Synthesis of substituted 1,8-naphthyridine-3-carboxylates from Baylis-Hillman adducts of substituted 2-chloronicotinaldehydes

Helvetica Chimica Acta

Volumn 92, Issue 5, 2009, Pages 959-966

  Narender, Puli ^a   Ravinder, Mettu ^a   Sadhu, Partha Sarathi ^a   Raju, Bhimapaka China ^a   Ramesh, Chilukuri ^b   Rao, Vaidya Jayathirtha ^a,b  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

^b NATIONAL INSTITUTE OF PHARMACEUTICAL EDUCATION AND RESEARCH NIPER   (India)

Author keywords

[No Author keywords available]

Indexed keywords

BAYLIS-HILLMAN ADDUCTS; NAPHTHYRIDINE;

SYNTHESIS (CHEMICAL);

CARBOXYLATION;

6 ETHYL 2 METHYL 1,8 NAPHTHYRIDINE 2,6 DICARBOXYLATE; ALDEHYDE DERIVATIVE; AZIDE; CARBOXYLIC ACID DERIVATIVE; DIMETHYL 1,8 NAPHTHYRIDINE 2,6 DICARBOXYLATE; ETHYL 2 (AZIDOMETHYL) 3 (2 CHLORO 5 METHYLPYRIDIN 3 YL)PROP 2 ENOATE; ETHYL 6 ETHYL 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; ETHYL 6 METHYL 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; ETHYL 6 METHYL 7 PHENYL 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; ETHYL 6 PHENYL 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; METHYL 2 (AZIDOMETHYL) 3 (2 CHLORO 5 METHYL 6 PHENYLPYRIDIN 3 YL)PROP 2 ENOATE; METHYL 2 (AZIDOMETHYL) 3 (2 CHLORO 5 METHYLPYRIDIN 3 YL)PROP 2 ENOATE; METHYL 3 (2 CHLORO 5 METHYLPYRIDIN 3 YL) 2 (HYDROXYMETHYL)PROP 2 ENOATE; METHYL 5 [2 (AZIDOMETHYL) 3 ETHOXY 3 OXOPROP 1 EN 1 YL] 6 CHLOROPYRIDINE 2 CARBOXYLATE; METHYL 5 [2 (AZIDOMETHYL) 3 METHOXY 3 OXOPROP 1 EN 1 YL] 6 CHLOROPYRIDINE 2 CARBOXYLATE; METHYL 6 (4 METHOXYPHENYL) 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; METHYL 6 ETHYL 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; METHYL 6 METHYL 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; METHYL 6 METHYL 7 PHENYL 1,8 NAPHTHYRIDINE 3 CARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; BAYLIS HILLMAN REACTION; CONTROLLED STUDY; DRUG SYNTHESIS; PRIORITY JOURNAL; REDUCTION;

EID: 66949166794     PISSN: 0018019X     EISSN: None     Source Type: Journal    
DOI: 10.1002/hlca.200800352     Document Type: Article

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