Five- and six-membered nickelacyclic carboxylates as reagents for the facile synthesis of δ-ketocarboxylic acids, isocoumarins, and 1,3-dicarbonyl derivatives of benzoic acid

Synthesis

Volumn , Issue 16, 2006, Pages 2697-2706

  Langer, Jens ^a   Gärtner, Martin ^a   Görls, Helmar ^a   Walther, Dirk ^a  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

Cross coupling; Heterocycles; Metallacycles; Nickel; Organometallic reagents

Indexed keywords

CARBOXYLIC ACIDS; KETONES; NICKEL; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

CROSS COUPLING; HETEROCYCLES; METALLACYCLES; ORGANOMETALLIC REAGENTS;

ESTERS;

1,3 DICARBONYL BENZOIC ACID DERIVATIVE; 2 (1 METHYL 2 OXO 2 PHENYLETHYL)BENZOIC ACID; 2 (2 OXOTETRAHYDROFURAN 3 YL)BENZOIC ACID; 2 [2 (2 NAPHTHYL) 2 OXOETHYL]BENZOIC ACID; 2 [2 (2,4 DICHLOROPHENYL) 2 OXOETHYL]BENZOIC ACID; 2 [2 (4 BROMOPHENYL) 2 OXOETHYL)BENZOIC ACID; 2 [2 (4 CYANOPHENYL) 2 OXOETHYL]BENZOIC ACID; 2 [4,7,7 TRIMETHYL 3 OXOBICYCLO[2.2.1]HEPT 2 YL]BENZOIC ACID; 2 ETHYL 3 (2 OXOTETRAHYDROFURAN 3 YL)PENT 2 ENOIC ACID; 3 (2 NAPHTHYL)ISOCOUMARIN; 3 (2,4 DICHLOROPHENYL)ISOCOUMARIN; 3 (4 BROMOPHENYL)ISOCOUMARIN; 3 HYDROXY 3,4 DIMETHYL 3,4 DIHYDROISOCOUMARIN; 3,4 DIETHYL 6 HYDROXY 5,6 DIMETHYL 5,6 DIHYDRO 2H PYRAN 2 ONE; 3,4 DIETHYL 6 HYDROXY 6 (2 NAPHTHYL) 5,6 DIHYDRO 2H PYRAN 2 ONE; 5,6 DIETHYL 2 HYDROXY 1,11,11 TRIMETHYL 3 OXA TRICYCLO[6.2.1.0 2.7 ]UNDEC 5 EN 4 ONE; 6 (2,4 DICHLOROPHENYL) 3,4 DIETHYL 6 HYDROXY 5,6 DIHYDRO 2H PYRAN 2 ONE; 6 (4 BROMOPHENYL) 3,4 DIETHYL 6 HYDROXY 5,6 DIHYDRO 2H PYRAN 2 ONE; 6 (4 CYANOPHENYL) 3,4 DIETHYL 6 HYDROXY 5,6 DIHYDRO 2H PYRAN 2 ONE; BENZOIC ACID DERIVATIVE; CARBONYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; DELTA KETOCARBOXYLIC ACID DERIVATIVE; FURAN DERIVATIVE; ISOCOUMARIN DERIVATIVE; KETONE DERIVATIVE; NICKEL; NICKELACYCLIC CARBOXYLATE DERIVATIVE; ORGANOMETALLIC COMPOUND; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DEHYDRATION; SYNTHESIS; X RAY DIFFRACTION;

EID: 33748286700     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-942507     Document Type: Article

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