Lewis acid catalyzed formation of 3-amino-3-carboxy-tetrahydroquinoline derivatives via tandem 1,5-hydride transfer/cyclization process

Tetrahedron

Volumn 69, Issue 34, 2013, Pages 7019-7025

  Han, Wen Yong ^a,c   Zuo, Jian ^a,c   Wu, Zhi Jun ^b   Zhang, Xiao Mei ^a   Yuan, Wei Cheng ^a  

^a CHENGDU INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b CHENGDU INSTITUTE OF BIOLOGY   (China)

^c UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

(Z) Alkylidene azlactone; 1,5 Hydride transfer; Lewis acid; Spirocyclic skeleton; Tetrahydroquinolines

Indexed keywords

3 AMINO 3 CARBOXYTETRAHYDROQUINOLINE DERIVATIVE; HETEROCYCLIC COMPOUND; LEWIS ACID; QUINOLINE DERIVATIVE; SPIRO COMPOUND; UNCLASSIFIED DRUG;

1,5 HYDRIDE TRANSFER; ARTICLE; CATALYSIS; CHEMICAL REACTION; CYCLIZATION; DERIVATIZATION; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGEN BOND; METHODOLOGY; NUCLEAR OVERHAUSER EFFECT; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; STEREOCHEMISTRY;

EID: 84880133668     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.06.047     Document Type: Article

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