SCOPUS 정보 검색 플랫폼

Volumn 12, Issue 7, 2014, Pages 1057-1060

Enantioselective organocatalytic oxa-Michael addition of oximes to β-CF3-β-disubstituted nitroalkenes: Efficient synthesis of β-amino-α-trifluoromethyl alcohols

(7) Liu, Feng Lei a,b Chen, Jia Rong a,b Feng, Bin a,b Hu, Xiao Qiang a,b Ye, Li Hua a,b Lu, Liang Qiu a,b Xiao, Wen Jing a,b

a CENTRAL CHINA NORMAL UNIVERSITY (China)

b School of Pharmaceutical Science and Technology (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; BIOCHEMISTRY;

BI-FUNCTIONAL; CINCHONA ALKALOID; EFFICIENT SYNTHESIS; ENANTIOSELECTIVE; HIGH ENANTIOSELECTIVITY; ORGANOCATALYTIC; OXA-MICHAEL ADDITION; TRIFLUOROMETHYL;

ENANTIOSELECTIVITY;

ALKENE; AMINOALCOHOL; NITRO DERIVATIVE; OXIME;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ALKENES; AMINO ALCOHOLS; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; MODELS, MOLECULAR; MOLECULAR STRUCTURE; NITRO COMPOUNDS; OXIMES; STEREOISOMERISM;

EID: 84892916419 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c3ob42329h Document Type: Article

Times cited : (34)

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