메뉴 건너뛰기




Volumn 6, Issue 4, 2015, Pages 2196-2201

Enantioselective cis-β-lactam synthesis by intramolecular C-H functionalization from enoldiazoacetamides and derivative donor-acceptor cyclopropenes

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLATION; REACTION INTERMEDIATES;

EID: 84925013776     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c4sc03991b     Document Type: Article
Times cited : (80)

References (67)
  • 60
    • 2942600196 scopus 로고    scopus 로고
    • Nonpolar solvents provide a significant increase in the enantioselectivity in some metal carbene reactions, for example, 2,2-DMB and TBME have previously been demonstrated to be an optimal solvent for enantioselective C-H functionalization and other metal carbene transformations
    • P. Müller G. Bernardinelli Y. F. Allenbach M. Ferry H. D. Flack Org. Lett. 2004 6 1725
    • (2004) Org. Lett. , vol.6 , pp. 1725
    • Müller, P.1    Bernardinelli, G.2    Allenbach, Y.F.3    Ferry, M.4    Flack, H.D.5
  • 64
    • 51049091002 scopus 로고    scopus 로고
    • 1H NMR coupling constants, see ref. 14e: generally cis = 5-8 Hz; trans = 0-2 Hz.
    • M. Díaz-Requejo P. J. Pérez Chem. Rev. 2008 108 3379
    • (2008) Chem. Rev. , vol.108 , pp. 3379
    • Díaz-Requejo, M.1    Pérez, P.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.