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Volumn 50, Issue 2, 1994, Pages 475-486

A novel method for stereospecific generation of natural C-17 stereochemistry and either C-20 epimer in steroid side chains by palladium-catalyzed hydrogenolysis of C-17 and C-20 allylic carbonates.

Author keywords

[No Author keywords available]

Indexed keywords

STEROID;

EID: 0028158805     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)80769-9     Document Type: Article
Times cited : (24)

References (52)
  • 7
    • 0005983928 scopus 로고
    • A new Claisen approach to the stereospecific introduction of a steroid side chain at C-20. A simple synthesis of 20-epicholesterol via the .BETA.-face rearrangement.
    • (1985) Chemistry Letters , pp. 115
    • Mikami1    Kawamoto2    Nakai3
  • 26
    • 0010263147 scopus 로고
    • Regioselective synthesis of 1-olefins by palladium-catalyzed hydrogenolysis of terminal allylic compounds with ammonium formate.
    • (1984) Chemistry Letters , pp. 1017
    • Tsuji1    Shimizu2    Minami3
  • 27
    • 84987088818 scopus 로고
    • Preparation of 1-Alkenes by the Palladium-Catalyzed Hydrogenolysis of Terminal Allylic Carbonates and Acetates with Formic Acid-Triethylamine
    • (1986) Synthesis , pp. 623
    • Tsuji1    Minami2    Shimizu3
  • 49
    • 0004009372 scopus 로고
    • The stereochemical terms of “syn” and “anti” are related to the middle hydrogen on C-2 in a π-allyl system. see;, 5th edition, Wiley Interscience Publishers, New York
    • (1988) Advanced Inorganic Chemistry , pp. 77
    • Cotton1    Wilkinson2
  • 52
    • 0000298103 scopus 로고
    • Generation of Tertiary Phosphine-Coordinated Pd(0) Species from Pd(OAc)2 in the Catalytic Heck Reaction.
    • (1992) Chemistry Letters , pp. 2177
    • Ozawa1    Kubo2    Hayashi3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.