SUPERACID-CATALYZED CYCLIZATION, Synlett, (1), 1997, pp. 121
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
1
Year of publication
1997
Database
ISI
SICI code
0936-5214(1997):1<121:SOAUTC>2.0.ZU;2-V
Abstract
Chlorosulfonic acid catalyzed cyclization reaction of beta-monocyclone rolidol and beta-monocyclofarnesol and corresponding acetates gave a u nique rearranged product (2S, 3S*, 4aR*, 5,5,8a-tetramethyl-2H-2,4a-m ethanonaphthalen-3-ol, the structure of which was elucidated by X-ray analysis.