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Journal of Organic Chemistry

Volumn 73, Issue 20, 2008, Pages 8089-8092

Ring-enlargement of dimethylaminopropenoyl cyclopropanes: An efficient route to substituted 2,3-dihydrofurans

(5) Zhang, Rui a Liang, Yongjiu a Zhou, Guangyuan a Wang, Kewei b Dong, Dewen a,b

a CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY (China)

b NORTHEAST NORMAL UNIVERSITY (China)

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID; ACIDS; CHEMICAL REACTIONS; ETHANOL; KETONES; PROPANE; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

AMMONIUM ACETATE; CHEMICAL EQUATIONS; DIHYDROFURANS; EFFICIENT SYNTHESIS;

AMMONIUM COMPOUNDS;

1 DIMETHYLAMINOPROPENOYL 1 BENZOYL CYCLOPROPANE; 1 DIMETHYLAMINOPROPENOYL CYCLOPROPANE; 2,3 DIHYDROFURAN DERIVATIVE; 2,3 DIHYDROFURO[3,2 C]PYRIDIN 4(5H) ONE; ACETIC ACID; ALCOHOL; AMMONIUM ACETATE; CYCLOPROPANE DERIVATIVE; FURAN DERIVATIVE; SODIUM HYDROXIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

ACETATES; ACETIC ACID; CATALYSIS; CYCLOPROPANES; FURANS; STEREOISOMERISM;

EID: 53849109210 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo801289p Document Type: Article

Times cited : (63)

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