Lewis acids as mild and effective catalysts for the synthesis of 3,5-bis[(hetero)arylidene]piperidin-4-ones

Helvetica Chimica Acta

Volumn 93, Issue 10, 2010, Pages 1990-1999

  Leonova, Evgeniya ^a   Makarov, Mihail ^a   Klemenkova, Zinaida ^a   Odinets, Irina ^a  

^a A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

Author keywords

Aldol crotonic condensation reactions; Lewis acids; Piperidin 4 ones, 3,5 bis(heteroarylidene)

Indexed keywords

ALDOL-CROTONIC CONDENSATION REACTIONS; ALKYL SUBSTITUENT; AROMATIC ALDEHYDE; AROMATIC GROUP; CATALYTIC SYSTEM; COMPARATIVE STUDIES; DEPROTECTION; HIGH YIELD; LABILE GROUPS; LEWIS ACID; PIPERIDIN-4-ONES, 3,5-BIS(HETEROARYLIDENE)-; TERTIARY AMINE;

ACIDS; ALDEHYDES; ALKYLATION; AROMATIC COMPOUNDS; CATALYSTS; CONDENSATION; REACTION RATES; SYNTHESIS (CHEMICAL);

CONDENSATION REACTIONS;

1 METHYL 3,5 BIS(4 NITROBENZYLIDENE) 4 OXOPIPERIDINIUM TETRAFLUOROBORATE; 1 METHYL 3,5 BIS(PYRIDIN 2 YLMETHYLIDENE)PIPERIDIN 4 ONE; 1 METHYL 3,5 BIS(PYRIDIN 3 YLMETHYLIDENE)PIPERIDIN 4 ONE; 1 METHYL 3,5 BIS(THIOPHEN 2 YLMETHYLIDENE)PIPERIDIN 4 ONE; 1 METHYL 4 OXO 3,5 BIS(PYRIDIN 3 YLMETHYLIDENE)PIPERIDINIUM TETRAFLUOROBORATE; 3,5 BIS(4 CYANOBENZYLIDENE) 1 METHYL 4 OXOPIPERIDINIUM TETRAFLUOROBORATE; 3,5 BIS(4 CYANOBENZYLIDENE) 4 OXOPIPERIDINIUM TETRAFLUOROBORATE; 3,5 BIS(4 FLUOROBENZYLIDENE) 1 METHYL 4 OXOPIPERIDINIUM TETRAFLUOROBORATE; 3,5 BIS(4 FLUOROBENZYLIDENE) 4 OXOPIPERIDINIUM TETRAFLUOROBORATE; 3,5 BIS[4 (DIMETHYLAMINO)BENZYLIDENE] 1 METHYLPIPERIDIN 4 ONE; 4,4' [(4 OXOPIPERIDINE 3,5 DIYLIDENE)DI(METHYLIDENE)]DIBENZAMIDE; 4,4'[(1 METHYL 4 OXOPIPERIDINE 3,5 DIYLIDENE)DIMETHYLYLIDENE]DIBENZONITRILE; ACID; ALDEHYDE; ALKYL GROUP; BASE; BROMIDE; CROTONIC ACID DERIVATIVE; LEWIS ACID; LITHIUM CHLORIDE; MAGNESIUM BROMIDE; PIPERIDONE DERIVATIVE; TERTIARY AMINE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; ATOM; CATALYST; COMPARATIVE STUDY; DEPROTECTION REACTION; DRUG SYNTHESIS; PRIORITY JOURNAL; QUANTUM YIELD;

EID: 78349269064     PISSN: 0018019X     EISSN: 15222675     Source Type: Journal    
DOI: 10.1002/hlca.201000005     Document Type: Article

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