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METHYL-(2R,2'S)-2-AZIDO-3-[3-(1-BENZYL-1H-IMIDAZOL-4-YL)-2-(TERT.-BUTOXYCARBONYLAMINO)-PROPANOYLTHIO]-PROPIONATE

Compound with spectra: 1 NMR

METHYL-(2R,2'S)-2-AZIDO-3-[3-(1-BENZYL-1H-IMIDAZOL-4-YL)-2-(TERT.-BUTOXYCARBONYLAMINO)-PROPANOYLTHIO]-PROPIONATE
SpectraBase Compound ID IyRwNJ17A6O
InChI InChI=1S/C22H28N6O5S/c1-22(2,3)33-21(31)25-17(20(30)34-13-18(26-27-23)19(29)32-4)10-16-12-28(14-24-16)11-15-8-6-5-7-9-15/h5-9,12,14,17-18H,10-11,13H2,1-4H3,(H,25,31)/t17-,18-/m0/s1
InChIKey HLERGOONDGCRRT-ROUUACIJSA-N
Mol Weight 488.56 g/mol
Molecular Formula C22H28N6O5S
Exact Mass 488.184189 g/mol
Enantiomer InChIKey HLERGOONDGCRRT-QZTJIDSGSA-N

View Spectrum of METHYL-(2R,2'S)-2-AZIDO-3-[3-(1-BENZYL-1H-IMIDAZOL-4-YL)-2-(TERT.-BUTOXYCARBONYLAMINO)-PROPANOYLTHIO]-PROPIONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
T-Butoxycarbonyl-histidyl(T-butoxycarbonyl)-glycine benzyl ester
1-BENZOYL-3-ISOBUTYL-3-[1-(1'-BENZYL-4'-IMIDAZOLYL)-3-HYDROXYPROP-2(S)-YL]-UREA
T-Butoxycarbonyl-histidyl(T-butoxycarbonyl)-T-glycine benzyl ester
(2S-(R*,R*))-N-(2-(((1,1-DIMETHYL)-ETHOXYCARBONYL)-AMINO)-1-OX-3-(3-THIENYL)-PROPYL)-HISTIDINE_METHYLESTER
N-(N-((1,1-DIMETHYL)-ETHOXYCARBONYL)-L-PHENYLALANYL)-L-2-METHYLHISTIDINE-METHYLESTER,N-(N-((1,1-DIMETHYL)-ETHOXYCARBONYL)-L-PHENYLALANYL)-D-2
O,N-permethylated ac-ala-his
(2S)-N-(TERT.-BUTOXYCARBONYL)-PHENYLALANYL-BETA-ALANYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSYL-[ALPHA-METHYL-(2R)-ASPARTATE]-DIESTER;ROTAMER-#2
(2S)-N-(TERT.-BUTOXYCARBONYL)-PHENYLALANYL-BETA-ALANYL-[ALPHA-METHYL-(2R)-GLUTAMYL]-GAMMA-SARCOSYL-[ALPHA-METHYL-(2R)-ASPARTATE]-DIESTER;ROTAMER-#1
(2R*,3S*)-2-BROMO-3-FLUORO-3-(1-TRITYL-1H-IMIDAZOL-4-YL)-PROPANOIC-ACID-METHYLESTER
BOC-PHE-CYS((O)ME)-SER(TERT.-BUTYL)-O(TERT.-BUTYL)
Title Journal or Book Year
Unified Azoline and Azole Syntheses by Optimized Aza-Wittig Chemistry European Journal of Organic Chemistry 2013
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