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Volumn 135, Issue 43, 2013, Pages 16074-16077

Simple catalytic mechanism for the direct coupling of α-carbonyls with functionalized amines: A one-step synthesis of plavix

Author keywords

[No Author keywords available]

Indexed keywords

AMINE SUBSTRATES; CATALYTIC MECHANISMS; COPPER CATALYSIS; DIRECT COUPLING; FRAGMENT COUPLING; NUCLEOPHILIC DISPLACEMENT; ONE STEP SYNTHESIS; PHARMACEUTICAL AGENTS;

EID: 84887037627     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4096472     Document Type: Article
Times cited : (177)

References (43)
  • 40
    • 0037241494 scopus 로고    scopus 로고
    • The substituted enolate derived from 2-butanone is substantially more π-nucleophilic, a feature that likely contributes to selective bromination and thereafter amination at the butanone 3-position. Mayr nucleophile index values for enol silanes are consistent with this finding - 77
    • The substituted enolate derived from 2-butanone is substantially more π-nucleophilic, a feature that likely contributes to selective bromination and thereafter amination at the butanone 3-position. Mayr nucleophile index values for enol silanes are consistent with this finding: Mayr, H.; Kempf, B.; Ofial, A. R. Acc. Chem. Res. 2003, 36, 66-77
    • (2003) Acc. Chem. Res. , vol.36 , pp. 66
    • Mayr, H.1    Kempf, B.2    Ofial, A.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.