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Volumn 31, Issue 16, 1990, Pages 2239-2242

A Direct Stereoselective Synthesis of (±)-14-Deoxyisoamijiol

Author keywords

[No Author keywords available]

Indexed keywords

14 DEOXYISOAMIJIOL; UNCLASSIFIED DRUG;

EID: 0025263985     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(90)80195-R     Document Type: Article
Times cited : (40)

References (34)
  • 8
    • 0000703744 scopus 로고
    • For a failed “A + C å ABC” strategy featuring an intramolecular Michael addition.
    • (1985) J. Org. Chem. , vol.50 , pp. 4102
    • Belmont1    Paquette2
  • 10
    • 84918638464 scopus 로고    scopus 로고
    • A manuscript discussing the diastereoselectivity of dienone cyclizations is in preparation.
  • 12
    • 84918618479 scopus 로고    scopus 로고
    • a, All structures drawn here represent racemates, only one enantiomer being drawn, b) Reaction conditions have not been optimized, c) All yields are isolated yields, b) The spectroscopic data obtained for all new compounds were consistent with the assigned structures.
  • 13
    • 0010660555 scopus 로고
    • Chloride 6 has been independently prepared via the identical sequence of reactions, see:
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2187
    • Akers1    Bryson2
  • 16
    • 84918616004 scopus 로고    scopus 로고
    • 13 as follows:
  • 22
    • 84918597083 scopus 로고    scopus 로고
    • 17 with cyclic allylsilanes demonstrated that electrophiles can also add syn to the silyl moiety. Note that the allylsilane of 2 reacts with anti selectivity, despite its cyclic nature.
  • 33
    • 84918634354 scopus 로고
    • For a comprehensive review, see:, J.D. Morrison, Academic Press, Inc, Orlando, Fla
    • (1984) Asymmetric Synthesis , vol.3 , pp. 554-558
    • Hill1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.