A convenient synthesis of chiral 1,2,4-oxadiazoles from N-protected (α-aminoacyl)benzotriazoles

Arkivoc

Volumn 2005, Issue 7, 2005, Pages 36-55

  Katritzky, Alan R ^a   Shestopalov, Aleksandr A ^a   Suzuki, Kazuyuki ^a  

^a University of Florida ^*  (United States)

Author keywords

Benzotriazole methodology; Chiral 1,2,4 oxadiazole; N acylbenzotriazole; N aminoacylbenzotriazole

Indexed keywords

(9H FLUOREN 9 YL)METHYL 1 (3 BENZYL 1,2,4 OXADIAZOL 5 YL) 3 (METHYLTHIO)PROPYLCARBAMIC ACID; (9H FLUOREN 9 YL)METHYL 2 (1H INDOL 3 YL) 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]ETHYLCARBAMIC ACID; (9H FLUOREN 9 YL)METHYL 2 PHENYL 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]ETHYLCARBAMIC ACID; (9H FLUOREN 9 YL)METHYL 3 (METHYLTHIO) 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]PROPYLCARBAMIC ACID; AMINO ACID DERIVATIVE; BENZOTRIAZOLE DERIVATIVE; BENZYL 1 (3 BENZYL 1,2,4 OXADIAZOL 5 YL) 2 PHENYLETHYLCARBAMIC ACID; BENZYL 1 (3 BENZYL 1,2,4 OXADIAZOL 5 YL) 3 (METHYLTHIO)PROPYLCARBAMIC ACID; BENZYL 1 (3 BENZYL 1,2,4 OXADIAZOL 5 YL)ETHYLCARBAMIC ACID; BENZYL 1 (3 PYRIDIN 4 YL) 1,2,4 OXADIAZOL 5 YLETHYLCARBAMIC ACID; BENZYL 1 [2 METHYL 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]PROPYLAMINO] 1 OXOPROPAN 2 YLCARBAMIC ACID; BENZYL 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]ETHYLCARBAMIC ACID; BENZYL 1 OXO 1 [2 PHENYL 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]ETHYLAMINO]PROPAN 2 YLCARBAMIC ACID; BENZYL 1 OXO 3 PHENYL 1 [1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]ETHYLAMINO]PROPAN 2 YLCARBAMIC ACID; BENZYL 2 METHYL 1 (3 PYRIDIN 4 YL) 1,2,4 OXADIAZOL 5 YLPROPYLCARBAMIC ACID; BENZYL 2 METHYL 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]PROPYLCARBAMIC ACID; BENZYL 2 PHENYL 1 (3 PYRIDIN 4 YL) 1,2,4 OXADIAZOL 5 YLETHYLCARBAMIC ACID; BENZYL 2 PHENYL 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]ETHYLCARBAMIC ACID; BENZYL 3 (METHYLTHIO) 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]PROPYLCARBAMIC ACID; BENZYL 4 AMINO 4 OXO 1 [3 (4 TOLYL) 1,2,4 OXADIAZOL 5 YL]BUTYLCARBAMIC ACID; N ACYLAMINO ACID; NITROGEN DERIVATIVE; OXADIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHIRALITY; CYCLIZATION; DECOMPOSITION; ENANTIOMER; ENERGY YIELD; HEATING; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; ISOMERISM; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; SYNTHESIS;

EID: 15544384919     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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