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Volumn 63, Issue 26, 2007, Pages 6035-6041

A highly regio- and stereo-selective [3+2] annulation of allylic compounds and 2-substituted 1,1-dicyanoalkenes through a catalytic carbon-phosphorus ylide reaction

Author keywords

2 Substituted 1,1 dicyanoalkenes; Allylic compounds; Carbon phosphorus ylide; Phosphine

Indexed keywords

1,1 DICYANOALKENE DERIVATIVE; ALKENE DERIVATIVE; ALLYL COMPOUND; CARBON; PHOSPHINE; PHOSPHORUS; UNCLASSIFIED DRUG;

EID: 34248659124     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.02.115     Document Type: Article
Times cited : (110)

References (25)
  • 1
    • 34248652556 scopus 로고    scopus 로고
    • For reviews on phosphine-catalyzed reactions, see:
  • 4
    • 34248678026 scopus 로고    scopus 로고
    • For recent reports on phosphine-catalyzed reactions, see:
  • 18
    • 0001173762 scopus 로고
    • For the use of 5a as the electrophilic olefin in [3+2] annulation reactions, see:
    • For the use of 5a as the electrophilic olefin in [3+2] annulation reactions, see:. Boivin J., Tailhan C., and Zard S.Z. J. Am. Chem. Soc. 113 (1991) 5874
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 5874
    • Boivin, J.1    Tailhan, C.2    Zard, S.Z.3
  • 19
    • 34248654224 scopus 로고    scopus 로고
    • For some stoichiometric examples of the change in the addition of γ-position of the ylide to the α-position, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.