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(2S,3S)-2-[(TERT.-BUTOXYCARBONYL)-AMINO]-3-METHYL-PENT-4-ENOIC-ACID

Compound with spectra: 1 NMR

(2S,3S)-2-[(TERT.-BUTOXYCARBONYL)-AMINO]-3-METHYL-PENT-4-ENOIC-ACID
SpectraBase Compound ID D7S72GLAcsM
InChI InChI=1S/C11H19NO4/c1-6-7(2)8(9(13)14)12-10(15)16-11(3,4)5/h6-8H,1H2,2-5H3,(H,12,15)(H,13,14)/t7-,8-/m0/s1
InChIKey AVIBDPLENQNIOH-YUMQZZPRSA-N
Mol Weight 229.28 g/mol
Molecular Formula C11H19NO4
Exact Mass 229.131408 g/mol
Enantiomer InChIKey AVIBDPLENQNIOH-HTQZYQBOSA-N

View Spectrum of (2S,3S)-2-[(TERT.-BUTOXYCARBONYL)-AMINO]-3-METHYL-PENT-4-ENOIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2S,3R)-2-((tert-Butoxycarbonyl)amino)-3-methylpent-4-enoic acid
2-[N-[(TERT.-BUTYLOXY)-CARBONYL]-AMINO]-4-FLUORO-4-PENTENOIC-ACID;MAJOR-ROTAMER+MINOR-ROTAMER
(2S)-2-(tert-butoxycarbonylamino)hexa-4,5-dienoic acid methyl ester
N-(tert-Butoxycarbonyl)-D-aspartic acid
N-Boc-L-aspartic acid
L-2-(carboxyamino)-4-hydroxybutric acid, N-tert-butyl ester, compound with dicyclohexylamine(1.1)
Boc-Gln-OH
N-(tert-Butoxycarbonyl)-D-glutamic acid
Nsquare-carboxy-L-asparagine, Nsquare-tert-butyl ester
Boc-Asn-OH
Title Journal or Book Year
Stereoselective Synthesis of Proline-Derived Dipeptide Scaffolds (ProM-3 and ProM-7) Rigidified in a PPII Helix Conformation European Journal of Organic Chemistry 2014
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