Synthesis of spiro bis-indanes via domino Stetter-aldol-Michael and Stetter-aldol-aldol reactions: Scope and limitations

Synthesis

Volumn , Issue 12, 2011, Pages 1896-1904

  Sánchez Larios, Eduardo ^a   Holmes, Janice M ^a   Daschner, Crystal L ^a   Gravel, Michel ^a  

^a UNIVERSITY OF SASKATCHEWAN   (Canada)

Author keywords

aldol; domino reactions; Michael; NHC; organocatalysis; Stetter; umpolung

Indexed keywords

ALDOL; DOMINO REACTIONS; MICHAEL; NHC; ORGANOCATALYSIS; STETTER; UMPOLUNG;

CARBON INORGANIC COMPOUNDS; CATALYSIS; ORGANIC COMPOUNDS; REACTION KINETICS;

SYNTHESIS (CHEMICAL);

2' BENZOYL 1 HYDROXY 3' (2 OXO 2 PHENYLETHYL) 2',3' DIHYDRO 1,2' SPIROBI[INDEN] 3(1H) ONE; 2' BENZOYL 1,3' DIHYDROXY 3' PHENYL 2',3' DIHYDRO 1,2' SPIROBI[INDEN] 3(1H) ONE; 2,2' (3,4,7,8 TETRAHYDRODIBENZO[8]ANNULENE)BIS(1 PHENYLPROPAN 1 ONE); 2,2' (3,4,7,8 TETRAHYDRODIBENZO[8]ANNULENE)DIACETONITRILE; 2,2' BIS(PHENYLSULFONYLMETHYL)(3,4,7,8 TETRAHYDRODIBENZO[8]ANNULENE); DIETHYL 2,2' (3,4,7,8 TETRAHYDRODIBENZO[8]ANNULENE)DIACETATE; INDAN DERIVATIVE; REL 2' BENZOYL 1 HYDROXY 1,2' SPIRO[INDEN] 3(1H) ONE; REL 2' BENZOYL 3 (2 OXO 2 PHENYLETHYL) 1,2' SPIRO[INDEN] 1(3H) ONE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIMERIZATION; DOMINO STETTER ALDOL MICHAEL REACTION; ELECTROPHILICITY; MICHAEL ADDITION; PROCESS OPTIMIZATION; STETTER ALDOL ALDOL REACTION; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 79958164776     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260031     Document Type: Article

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