One-pot synthesis of ureas from Boc-protected amines

Journal of Organic Chemistry

Volumn 79, Issue 10, 2014, Pages 4477-4483

  Spyropoulos, Constantinos ^a   Kokotos, Christoforos G ^a  

^a UNIVERSITY OF ATHENS   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; METABOLISM;

2-CHLOROPYRIDINE; HIGH YIELD; ONE-POT SYNTHESIS; SITU GENERATION;

UREA;

1 ALLYL 3 BENZYLUREA; 1 BENZYL 3 CYCLOHEXYLUREA; 1 BENZYL 3 PHENYLUREA; 1 BENZYL 4 METHYL 2 (3 BENZYLUREIDO)SUCCINATE; 1,3 DIBENZYLUREA; 4 (3 BENZYLUREIDO)BUTYL 4 (TRIFLUOROMETHYL)BENZOATE; ACID ANHYDRIDE; AMINE; BENZYL 1 [(1 METHOXY 1 OXO 3 PHENYLPROPAN 2 YL) CARBOMOYL]PYRROLIDINE 2 CARBOXYLATE; BENZYLPIPERIDINE 1 CARBOXAMIDE; ISOCYANATE; METHYL 2 (3 ALLYLUREIDO) 3 PHENYLPROPANOATE; METHYL 2 (3 BENZYLUREIDO) 3 METHYLBUTANOATE; METHYL 2 (3 BENZYLUREIDO) 3 PHENYLPROPANOATE; METHYL 2 (3 BENZYLUREIDO)ACETATE; METHYL 2 (3 CLYCLOHEXYLUREIDO) 3 PHENYLPROPANOATE; METHYL 2 (3 ISOPROPYLUREIDO) 3 PHENYLPROPANOATE; METHYL 2 (3 SEC BUTYLUREIDO) 3 PHENYLPROPANOATE; METHYL 2 (3 TERT BUTYLUREIDO) 3 PHENYLPROPANOATE; METHYL 2 (3,3 DIBENZYLUREIDO) 3 PHENYLPROPANOATE; METHYL 2 (MORPHOLINE 4 CARBOXAMIDO) 3 PHENYLPROPANOATE; METHYL 2 [3 (OCTADEC 9 EN 1 YL)UREIDO] 3 PHENYLPROPANOATE; METHYL 2 [3 [3,5 BIS(TRIFLUOROMETHYL)PHENYL]UREIDO] 3 PHENYLPROPANOATE; METHYL 3 PHENYL 2 (3 PHENYLUREIDO)PROPANOATE; METHYL 3 PHENYL 2 (3 PROPYLUREIDO)PROPANOATE; METHYL 3 PHENYL 2 (PIPERIDINE 1 CARBOXAMIDO) PROPANOATE; METHYL 3 PHENYL 2 [3 (1 PHENYLETHYL)UREIDO] PROPANOATE; METHYL 4 (3 BENZYLUREIDO)BUTANOATE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG; UREA DERIVATIVE; 2-CHLOROPYRIDINE; MESYLIC ACID DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID; UREA;

ARTICLE; CHIRAL CHROMATOGRAPHY; DIASTEREOISOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NUCLEOPHILICITY; ONE POT SYNTHESIS; REACTION TIME; ANALOGS AND DERIVATIVES; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

AMINES; MESYLATES; MOLECULAR STRUCTURE; PYRIDINES; UREA;

EID: 84900870288     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo500492x     Document Type: Article

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