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Volumn 64, Issue 52, 2008, Pages 11896-11907

Radical 1,4-aryl transfer in arylcarboxamides leading to phthalimides, biaryls and enantiomerically enriched β-arylethylamines

Author keywords

[No Author keywords available]

Indexed keywords

2 (2 PHENYLPROP 2 ENYL)ISOINDOLINE 1,3 DIONE; 5 METHOXY 2 [2 (4 METHOXYPHENYL)PROP 2 ENYL]ISOINDOLINE 1,3 DIONE; 5 METHYL 2 [2 (4 METHYLPHENYL)PROP 2 ENYL]ISOINDOLINE 1,3 DIONE; AMIDE; CARBAMIC ACID DERIVATIVE; ETHYLAMINE; N (2 BROMOPROP 2 ENYL) N (4 METHOXYBENZOYL) 4 METHOXYBENZAMIDE; N (2 BROMOPROP 2 ENYL) N (4 METHYLBENZOYL) 4 METHYLBENZAMIDE; N (2 BROMOPROP 2 ENYL) N [4 TRIFLUOROMETHYLBENZOYL] 4 TRIFLUOROMETHYLBENZAMIDE; N BENZOYL N (2 BROMOPROP 2 ENYL)BENZAMIDE; PHTHALIMIDE DERIVATIVE; TERT BUTYL BIPHENYL 2 YL N FORMYLCARBAMATE; TERT BUTYL N FORMYL(20 METHOXYBIPHENYL 2 YL)CARBAMATE; TERT BUTYL N FORMYL(30 METHOXYBIPHENYL 2 YL)CARBAMATE; TERT BUTYL N FORMYL(40-METHOXYBIPHENYL 2 YL)CARBAMATE; TERT BUTYL N FORMYL[40 TRIFLUOROMETHYLBIPHENYL 2 YL]CARBAMATE; UNCLASSIFIED DRUG;

EID: 56249110095     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.07.118     Document Type: Article
Times cited : (18)

References (83)
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    • Cyclisations at the ortho-position are 'endo' because the bond order between the ipso and ortho carbons is reduced during cyclisation; however, there is also an equivalent reduction in bond order between the ortho and meta carbons therefore imparting an exo element to the cyclisation. Some authors use '6-endo/exo' to indicate this; here the subscript Ar is used instead, and is also applied to the 5-exo cyclisations simply for consistency in notation.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.