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

Compound with spectra: 2 NMR

N-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
SpectraBase Compound ID LFHc9jv4RE0
InChI InChI=1S/C24H40N2O4Si/c1-23(2,3)30-22(28)25-18-21(27)26(19-20-14-10-9-11-15-20)16-12-13-17-29-31(7,8)24(4,5)6/h9-15H,16-19H2,1-8H3,(H,25,28)/b13-12+
InChIKey IPXFTXZOOSNHRG-OUKQBFOZSA-N
Mol Weight 448.7 g/mol
Molecular Formula C24H40N2O4Si
Exact Mass 448.275734 g/mol

View Spectrum of N-TERT.-BUTYLOXYCARBONYL-GLYCYL-[N-BENZYL-N-[4-TERT.-BUTYLDIMETHYLSILYLOXY-(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-TERT.-BUTYLDIMETHYLSILYLOXY-(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-TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]]-AMIDE;MINOR-ROTAMER
N-TRIFLUOROACETYL-GLYCYL-[N-BENZYL-N-[4-TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
N-TERT.-BUTYLOXYCARBONYL-BETA-ALANYL-[N-BENZYL-N-[4-TERT.-BUTYLDIMETHYLSILYLOXY-(2E)-BUTEN-1-YL]]-AMIDE;MAJOR-ROTAMER
(4S,5E)-7-[benzyl(tert-butoxycarbonyl)amino]-4-hydroxy-5-heptenyl pivalate
(E)-(S)-9-[(N-Benzyl-N-tert-butoxycarbonyl)amino]-6-hydroxy-7-nonenyl pivalate
(E)-(S)-8-[(N-Benzyl-N-tert-butoxycarbonyl)amino]-5-hydroxy-6-octenyl pivalate
butanoic acid, 4-[bis(phenylmethyl)amino]-4-oxo-, 2-(4-bromophenyl)-2-oxoethyl ester
(4s)-1-benzyl-4-((e)-styryl)-2-azetidinone
N-(2-Iodobenzyl)-N-benzylcyanoacetamide
(E)-3-(benzenesulfonyl)-N-(phenylmethyl)-N-prop-2-enyl-2-propenamide
(4R)-1-benzyl-4-(benzyloxymethyl)pyrrolidin-2-one
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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