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Volumn 4, Issue 9, 2002, Pages 1543-1546

Diastereoselective Synthesis of the endo- and exo-Spirotetronate Subunits of the Quartromicins. The First Enantioselective Diels - Alder Reaction of an Acyclic (Z)-1,3-Diene

Author keywords

[No Author keywords available]

Indexed keywords

FURAN DERIVATIVE; QUARTROMICIN; SPIRO COMPOUND;

EID: 0037007705     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol025772+     Document Type: Article
Times cited : (43)

References (24)
  • 1
    • 0041357861 scopus 로고    scopus 로고
    • note
    • A portion of this work was performed by D. A. Barda at Indiana Unversity.
  • 12
    • 0041357860 scopus 로고    scopus 로고
    • note
    • We use the terms "endo" and "exo" to describe the stereochemistry of the spirotetronate substructures in recognition of the fact that 1 and 2, at least formally, can be synthesized from the products of endo- or exo-Diels-Alder reactions of diene 3 and an α-acetoxyacrylate dienophile, respectively.
  • 14
    • 0026748480 scopus 로고
    • Marshall reported a sequence analogous to our conversion of 10 to 14 in his synthesis of the top half of kijanolide: Marshall, J. A.; Xie, S. J. Org. Chem. 1992, 57, 2987.
    • (1992) J. Org. Chem. , vol.57 , pp. 2987
    • Marshall, J.A.1    Xie, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.