Studies on the reduction of the nitro group in 3-aryl-2-methylene-4-nitro-alkanoates afforded by the Baylis-Hillman adducts: synthesis of 4-aryl-3-methylene-2-pyrrolidinones and 3-(1-alkoxycarbonyl-vinyl)-1H-indole-2-carboxylates

Tetrahedron

Volumn 62, Issue 43, 2006, Pages 10100-10110

  Singh, Vijay ^a   Kanojiya, Sanjeev ^a   Batra, Sanjay ^a  

^a CENTRAL DRUG RESEARCH INSTITUTE   (India)

Author keywords

1H Indole 2 carboxylate; 2 Pyrrolidinone; Baylis Hillman; Indium; Nitroalkanoate; SnCl2 2H2O

Indexed keywords

ACETIC ACID DERIVATIVE; ALKANOIC ACID; CARBENE; CARBONYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; ETHANE; HYDROCHLORIC ACID; INDIUM; INDOLE DERIVATIVE; NITRO DERIVATIVE; OXIME DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PYRROLIDINE DERIVATIVE; TIN DERIVATIVE; VINYL DERIVATIVE;

ARTICLE; BAYLIS HILLMAN REACTION; CIS TRANS ISOMERISM; CYCLIZATION; PRIORITY JOURNAL; QUANTUM YIELD; REACTION ANALYSIS; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

EID: 33748413757     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.08.045     Document Type: Article

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