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9-FLUORENYL-METHYLOXYCARBONYL-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL

Compound with spectra: 1 NMR

9-FLUORENYL-METHYLOXYCARBONYL-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL
SpectraBase Compound ID 83iLYcG6ecM
InChI InChI=1S/C37H49N5O11S/c1-20(2)30(42-32(45)29(18-54-19-38-22(4)43)40-31(44)21(3)39-36(50)53-37(5,6)7)34(48)51-17-28(33(46)47)41-35(49)52-16-27-25-14-10-8-12-23(25)24-13-9-11-15-26(24)27/h8-15,20-21,27-30H,16-19H2,1-7H3,(H,38,43)(H,39,50)(H,40,44)(H,41,49)(H,42,45)(H,46,47)/t21-,28+,29-,30-/m0/s1
InChIKey ZTPMNZXBKMVRFF-MMNYTADISA-N
Mol Weight 771.9 g/mol
Molecular Formula C37H49N5O11S
Exact Mass 771.314929 g/mol
Enantiomer InChIKey ZTPMNZXBKMVRFF-YDRLCCHASA-N

View Spectrum of 9-FLUORENYL-METHYLOXYCARBONYL-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-HYDROXYL

13C NMR Spectrum
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Solvent DMSO-D6
9-FLUORENYL-METHYLOXYCARBONYL-D-SERINE-[N-BUTYLOXYCARBONYL-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL
N-(9-FLUORENYLMETHYLOXYCARBONYL)-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLINE
N-Fmoc-Leu-Pro-t-Bu
1-[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methyl-pentanoyl]ethylenimine-2,3-dicarboxylic acid diethyl ester
N-(FLUOREN-9-YLMETHOXYCARBONYL)-4-(TERT.-BUTYLESTER)-L-ASPARTIC-ACID-[2-(ALPHA-D-MANNOPYRANOSYLOXY)-ETHYL]-AMIDE
2-(N-Fluoren-9-ylmethoxycarbonylamino)-3-(tert-butyloxycarbonylamino)-3-(tolylthiocarbonyl)-1-phenylpropane
N-ALPHA-(FLUORENYL-9-METHOXYCARBONYL)-(1-NITROPHENYLETHYL-2-CYANOETHYL)-L-SERINE-TERT.-BUTYLESTER
N-(FLUOREN-9-YLMETHOXYCARBONYL)-4-[2-(ALPHA-D-MANNOPYRANOSYLOXY)-ETHYLAMIDO]-L-ASPARTIC-ACID-TERT.-BUTYLESTER
2-(N-Fluoren-9-ylmethoxycarbonylamino)-2-benzyl-1-(benzylamino)-1-(4'-tolylthiocarbonyl)ethane
2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[1-[tri(phenyl)methyl]imidazol-4-yl]propionic acid
Title Journal or Book Year
Solution-Phase Synthesis of Nucleobase-Substituted Analogues of Triostin A The Journal of Organic Chemistry 2004
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