An efficient synthesis of new 2-aminomethyl-1,3,4-oxadiazoles from enantiomeric phenylglycine hydrazides

Tetrahedron

Volumn 65, Issue 6, 2009, Pages 1200-1206

  Kudelko, Agnieszka ^a   Zieliński, Wojciech ^a  

^a SILESIAN UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

2 Aminomethyl 1,3,4 oxadiazole; Enantiomers; Phenylglycine hydrazides; Protecting group; Racemization

Indexed keywords

1 (1,3,4 OXADIAZOL 2 YL) 1 PHENYLMETHYLAMMONIUM TRIFLUOROMETHANESULFONATE; 1 (5 ETHYL 1,3,4 OXADIAZOL 2 YL) 1 PHENYLMETHYLAMMONIUM TRIFLUOROMETHANESULFONATE; 1 (5 METHYL 1,3,4 OXADIAZOL 2 YL) 1 PHENYLMETHYLAMMONIUM TRIFLUOROMETHANESULFONATE; 1 (5 PHENYL 1,3,4 OXADIAZOL 2 YL) 1 PHENYLMETHYLAMMONIUM TRIFLUOROMETHANESULFONATE; 2 (1 AMINO 1 PHENYLMETHYL) 5 PHENYL 1,3,4 OXADIAZOLE HYDROCHLORIDE; 2 (1 N ACYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; 2 (1 N ACYLAMINO 1 PHENYLMETHYL) 5 PHENYL 1,3,4 OXADIAZOLE; 5 ETHYL 2 (1 N ACYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; 5 METHYL 2 (1 N ACYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; ACETIC ACID; ACETIC ACID DERIVATIVE; BENZOIC ACID DERIVATIVE; DEXTRO 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; DEXTRO 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 5 PHENYL 1,3,4 OXADIAZOLE; DEXTRO 5 ETHYL 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; DEXTRO 5 METHYL 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; FORMIC ACID DERIVATIVE; HYDRAZIDE DERIVATIVE; LEVO 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; LEVO 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 5 PHENYL 1,3,4 OXADIAZOLE; LEVO 5 ETHYL 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; LEVO 5 METHYL 2 (1 N TERT BUTOXYCARBONYLAMINO 1 PHENYLMETHYL) 1,3,4 OXADIAZOLE; OXADIAZOLE DERIVATIVE; PHENYLGLYCINE; PHENYLGLYCINE HYDRAZIDE HYDROCHLORIDE; PROPIONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DEPROTECTION REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 58149151068     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.11.096     Document Type: Article

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