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Volumn 48, Issue 23, 1992, Pages 4677-4686

A one-flask multicomponent annulation reaction as the key step in a total synthesis of spirobicyclic (±)-β-vetivone

Author keywords

[No Author keywords available]

Indexed keywords

BETA VETIVONE; SESQUITERPENE; SPIRO COMPOUND; UNCLASSIFIED DRUG;

EID: 0026625830     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)81566-0     Document Type: Article
Times cited : (25)

References (62)
  • 5
    • 0344369944 scopus 로고
    • Sequential Michael-Michael-Ring Closure reactions for 3-different-component, one-pot, 2+2+2 construction of acylcyclohexenes and an acylcyclohexanol
    • (1986) Tetrahedron Letters , vol.27 , pp. 659
    • Posner1    Lu2    Asirvatham3
  • 6
  • 24
    • 0000050010 scopus 로고
    • For an asymmetric total synthesis of (−)-β-vetivone, see, and references therein.
    • (1988) J. Org. Chem. , vol.53 , pp. 6031
    • Posner1    Hamill2
  • 35
    • 84913063003 scopus 로고
    • Synthetic utility of a fluorine-facilitated Claisen rearrangement: a novel synthetic method for 2,4-alkadienoic acids using 2,2,2-trifluoroethyl phenyl sulfoxide.
    • (1981) Chemistry Letters , pp. 1289
    • Nakai1    Tanaka2    Ogasaware3    Ishikawa4
  • 44
    • 84909451416 scopus 로고
    • Organocopper(I) Compounds and Organocuprates in Synthesis
    • For general organocopper reviews including copper catalyzed conjugate additions see
    • (1972) Synthesis , pp. 63
    • Normant1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.