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Volumn 68, Issue 52, 2012, Pages 10794-10805

Synthesis of polycyclic β-lactams. Evolution of tertiary radicals generated by Cp2TiCl from 1,5- and 1,6-epoxynitriles

Author keywords

Epoxymonolactams; Methylbenzocarbacephems; Radical cyclisation; Tertiary homobenzyl radicals; Titanocene monochloride

Indexed keywords

ALKYL GROUP; AMIDE; BENZENE DERIVATIVE; BENZYL DERIVATIVE; BETA LACTAM DERIVATIVE; CARBACEPHEM DERIVATIVE; EPOXIDE; HYDROGEN; HYDROXYL GROUP; METHYL GROUP; NITRILE; POLYCYCLIC AROMATIC COMPOUND; RADICAL; TITANIUM DERIVATIVE;

EID: 84869490809     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.11.015     Document Type: Article
Times cited : (7)

References (109)
  • 8
    • 0345458279 scopus 로고
    • The numbering of the bi- and tricyclic β-lactams is given according to the IUPAC rules ()
    • The numbering of the bi- and tricyclic β-lactams is given according to the IUPAC rules (Pure Appl. Chem. 67 1995 1307 1375)
    • (1995) Pure Appl. Chem. , vol.67 , pp. 1307-1375
  • 31
    • 0004269715 scopus 로고    scopus 로고
    • P. Renaud, M.P. Sibi, Wiley-VCH Weinheim Chapter 3.3
    • T.V. RajanBabu P. Renaud, M.P. Sibi, Radicals in Organic Synthesis Vol. 2 2001 Wiley-VCH Weinheim Chapter 3.3
    • (2001) Radicals in Organic Synthesis , vol.2
    • Rajanbabu, T.V.1
  • 101
    • 84870809333 scopus 로고    scopus 로고
    • Preferred conformations for the studied compounds were derived form the ChemBio3D software (version 12.0, 2009. Cambridge Soft Corporation, USA) using MMFF94 force field calculations
    • Preferred conformations for the studied compounds were derived form the ChemBio3D software (version 12.0, 2009. Cambridge Soft Corporation, USA) using MMFF94 force field calculations.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.