An efficient route to 2-substituted N-(1-amino-3-methylpyrrol)amides by ring-opening cyclization of benzylidene- and alkylidenecyclopropylcarbaldehydes with hydrazides

Journal of Organic Chemistry

Volumn 74, Issue 16, 2009, Pages 5983-5986

  Tang, Xiang Ying ^a   Shi, Min ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDES; AMINES; CHEMICAL REACTIONS;

BENZYLIDENE; CHEMICAL EQUATIONS; FIVE-MEMBERED RINGS; GOOD YIELD; IN-SITU; RING OPENING; SYNTHETIC METHODS;

REACTION RATES;

4 METHYL N(3 METHYL 2 PHENYL 1H PYRROL 1 YL)BENZENESULFONAMIDE; ALDEHYDE DERIVATIVE; BENZAMIDE DERIVATIVE; BENZYLIDENEACETONE; HYDRAZIDE DERIVATIVE; N(3 METHYL 2 PHENYL 1H PYRROL 1 YL)BENZAMIDE; UNCLASSIFIED DRUG; ALDEHYDE; AMIDE; BENZYLIDENE DERIVATIVE; HYDRAZINE; HYDRAZINE DERIVATIVE; PYRROLE DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CYCLIZATION; MOLECULAR MECHANICS; REACTION ANALYSIS; RING OPENING; SYNTHESIS; TEMPERATURE DEPENDENCE; CHEMISTRY;

ALDEHYDES; AMIDES; BENZYLIDENE COMPOUNDS; CYCLIZATION; HYDRAZINES; PYRROLES;

EID: 70349111856     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900730t     Document Type: Article

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