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Volumn 43, Issue 21, 1987, Pages 5055-5072

Stereochemical control of nature's biosynthetic pathways:A general strategy for the synthesis 0f polypropionate-derived structural units from a single chiral progenitor

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EID: 0000905924     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)87683-3     Document Type: Article
Times cited : (109)

References (83)
  • 8
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    • Iterative butenolide construction of polypropionate chains. Application to an efficient synthesis of (+)(9S)-dihydroerythronolide A
    • For some recent examples, see
    • (1987) Pure and Applied Chemistry , vol.59 , pp. 345
    • Stork1    Rychnovsky2
  • 28
    • 0019408557 scopus 로고
    • Asymmetric total synthesis of erythromcin. 1. Synthesis of an erythronolide A secoacid derivative via asymmetric induction
    • For some examples of the utilization of carbocyclic and heterocyclic templates, see
    • (1985) Journal of the American Chemical Society , vol.103 , pp. 3210
    • Woodward1
  • 29
    • 0019439350 scopus 로고
    • Asymmetric total synthesis of erythromycin. 2. Synthesis of an erythronolide A lactone system
    • For some examples of the utilization of carbocyclic and heterocyclic templates, see
    • (1985) Journal of the American Chemical Society , vol.103 , pp. 3213
    • Woodward1
  • 30
    • 0019440449 scopus 로고
    • Asymmetric total synthesis of erythromycin. 3. Total synthesis of erythromycin
    • For some examples of the utilization of carbocyclic and heterocyclic templates, see
    • (1985) Journal of the American Chemical Society , vol.103 , pp. 3215
    • Woodward1
  • 37
    • 0013538592 scopus 로고
    • Preparation of Some 2,3-Dideoxylactones by an Unusual Catalytic Hydrogenolysis
    • For the synthesis of butenolides see, ref. 6
    • (1986) Synthesis , pp. 1052
    • Lundt1    Pedersen2
  • 42
  • 46
    • 84918483885 scopus 로고    scopus 로고
    • For an independent approach to the construction of polypropionate subunits from a butenolide template, see ref. 3a.
  • 52
  • 54
  • 64
    • 0023125933 scopus 로고
    • For recent synthetic approaches to various subunits of ionomycin, see ref. 7; see also
    • (1987) Tetrahedron Lett. , vol.28 , pp. 731
    • Spino1    Weiler2
  • 66
    • 33845377284 scopus 로고
    • For recent synthetic approaches to various subunits of ionomycin, see ref. 7; see also
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 5303
    • Schreiber1    Wang2
  • 68
    • 0021252586 scopus 로고
    • For recent synthetic approaches to various subunits of ionomycin, see ref. 7; see also
    • (1984) J. Org. Chem. , vol.49 , pp. 2582
    • Wuts1    D'Costa2    Butler3
  • 75
    • 0001814788 scopus 로고
    • Synthetic Approaches toward Verrucarin A. Chiral Synthesis of (—)-Verrucarinolactone
    • (1982) HETEROCYCLES , vol.17 , pp. 311
    • Tomioka1    Sato2    Koga3
  • 81
    • 0001545645 scopus 로고
    • Synthetic studies on lignan lactones: aryl dithiane route to (.+-.)-podorhizol and (.+-.)-isopodophyllotoxone and approaches to the stegane skeleton
    • For some examples of utilization of butenolides in natural product synthesis, see ref. 6,7,8f,9,10; see also
    • (1973) The Journal of Organic Chemistry , vol.43 , pp. 985
    • Ziegler1    Scwharz2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.