Synthesis of (S)-7-amino-5-azaspiro[2.4]heptane via highly enantioselective hydrogenation of protected ethyl 1-(2-aminoaceto)cyclopropanecarboxylates

Journal of Organic Chemistry

Volumn 76, Issue 8, 2011, Pages 2807-2813

  Yao, Ying ^a   Fan, Weizheng ^a   Li, Wanfang ^a   Ma, Xin ^a   Zhu, Lvfeng ^b   Xie, Xiaomin ^a   Zhang, Zhaoguo ^a,c  

^a SHANGHAI JIAO TONG UNIVERSITY   (China)

^b NANJING UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^c SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBACTERIAL AGENT; ASYMMETRIC HYDROGENATION; CYCLOPROPANECARBOXYLATES; ENANTIOSELECTIVE HYDROGENATION; ENANTIOSELECTIVE SYNTHESIS; HIGH ENANTIOSELECTIVITY; QUINOLONES;

BENZENE; CARBOXYLATION; ENANTIOSELECTIVITY; HEPTANE; PROPANE; RUTHENIUM COMPOUNDS;

HYDROGENATION;

7 AMINO 5 AZASPIRO[2.4]HEPTANE; CARBOXYLIC ACID DERIVATIVE; ETHYL 1 (2 AMINOACETO)CYCLOPROPANECARBOXYLATE; OLAMUFLOXACIN; QUINOLINE DERIVED ANTIINFECTIVE AGENT; SITAFLOXACIN; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOSELECTIVITY; HYDROGENATION;

ANTI-BACTERIAL AGENTS; AZA COMPOUNDS; CATALYSIS; CYCLOPROPANES; GLYCINE; HEPTANES; HYDROGENATION; MOLECULAR STRUCTURE; PHOSPHINES; QUINOLONES; RUTHENIUM; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 79953850785     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo2002165     Document Type: Article

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