TY - JOUR
T1 - Stereochemistry of a Unique Tricarbocyclic Compound Prepared by Superacid-Catalyzed Cyclization
AU - Tanimoto, Hisahide
AU - Kiyota, Hiromasa
AU - Oritani, Takayuki
AU - Matsumoto, Keita
PY - 1997/12/1
Y1 - 1997/12/1
N2 - Chlorosulfonic acid catalyzed cyclization reaction of β-monocyclonerolidol and β-monocyclofarnesol and corresponding acetates gave a unique rearranged product (2S*, 3S*, 4aR*, 8aS*)-1, 3, 4, 5, 6, 7, 8, 8a-octahydro-2, 5, 5, 8a-tetramethyl-2H-2, 4a-methanonaphthalen-3-ol, the structure of which was elucidated by X-ray analysis.
AB - Chlorosulfonic acid catalyzed cyclization reaction of β-monocyclonerolidol and β-monocyclofarnesol and corresponding acetates gave a unique rearranged product (2S*, 3S*, 4aR*, 8aS*)-1, 3, 4, 5, 6, 7, 8, 8a-octahydro-2, 5, 5, 8a-tetramethyl-2H-2, 4a-methanonaphthalen-3-ol, the structure of which was elucidated by X-ray analysis.
UR - http://www.scopus.com/inward/record.url?scp=0010360515&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0010360515&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0010360515
VL - 1997
SP - 121
EP - 122
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 1
ER -