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N-[N-(TERT.-BUTOXYCARBONYL)-N-METHYL-LEUCYL-(ALPHA,BETA-DIDEHYDRO)-ALANYL]-O-TERT.-BUTYL-L-ALANIN;DIASTEREOMER-1

Compound with spectra: 2 NMR

N-[N-(TERT.-BUTOXYCARBONYL)-N-METHYL-LEUCYL-(ALPHA,BETA-DIDEHYDRO)-ALANYL]-O-TERT.-BUTYL-L-ALANIN;DIASTEREOMER-1
SpectraBase Compound ID L2ijllNPdnQ
InChI InChI=1S/C22H39N3O6/c1-13(2)12-16(25(11)20(29)31-22(8,9)10)18(27)23-14(3)17(26)24-15(4)19(28)30-21(5,6)7/h13,15-16H,3,12H2,1-2,4-11H3,(H,23,27)(H,24,26)/t15-,16-/m0/s1
InChIKey KHOPNKLVPYBEBH-HOTGVXAUSA-N
Mol Weight 441.6 g/mol
Molecular Formula C22H39N3O6
Exact Mass 441.283886 g/mol
Enantiomer InChIKey KHOPNKLVPYBEBH-HZPDHXFCSA-N

View Spectrum of N-[N-(TERT.-BUTOXYCARBONYL)-N-METHYL-LEUCYL-(ALPHA,BETA-DIDEHYDRO)-ALANYL]-O-TERT.-BUTYL-L-ALANIN;DIASTEREOMER-1

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

View Spectrum of N-[N-(TERT.-BUTOXYCARBONYL)-N-METHYL-LEUCYL-(ALPHA,BETA-DIDEHYDRO)-ALANYL]-O-TERT.-BUTYL-L-ALANIN;DIASTEREOMER-1

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • N-[N-(TERT.-BUTOXYCARBONYL)-N-METHYL-LEUCYL-(ALPHA,BETA-DIDEHYDRO)-ALANYL]-O-TERT.-BUTYL-L-ALANIN;DIASTEREOMER-2
2-((1-(1-(1-hydroxy-2-methylpropyl)carbonylamino)4-(4-methoxyphenyl)butyl)carbonylamino)ethenyl)carbonylamino)propanoic acid methyl ester
TERT-BUTYLOXYCARBONYL-PROLIN-GLYCIN-ALANIN-GLYCIN-O-BENZYL PEPTIDE
N-tert-butyloxycarbonyl-L-prolyl-D,L-.alphas.-methoxyglycine methyl ester
cis-N-Benzyloxycarbonyl-prolyl-alanyl-glycine
tert-butyl (S)-2-((2-oxo-2-(p-tolyl)ethyl)carbamoyl)piperidine-1-carboxylate
Methyl N-(Benzyloxycarbonyl)-1-prolyl-1-serinate
BOC-PHE-CYS(ME)-ALA-OALL
N-[N-ACETYL-L-PHENYLALANYL-(BETA-O-ACETYL)-L-SERYL]-O-TERT.-BUTYL-L-ALANIN
BENZYLOXYCARBONYL-VALINE-GLYCINE-(TERT-BUTYLOXYCARBONYL)LYSINE-(TERT-BUTYLOXYCARBONYL)LYSINE TETRAPEPTIDE
N-TERT.-BUTOXYCARBONYL-L-THREONYL-L-LEUCYL-L-SERYL-L-ALANINE;BOC-THR-LEU-SER-ALA-OH
Title Journal or Book Year
Dehydroalanine-Containing Peptides by AcOH-Elimination fromO-Acetylserine Residuces with DBU/LiClO4 in Tetrahydrofuran Helvetica Chimica Acta 1993
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