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N-TERT.-BUTYLOXYCARBONYL-SARCOSYL-[N-[4-ETHOXYCARBONYLOXY-(2E)-BUTEN-1-YL]-N-(2-TETRAHYDROPYRAN-2-YL-OXY-ETHYL)]-AMIDE;MAJOR-ROTAMER

Compound with spectra: 2 NMR

N-TERT.-BUTYLOXYCARBONYL-SARCOSYL-[N-[4-ETHOXYCARBONYLOXY-(2E)-BUTEN-1-YL]-N-(2-TETRAHYDROPYRAN-2-YL-OXY-ETHYL)]-AMIDE;MAJOR-ROTAMER
SpectraBase Compound ID 58daenzwG8G
InChI InChI=1S/C22H38N2O8/c1-6-28-21(27)31-15-10-8-12-24(13-16-30-19-11-7-9-14-29-19)18(25)17-23(5)20(26)32-22(2,3)4/h8,10,19H,6-7,9,11-17H2,1-5H3/b10-8+
InChIKey AOFAPEDZGRGQIA-CSKARUKUSA-N
Mol Weight 458.6 g/mol
Molecular Formula C22H38N2O8
Exact Mass 458.262816 g/mol

View Spectrum of N-TERT.-BUTYLOXYCARBONYL-SARCOSYL-[N-[4-ETHOXYCARBONYLOXY-(2E)-BUTEN-1-YL]-N-(2-TETRAHYDROPYRAN-2-YL-OXY-ETHYL)]-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-SARCOSYL-[N-[4-ETHOXYCARBONYLOXY-(2E)-BUTEN-1-YL]-N-(2-TETRAHYDROPYRAN-2-YL-OXY-ETHYL)]-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-SARCOSYL-[N-[4-ETHOXYCARBONYLOXY-(2E)-BUTEN-1-YL]-N-(2-TETRAHYDROPYRAN-2-YL-OXY-ETHYL)]-AMIDE;MINOR-ROTAMER
cis-T-Butoxycarbonyl-sarcosyl-N-methyl-L-valine methyl ester
QNLMVXZHCWBETC-LBPRGKRZSA-N
t-Butyl 3(R)-[(tetrahydro-2H-pyran-2'-yloxy)methyl]-3,6-dihydro-2H-pyridine-1-carboxylate
METHYL-N(2.1)-[(BENZYLOXY)-CARBONYL]-L-VALYLSARCOSINATE
2-Oxo-4-pent-4-enyloxy-2,5-dihydropyrrol-1-carboxylic acid tert-Butyl Ester
Tert-Butyl Allyl[(2S,3S)-3-(methoxymethoxy)pent-4-en-2-yl]carbamate
(2R)-2-methyl-4-(phenylmethyl)-1-piperazinecarboxylic acid tert-butyl ester
(2S)-2-methyl-4-(phenylmethyl)-1-piperazinecarboxylic acid tert-butyl ester
Methyl (2RS)-2-(N-t-butoxycarbonyl-L-valyl)amino-2-methoxyacetate
2-[[2-(tert-butoxycarbonylamino)-3-phenyl-propanoyl]amino]acetic acid [(E)-but-2-enyl] ester
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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