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N-TERT.-BUTYLOXYCARBONYL-SARCOSYL-[N-[4-HYDROXY-(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-HYDROXY-(2E)-BUTEN-1-YL]-N-(2-TETRAHYDROPYRAN-2-YL-OXY-ETHYL)]-AMIDE;MAJOR-ROTAMER
SpectraBase Compound ID YKtQ7mAUbd
InChI InChI=1S/2C19H34N2O6/c2*1-19(2,3)27-18(24)20(4)15-16(23)21(10-6-7-12-22)11-14-26-17-9-5-8-13-25-17/h2*6-7,17,22H,5,8-15H2,1-4H3/b2*7-6+
InChIKey BDQGVIPUORKYSJ-YIKKBJQVSA-N
Mol Weight 773.0 g/mol
Molecular Formula C38H68N4O12
Exact Mass 772.483374 g/mol

View Spectrum of N-TERT.-BUTYLOXYCARBONYL-SARCOSYL-[N-[4-HYDROXY-(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-HYDROXY-(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-HYDROXY-(2E)-BUTEN-1-YL]-N-(2-TETRAHYDROPYRAN-2-YL-OXY-ETHYL)]-AMIDE;MINOR-ROTAMER
N-(4-phenoxyphenyl)-N-(2-tetrahydropyran-2-yloxyethyl)acetamide
TRANS-N-TERT.-BUTYLOXYCARBONYL-GLYCYLPROLINE
2-Oxo-4-pent-4-enyloxy-2,5-dihydropyrrol-1-carboxylic acid tert-Butyl Ester
N,N'-Di-tert-Butoxycarbonyl-1,5-diaza-3-isopropyliminocycloheptane
N,N-BIS-(TERT.-BUTOXYCARBONYL)-1,1-DIDEUTERIO-4-(TETRAHYDROPYRAN-2-YLOXY)-BUTYLAMINE
1-Piperazinecarboxylic acid, 4-ethyl-2,3-dioxo-, ethyl ester
N(2.1)-[(BENZYLOXY)-CARBONYL]-L-VALYLSARCOSINE
4-But-3-enylamino-2-oxo-2,5-dihydropyrrol-1-carboxylic acid tert-Butyl ester
N,N'-Di-tert-Butoxycarbonyl-1,5-diaza-3-ethoxyiminocycloheptane
VRELSIWZPREYLQ-NSHDSACASA-N
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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