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Volumn 40, Issue 3, 1999, Pages 431-434

A highly efficient and selective synthesis of lissoclinolide featuring hydrogen transfer hydrozirconation, trans-selective Pd-catalyzed cross coupling of alkenylzirconiums with 1,1-dibromoalkenes and Ag-catalyzed lactonization providing (Z)-γ-alkylidenebutenolides

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; ANTIBIOTIC AGENT; BROMINE DERIVATIVE; LISSOCLINOLIDE; PALLADIUM; UNCLASSIFIED DRUG; ZIRCONIUM DERIVATIVE;

EID: 0033555262     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02394-6     Document Type: Article
Times cited : (111)

References (24)
  • 7
    • 0001216247 scopus 로고
    • the reaction was significantly more complicated by some side reactions, such as competitive formation of pyranones, and conjugate substitution via Heck reaction. Even under the optimized conditions, however, homodimerization of alkynes may still be a significant side reaction [1b,1c]
    • 3 was used [Lambert C, Utimoto K, Nozaki H. Tetrahedron Lett. 1984; 25: 5323], the reaction was significantly more complicated by some side reactions, such as competitive formation of pyranones, and conjugate substitution via Heck reaction. Even under the optimized conditions, however, homodimerization of alkynes may still be a significant side reaction [1b,1c].
    • (1984) Tetrahedron Lett. , vol.25 , pp. 5323
    • Lambert, C.1    Utimoto, K.2    Nozaki, H.3
  • 23
    • 0030743260 scopus 로고    scopus 로고
    • Panek JS; Hu T. J. Org. Chem. 1997; 62: 4912. Note added in proof: After submission of this manuscript a paper reporting a different but related synthesis of lissoclinolide was brought to our attention [Rossi R, Bellina F, Biagetti M, Mannina L. Tetrahedron Lett. 1998; 39: 7799].
    • (1997) J. Org. Chem. , vol.62 , pp. 4912
    • Panek, J.S.1    Hu, T.2
  • 24
    • 0032532252 scopus 로고    scopus 로고
    • Panek JS; Hu T. J. Org. Chem. 1997; 62: 4912. Note added in proof: After submission of this manuscript a paper reporting a different but related synthesis of lissoclinolide was brought to our attention [Rossi R, Bellina F, Biagetti M, Mannina L. Tetrahedron Lett. 1998; 39: 7799].
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7799
    • Rossi, R.1    Bellina, F.2    Biagetti, M.3    Mannina, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.