Convenient one-pot two-step synthesis of 1,3-thiazoles via organocatalyzed epoxidation of nitroolefins

Synthesis (Germany)

Volumn 44, Issue 22, 2012, Pages 3441-3446

  Wei, Shengwei ^a   Weiß, Katharina M ^a   Tsogoeva, Svetlana B ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

DBU; epoxidation; one pot reaction; organocatalysis; thiazole

Indexed keywords

DBU; HETEROCYCLES; NITROOLEFINS; ONE POT; ONE-POT REACTION; ORGANOCATALYSIS; ORGANOCATALYTIC; THIAZOLE; THIOAMIDES; TWO-STEP SYNTHESIS;

CHEMISTRY; EPOXIDATION; SPEECH SYNTHESIS;

REACTION KINETICS;

2 (4 BUTYLPHENYL) 4 METHYL 5 (NAPHTHALEN 2 YL)THIAZOLE; 2 (4 CHLOROPHENYL) 4 METHYL 5 (NAPHTHALEN 2 YL)THIAZOLE; 2 (4 CHLOROPHENYL) 4 METHYL 5 PHENYLTHIAZOLE; 2 (4 CHLOROPHENYL) 5 (2 METHOXYPHENYL) 4 METHYLTHIAZOLE; 2 (4 METHOXYPHENYL) 4 METHYL 5 (NAPHTHALEN 2 YL)THIAZOLE; 2 (4 METHOXYPHENYL) 4 METHYL 5 PHENYLTHIAZOLE; 2 (4 TERT BUTYLPHENYL) 5 (2 METHOXYPHENYL) 4 METHYLTHIAZOLE; 2 (4 TERT BUTYLPHENYL) 5 (4 BROMOPHENYL) 4 METHYLTHIAZOLE; 2 (4 TERT BUTYLPHENYL) 5 (4 METHOXYPHENYL) 4 METHYLTHIAZOLE; 2 [4 (TERT BUTYL)PHENYL] 4 METHYL 5 PHENYLTHIAZOLE; 2 [4 (TERT BUTYL)PHENYL] 5 (4 CHLOROPHENYL) 4 METHYLTHIAZOLE; 2,5 BIS(4 CHLOROPHENYL) 4 METHYLTHIAZOLE; 4 METHYL 2,5 DIPHENYLTHIAZOLE; 4 METHYL 5 (NAPHTHALEN 2 YL) 2 PHENYLTHIAZOLE; 5 (2 METHOXYPHENYL) 4 METHYL 2 PHENYLTHIAZOLE; 5 (4 BROMOPHENYL) 2 (4 METHOXYPHENYL) 4 METHYLTHIAZOLE; 5 (4 BROMOPHENYL) 4 METHYL 2 PHENYLTHIAZOLE; 5 (4 CHLOROPHENYL) 2 (4 METHOXYPHENYL) 4 METHYLTHIAZOLE; 5 (4 CHLOROPHENYL) 4 METHYL 2 PHENYLTHIAZOLE; 5 (4 METHOXYPHENYL) 4 METHYL 2 PHENYLTHIAZOLE; ALKENE DERIVATIVE; NITROOLEFIN DERIVATIVE; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; EPOXIDATION; PROCESS OPTIMIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; PURIFICATION; ROOM TEMPERATURE; SYNTHESIS; THIN LAYER CHROMATOGRAPHY;

EID: 84868617425     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1291139     Document Type: Article

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