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BIS-(2-CHLOROPHENYL)-O-BENZYL-N-(BENZYLOXYCARBONYL)-L-TYROSYL-(2-DECARBOXY-D/L-PROLIN-2-YL)-PHOSPHONATE

Compound with spectra: 2 NMR

BIS-(2-CHLOROPHENYL)-O-BENZYL-N-(BENZYLOXYCARBONYL)-L-TYROSYL-(2-DECARBOXY-D/L-PROLIN-2-YL)-PHOSPHONATE
SpectraBase Compound ID KnrWNcZ9a2D
InChI InChI=1S/C40H37Cl2N2O7P/c41-33-16-7-9-18-36(33)50-52(47,51-37-19-10-8-17-34(37)42)38-20-11-25-44(38)39(45)35(43-40(46)49-28-31-14-5-2-6-15-31)26-29-21-23-32(24-22-29)48-27-30-12-3-1-4-13-30/h1-10,12-19,21-24,35,38H,11,20,25-28H2,(H,43,46)/t35-,38?/m0/s1
InChIKey MSCNTDGXOWQGLQ-VYXSRHMVSA-N
Mol Weight 759.6 g/mol
Molecular Formula C40H37Cl2N2O7P
Exact Mass 758.171544 g/mol
Enantiomer InChIKey MSCNTDGXOWQGLQ-BBTPBECRSA-N

View Spectrum of BIS-(2-CHLOROPHENYL)-O-BENZYL-N-(BENZYLOXYCARBONYL)-L-TYROSYL-(2-DECARBOXY-D/L-PROLIN-2-YL)-PHOSPHONATE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

View Spectrum of BIS-(2-CHLOROPHENYL)-O-BENZYL-N-(BENZYLOXYCARBONYL)-L-TYROSYL-(2-DECARBOXY-D/L-PROLIN-2-YL)-PHOSPHONATE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
FMOC-TYR(TBU)-PRO-GLY-PNAFMOC-TYROSINE-(TBU)-PROLINE-GLYCINE-PARANITROANILINE
STYLISSMIDE_F;CYCLO-(TRANS-PRO-(1)-CIS-PRO-(2)-PHE-(3)-ASP-(4)-TRANS-PRO-(5)-ARG-(6)-PHE-(7))
PHAKELLISTATIN_16;CYCLO-(PRO-PHE-ASP-SER-ARG-ALA-VAL-THR-TYR);MAJOR_ISOMER
ROLLAMIDE_B
STYLOPEPTIDE_2
DIANTHIN-D;CYCLO-(GLY-(1)-SER-(2)-LEU-(3)-PRO-(4)-PRO-(59-ILE-(6)-PHE-(7))
STYLOPEPTIDE_1
LOLOATIN-A;CYClIC-(L-ASPARAGINYL-L-ASPARTYL-L-TYROSYL-L-VALYL-L-ORNITHINYL-L-LEUCYL-D-TYROSYL-L-PROLYL-L-PHENYLALANYL-D-PHENYLALANYL)
Tryprostatin B
JAPONICIN_A
Title Journal or Book Year
Elektrochemische Decarboxylierung vonL.-Threonin- und Oligopeptid-Derivaten unter Bildung vonN-Acyl-N, O-acetalen: Herstellung von Oligopeptiden mit Carboxamid-oder Phosphonat-C-Terminus Helvetica Chimica Acta 1989

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