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Volumn , Issue 5, 1998, Pages 763-770

An improved dienophile-induced access to enantiopure 2,4-dideoxysugar lactones via hetero Diels-Alder reaction: Synthesis of the (+)-lactone moiety of compactin

Author keywords

(+) Compactin lactone; (4+2) Heterocycloaddition; Chiral enol ethers; Intramolecular Mitsunobu reaction; Methyl (E) tert butoxymethylenepyruvate

Indexed keywords

COMPACTIN; LACTONE DERIVATIVE;

EID: 0031976968     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-4489     Document Type: Article
Times cited : (45)

References (33)
  • 17
    • 0027430833 scopus 로고
    • 5c careful control of the reaction temperature prevented any decarbonylation into acryloyl derivative previously observed at higher temperatures. See also Tietze, L. F.; Schneider, C.; Pretor, M. Synthesis 1993, 1079.
    • (1993) Synthesis , pp. 1079
    • Tietze, L.F.1    Schneider, C.2    Pretor, M.3
  • 19
    • 34548372444 scopus 로고    scopus 로고
    • note
    • Extensive work focused on optimization of facial control using ethyl, isopropyl or benzyl ester analogs of 3a,b or hexahydromandelic derivative of 3b gave no improvement.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.