Copper-mediated oxidative transformation of N-allyl enamine carboxylates toward synthesis of azaheterocycles

Journal of the American Chemical Society

Volumn 136, Issue 16, 2014, Pages 6011-6020

  Toh, Kah Kah ^a   Biswas, Anup ^a   Wang, Yi Feng ^a   Tan, Yun Yun ^a   Chiba, Shunsuke ^a  

^a Nanyang Technological University   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMISTRY; SYNTHESIS (CHEMICAL);

AZA-HETEROCYCLES; CYCLOPROPANATION; DIASTEREOSELECTIVE REDUCTION; ENAMINES; INTRAMOLECULAR CYCLOPROPANATIONS; OXIDATIVE TRANSFORMATIONS; REACTION CONDITIONS; RING OPENING;

CARBOXYLATION;

3 AZABICYCLO[3.1.0]HEX 2 ENE DERIVATIVE; 3 AZABICYCLO[3.1.0]HEXANE DERIVATIVE; 5 SUBSTITUTED 3 AZABICYCLO[3.1.0]HEX 2 ENE DERIVATIVE; ALKENE DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; COPPER; CYCLOPROPANE; HEXANE; N ALLYL ENAMINE CARBOXYLATE DERIVATIVE; UNCLASSIFIED DRUG; ALKENE; AMINE; CARBOXYLIC ACID; HETEROCYCLIC COMPOUND; PYRIDINE; PYRIDINE DERIVATIVE;

ARTICLE; SYNTHESIS; CATALYSIS; CHEMISTRY; ENZYME SPECIFICITY; OXIDATION REDUCTION REACTION; STEREOISOMERISM;

ALKENES; AMINES; CARBOXYLIC ACIDS; CATALYSIS; CHEMISTRY TECHNIQUES, SYNTHETIC; COPPER; HETEROCYCLIC COMPOUNDS; OXIDATION-REDUCTION; PYRIDINES; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 84899583974     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja500382c     Document Type: Article

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