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Volumn 9, Issue 22, 2011, Pages 7913-7920

Cu(i)-catalyzed tandem benzyldiazoester coupling with terminal alkyne-allene formation-Michael reaction: Application to the syntheses of oxa and azacycles

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREO-SELECTIVITY; FUNCTIONALIZED; PRACTICAL PROCEDURES; TERMINAL ALKYNE;

EID: 80055015497     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob06128c     Document Type: Article
Times cited : (23)

References (33)
  • 30
    • 0027508436 scopus 로고
    • Compound 8 was prepared starting from l-(+) alanine in 3 steps, i.e. esterification followed by reduction, 2-carbon Wittig reaction and hydrogenation.
    • J. N. Tawara A. Blokhin T. A. Foderaro F. R. Stermitz J. Org. Chem. 1993 58 4813
    • (1993) J. Org. Chem. , vol.58 , pp. 4813
    • Tawara, J.N.1    Blokhin, A.2    Foderaro, T.A.3    Stermitz, F.R.4
  • 31
    • 0025899435 scopus 로고
    • The enantioselectivity and relative stereochemistry of the hydrogenated product 9 was determined in comparison with the sign and magnitude of the specific rotation of the piperidine alkaloid 13
    • Q. Meng M. Hesse Tetrahedron 1991 47 6251
    • (1991) Tetrahedron , vol.47 , pp. 6251
    • Meng, Q.1    Hesse, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.