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Tetrahedron Letters
Volumn 20, Issue 20, 1979, Pages 1783-1786
Stereospecific 2-vinylcyclohexanol formation via internal attack of an allylsilane moiety on an aldehyde group
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EID: 49249153344     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)86217-1     Document Type: Article
Times cited : (28)
References (31)
  • 10
    • 84917990952 scopus 로고
    • The effective use of the silylated compounds for the termination of the acid-induced syclization has been reported.Allylsilane for termination:
    • (1976) J. C. S. Chem. Comm. , pp. 183
    • Fleming1    Pearce2
  • 15
    • 84917990951 scopus 로고    scopus 로고
    • 4NF, 0° 10 min in THF, gave a complex mixture and the ratio was not determined.
  • 17
    • 84917990950 scopus 로고    scopus 로고
    • 28OSSi 320.163).
  • 18
    • 84917990949 scopus 로고    scopus 로고
    • 2).
  • 19
    • 84917990948 scopus 로고    scopus 로고
    • 28OSSi 320.163).
  • 20
    • 84917990947 scopus 로고    scopus 로고
    • 2).
  • 21
    • 84986680614 scopus 로고
    • A Highly Stereoselective Preparation ofl-Isopulegol
    • and references cited therein.
    • (1978) Synthesis , pp. 147
    • Nakatani1    Kawashima2
  • 24
    • 84917990946 scopus 로고    scopus 로고
    • We are tempted to explain the observed stereoselectivity by favouring the transition state A and B.
  • 25
    • 0000792398 scopus 로고
    • 3), 2.17 (m, 1H, signal partially superimposed on ring protons, CH-C=O), 3.60 (m, 1H, CH-O-).
    • (1965) J. Org. Chem. , vol.30 , pp. 3475
    • Marshall1    Cohen2
  • 31
    • 84917990945 scopus 로고    scopus 로고
    • Financial support by the Ministry of Education, Japanese Government, (Grant-in-Aid #303023) is acknowledged.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.