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(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROLYL]-4-HYDROXYPROLINE-METHYLAMIDE

Compound with spectra: 3 NMR

(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROLYL]-4-HYDROXYPROLINE-METHYLAMIDE
SpectraBase Compound ID 6MkcQaAPXFf
InChI InChI=1S/C16H27N3O5/c1-16(2,3)24-15(23)18-7-5-6-11(18)14(22)19-9-10(20)8-12(19)13(21)17-4/h10-12,20H,5-9H2,1-4H3,(H,17,21)/t10?,11-,12-/m0/s1
InChIKey DSJGREBSIWAUNK-RAMGSTBQSA-N
Mol Weight 341.41 g/mol
Molecular Formula C16H27N3O5
Exact Mass 341.195071 g/mol
Enantiomer InChIKey DSJGREBSIWAUNK-PQDIPPBSSA-N

View Spectrum of (2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROLYL]-4-HYDROXYPROLINE-METHYLAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROLYL]-4-HYDROXYPROLINE-METHYLAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROLYL]-4-HYDROXYPROLINE-METHYLAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
TERT-BUTYLOXYCARBONYL-PROLIN-PROLIN-GLYCIN-ALANIN-GLYCIN-O-BENZYLPEPTIDE
ETHYL-N-[(N-TERT.-BUTYLOXYCARBONYL)-L-PROL-2-YL]-L-THIAZOLIDINE-4-CARBOXYLATE
BENZYLOXYCARBONYL-GLYCIN-PROLIN-PROLIN-GLYCIN-ALANIN-GLYCIN-O-BENZYLPEPTIDE
METHYL-(2R)-(3-BUTENYL-[[(2S)-1-(2,2,2-TRIFLUOROACETYL)-TETRAHYDRO-1H-PYRROL-2-YL]-CARBONYL]-AMINO)-3-PHENYLPROPANOATE
METHYL-(2S)-(3-BUTENYL-[[(2S)-1-(2,2,2-TRIFLUOROACETYL)-TETRAHYDRO-1H-PYRROL-2-YL]-CARBONYL]-AMINO)-3-PHENYLPROPANOATE
(S)-tert-Butyl 2-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-ylcarbamoyl]pyrrolidine-1-carboxylate
N-TERT.-BUTYLOXYCARBONYL-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLYL-S-HEXADECYL-L-CYSTEINE-METHYLESTER
Desmethyl-destruxin B - methyl ester
MKN-349A
(2R)-2-(N-Benzyloxycarbonyl)-N-(2,2-diethoxyethyl)amino)pent-4-enoic acid [(2S)-tert-butyldimethylsiloxymethylpyrrolidinyl]amide
Title Journal or Book Year
Design, construction and properties of peptide N-terminal cap templates devised to initiate α-helices. Part 2.† Caps derived from N-[(2S )-2-chloropropionyl]-(2S )-Pro-(2S )-Pro-(2S,4S )-4-thioPro-OMe Journal of the Chemical Society, Perkin Transactions 1 1998
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