Holzapfel-Meyers-Nicolaou modification of the Hantzsch thiazole synthesis

Synthesis

Volumn , Issue 22, 2007, Pages 3535-3541

  Merritt, Eleanor A ^a   Bagley, Mark C ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

Amino acids; Hantzsch; Heterocycles; Thiazoles

Indexed keywords

HANTZSCH; HETEROCYCLES; THIAZOLES; TRIFLUOROACETAMIDE DERIVATIVES;

BUILDING CODES; DERIVATIVES; ETHANOL; SODIUM COMPOUNDS; STEREOSELECTIVITY;

AMINO ACIDS;

3 (TERT BUTOXYCARBONYL) 2,2,5 TRIMETHYLOXAZOLIDINE 4 CARBOXYLIC ACID; ETHYL 2 [1 (TERT BUTOXYCARBONYLAMINO) 2 METHYLPROPYL]THIAZOLE 4 CARBOXYLATE; ETHYL 2 [1 [N (TERT BUTOXYCARBONYL) 2,2,2 TRIFLUOROACETAMIDO] 2 METHYLPROPYL]THIAZOLE 4 CARBOXYLATE; MICROCOCCIN P1; N TERT (BUTOXYCARBONYL)THIOVALINAMIDE; N TERT (BUTOXYCARBONYLA)VALINAMIDE; NOSTOCYCLAMIDE; PATELLAMIDE E; TERT BUTYL 4 [4 (ETHOXYCARBONYL)THIAZOL 2 YL] 2,2,5 TRIMETHYLOXAZOLIDINE 3 CARBOXYLATE; TERT BUTYL 4 CARBAMOTHIOYL 2,2,5 TRIMETHYLOXAZOLIDINE 3 CARBOXYLATE; TERT BUTYL 4 CARBAMOYL 2,2,5 TRIMETHYLOXAZOLIDINE 3 CARBOXYLATE; TERT BUTYL 4 CYANO 2,2,5 TRIMETHYLOXAZOLIDINE 3 CARBOXYLATE; THIAZOLE DERIVATIVE; THIOSTREPTON; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; POLYMERIZATION; RACEMIZATION; SOLVOLYSIS;

EID: 36749038293     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-990851     Document Type: Article

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