Stereochemistry of a Unique Tricarbocyclic Compound Prepared by Superacid-Catalyzed Cyclization

Hisahide Tanimoto, Hiromasa Kiyota, Takayuki Oritani, Keita Matsumoto

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)121-122
Number of pages2
JournalSynlett
Volume1997
Issue number1
Publication statusPublished - 1997
Externally publishedYes

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Stereochemistry
Cyclization
X ray analysis
Acetates
chlorosulfonic acid

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Stereochemistry of a Unique Tricarbocyclic Compound Prepared by Superacid-Catalyzed Cyclization. / Tanimoto, Hisahide; Kiyota, Hiromasa; Oritani, Takayuki; Matsumoto, Keita.

In: Synlett, Vol. 1997, No. 1, 1997, p. 121-122.

Research output: Contribution to journalArticle

Tanimoto, H, Kiyota, H, Oritani, T & Matsumoto, K 1997, 'Stereochemistry of a Unique Tricarbocyclic Compound Prepared by Superacid-Catalyzed Cyclization', Synlett, vol. 1997, no. 1, pp. 121-122.
Tanimoto, Hisahide ; Kiyota, Hiromasa ; Oritani, Takayuki ; Matsumoto, Keita. / Stereochemistry of a Unique Tricarbocyclic Compound Prepared by Superacid-Catalyzed Cyclization. In: Synlett. 1997 ; Vol. 1997, No. 1. pp. 121-122.
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