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Volumn 52, Issue 3, 2000, Pages 1241-1249

Development of a method for the synthesis of α-substituted α,β- unsaturated lactones based on stille-type Pd-catalyzed carbonylation of (Z)- ω-iodoalkenols. An efficient and selective synthesis of (+)-hamabiwalactone B

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; HAMABIWALACTONE B; LACTONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034161889     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-99-s138     Document Type: Article
Times cited : (25)

References (18)
  • 3
    • 0000365487 scopus 로고    scopus 로고
    • (c) For a review containing many pertinent references published since 1992, see E. Negishi, J. Organomet. Chem., 1999, 576, 179.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 179
    • Negishi, E.1
  • 6
    • 0033553442 scopus 로고    scopus 로고
    • and other pertinent references therein
    • (c) A. Alimardanov and E. Negishi, Tetrahdron Lett., 1999, 40, 3839 and other pertinent references therein.
    • (1999) Tetrahdron Lett. , vol.40 , pp. 3839
    • Alimardanov, A.1    Negishi, E.2
  • 10
    • 0027454392 scopus 로고
    • For Pd-catalyzed cross coupling reactions of acyclic α-stannyl-α,β-unsaturated esters, see (a) J. I. Levin, Tetrahedron Lett., 1993, 34, 6211.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 6211
    • Levin, J.I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.