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Volumn 40, Issue 50, 1999, Pages 8855-8858

Stereoselective total syntheses of α,β-unsaturated δ-lactones having a 1,3-syn-polyol moiety, isolated from Cryptocarya latifolia

Author keywords

1,3 polyol; Allylation; Lactone; Reduction; Sharpless asymmetric epoxidation

Indexed keywords

LACTONE DERIVATIVE;

EID: 0033544814     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01860-2     Document Type: Article
Times cited : (42)

References (24)
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  • 14
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    • note
    • The allyl alcohol 5 was prepared from 4 in four steps: (1) silylation by TBSCl, (2) DIBAH reduction, (3) the Horner-Wadsworth-Emmons reaction, and (4) DIBAH reduction (83% overall yield).
  • 19
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    • Minami, N.; Ko, S.; Kishi, Y. J. Am. Chem. Soc. 1982, 104, 1109; Ma. P.; Martin, V. S.; Masamune, S.; Sharpless, K. B.; Viti, S. M. J. Org. Chem. 1982, 47, 1378.
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    • Minami, N.1    Ko, S.2    Kishi, Y.3
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  • 23
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    • note
    • 3) δ 20.1, 21.1, 21.3, 29.2, 39.1, 40.4, 67.7, 67.7, 74.9, 121.4, 144.7, 163.7, 170.5, 170.6.
  • 24
    • 0009478798 scopus 로고    scopus 로고
    • note
    • 3) δ 19.9, 21.1, 21.1, 21.3, 29.1, 39.0, 40.0, 40.1, 67.6, 67.7, 68.1, 74.8, 121.3, 144.7, 163.7, 170.4, 170.5, 170.6.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.