Enantioselective synthesis of (+)- l -733,060 and (+)-CP-99,994: Application of an ireland-claisen rearrangement/michael addition domino sequence

Synlett

Volumn , Issue 3, 2010, Pages 387-390

  Garrido, Narciso M ^a   García, Mercedes ^a   Sánchez, M Rosa ^a   Díez, David ^a   Urones, Julio G ^a  

^a UNIVERSITY OF SALAMANCA   (Spain)

Author keywords

amino acids; Asymmetric synthesis; Chiral auxiliaries; Chiral piperidines; Domino reactions

Indexed keywords

3 (2 METHOXYBENZYLAMINO) 2 PHENYLPIPERIDINE; 3 [3,5 BIS(TRIFLUOROMETHYL)BENZYLOXY] 2 PHENYLPIPERIDINE; HYDROXYL GROUP; PIPERIDONE DERIVATIVE;

ARTICLE; ASYMMETRIC SYNTHESIS; BAYLIS HILLMAN REACTION; CHEMICAL REACTION; CLAISEN REARRANGEMENT; DRUG SYNTHESIS; ENANTIOSELECTIVITY; HYDROGENOLYSIS; IRELAND CLAISEN REARRANGEMENT; LACTAMIZATION; MICHAEL ADDITION; ONE POT SYNTHESIS; QUANTUM YIELD; STEREOCHEMISTRY;

EID: 76249096743     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1219200     Document Type: Article

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