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Volumn 7, Issue 15, 2005, Pages 3371-3373

Asymmetric synthesis of (-)-dihydroxanthatin by the stereoselective Oshima-Utimoto reaction

Author keywords

[No Author keywords available]

Indexed keywords

11,13 DIHYDROXANTHATIN; 11,13-DIHYDROXANTHATIN; FURAN DERIVATIVE;

EID: 23044503277     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051276k     Document Type: Article
Times cited : (66)

References (34)
  • 4
    • 23044495574 scopus 로고    scopus 로고
    • see ref 1
    • (c) For a review of approaches to the synthesis of α-methylene butyrolactones, see ref 1.
  • 20
    • 0025942580 scopus 로고
    • For application of this process to cyclic substrates, see: (f) Larock, R. C.; Lee, N. H. J. Am. Chem. Soc. 1991, 113, 7815.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7815
    • Larock, R.C.1    Lee, N.H.2
  • 30
    • 0002652021 scopus 로고
    • For a review that includes the stereoselection in the alkylation of butyrolactones, see: Evans, D. A. Asymmetric Synthesis 1984, 3, 1.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 1
    • Evans, D.A.1
  • 31
    • 23044474838 scopus 로고    scopus 로고
    • note
    • ,2-Stereoinduction in the alkylation at C3 appears to result from interaction with substituents at C4, with the C4 hydrogen better aligned to interact with the incoming nucleophile as compared to the C4 alkyl group.
  • 33
    • 1842483218 scopus 로고    scopus 로고
    • For a review of enyne metathesis, see: (b) Diver, S. T.; Giessert, A. Chem. Rev. 2004, 104, 1317.
    • (2004) Chem. Rev. , vol.104 , pp. 1317
    • Diver, S.T.1    Giessert, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.