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Volumn 53, Issue 38, 2012, Pages 5180-5182

Ireland-Claisen rearrangement of ynamides: Stereocontrolled synthesis of 2-amidodienes

Author keywords

Amino acid; Furanomycin; Ireland Claisen; Rearrangement; Sigmatropic

Indexed keywords

2 AMIDODIENE DERIVATIVE; AMIDE; AMINO ACID; CARBOXYLIC ACID; UNCLASSIFIED DRUG;

EID: 84865172209     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.07.088     Document Type: Article
Times cited : (18)

References (47)
  • 11
    • 4344610661 scopus 로고    scopus 로고
    • For recent reviews concerning the Ireland-Claisen rearrangement, see: A.M. Castro Chem. Rev. 104 2004 2939
    • (2004) Chem. Rev. , vol.104 , pp. 2939
    • Castro, A.M.1
  • 14
    • 0000217402 scopus 로고
    • Claisen Rearrangements, Comprehensive Organic Synthesis
    • P. Wipf Claisen Rearrangements, Comprehensive Organic Synthesis B.M. Trost, I. Fleming, L.A. Paquette, Vol 5 1991 Pergamon Oxford 827
    • (1991) Vol 5 , pp. 827
    • Wipf, P.1
  • 26
    • 84865160380 scopus 로고
    • For the synthesis of α-allenyl-α-amino acids through the ester enolate Claisen rearrangement of α-amino propargyl esters, see: P. Casara, K. Jund, and P. Bey Tetrahedron Lett. 1984 1891 25
    • (1891) Tetrahedron Lett. , vol.1984 , pp. 25
    • Casara, P.1    Jund, K.2    Bey, P.3
  • 46
  • 47


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.