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N-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-HYDROXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER

Compound with spectra: 2 NMR

N-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-HYDROXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
SpectraBase Compound ID CbaWJClmEN7
InChI InChI=1S/C18H26N2O4/c1-18(2,3)24-17(23)19-13-16(22)20(11-7-8-12-21)14-15-9-5-4-6-10-15/h4-10,21H,11-14H2,1-3H3,(H,19,23)/b8-7+
InChIKey POIHOTRJXRRANS-BQYQJAHWSA-N
Mol Weight 334.42 g/mol
Molecular Formula C18H26N2O4
Exact Mass 334.189257 g/mol

View Spectrum of N-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-HYDROXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER

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-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-HYDROXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • N-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-HYDROXY-(2E)-BUTEN-1-YL]]-AMIDE;MINOR-ROTAMER
N-TRIFLUOROACETYL-GLYCYL-[N-BENZYL-N-[4-HYDROXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
N-TERT.-BUTYLOXYCARBONYL-BETA-ALANYL-[N-BENZYL-N-[4-HYDROXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
N-BENZYL-4-[TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]-TRIFLUORACETAMIDE;MAJOR-ROTAMER
(E)-Ethyl 4-(N-Benzyl-N-tert-butyloxycarbonylamino)but-2-enoate
(S)-1-[(N-Benzyl-N-tert-butoxycarbonyl)amino]hex-2-en-4-ol
1-Benzyl-4-methylpiperazine-2,5-dione
N,N-Dibenzyl-2-[(benzyl)(but-3-enyl)amino]acetamide
Carbamic acid, [2-[methyl(phenylmethyl)amino]-2-oxoethylidene]bis-, dimethyl ester
1,4-Dibenzyl-1,4-diazepane-5,7-dione
N-BENZYL-6-METHYL-3,6-DIHYDRO-2-PYRIDONE;MAJOR
Title Journal or Book Year
Synthesis of α-Amino-γ-lactams through Pd-Catalzed Intramolecular Allylic Alkylation of Sarcosine Allyl Amides European Journal of Organic Chemistry 2014
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