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METHYL-(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROPYL]-4-HYDROXYPROLINATE;CONFORMER-CT

Compound with spectra: 2 NMR

METHYL-(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROPYL]-4-HYDROXYPROLINATE;CONFORMER-CT
SpectraBase Compound ID 4QdNJdh0LsI
InChI InChI=1S/C16H26N2O6/c1-16(2,3)24-15(22)17-7-5-6-11(17)13(20)18-9-10(19)8-12(18)14(21)23-4/h10-12,19H,5-9H2,1-4H3/t10?,11-,12-/m0/s1
InChIKey OZBMKNMWXIFBFW-RAMGSTBQSA-N
Mol Weight 342.39 g/mol
Molecular Formula C16H26N2O6
Exact Mass 342.179087 g/mol
Enantiomer InChIKey OZBMKNMWXIFBFW-PQDIPPBSSA-N

View Spectrum of METHYL-(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROPYL]-4-HYDROXYPROLINATE;CONFORMER-CT

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

View Spectrum of METHYL-(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROPYL]-4-HYDROXYPROLINATE;CONFORMER-CT

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • METHYL-(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROPYL]-4-HYDROXYPROLINATE;CONFORMER-TT
(2S,4R)-N-[(2S)-N-(TERT.-BUTOXYCARBONYL)-PROLYL]-4-HYDROXYPROLINE-METHYLAMIDE
tert-Butyl 2-[(2-([2-(methoxycarbonyl)-1-pyrrolidinyl]carbonyl)-1-pyrrolidinyl)carbonyl]-1-pyrrolidinecarboxylate
TERT-BUTYLOXYCARBONYL-PROLIN-PROLIN-GLYCIN-ALANIN-GLYCIN-O-BENZYLPEPTIDE
Leucyi-prolyl-(S-farnesyl)cysteine methyl ester
METHYL-(2S)-(3-BUTENYL-[[(2S)-1-(2,2,2-TRIFLUOROACETYL)-TETRAHYDRO-1H-PYRROL-2-YL]-CARBONYL]-AMINO)-3-PHENYLPROPANOATE
METHYL-(2R)-(3-BUTENYL-[[(2S)-1-(2,2,2-TRIFLUOROACETYL)-TETRAHYDRO-1H-PYRROL-2-YL]-CARBONYL]-AMINO)-3-PHENYLPROPANOATE
Artifact of roasted food AC @
BENZYLOXYCARBONYL-GLYCIN-PROLIN-PROLIN-GLYCIN-ALANIN-GLYCIN-O-BENZYLPEPTIDE
(S)-tert-Butyl 2-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-ylcarbamoyl]pyrrolidine-1-carboxylate
(1S,3R,4R)-N-tert-Butoxycarbonyl-3-[N-(trans-(2R,5R)-2,5-dimethyl)pyrrolidinyl]carbonyl-2-azabicyclo[2.2.1]heptane
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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