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

Compound with spectra: 1 NMR

9-FLUORENYL-METHYLOXYCARBONYL-D-SERINE-[N-BUTYLOXYCARBONYL-L-ALANINE-L-CYSTEINE-(ACETAMIDOMETHYL)-L-VALINE]-O-TRICHLOROETHYL
SpectraBase Compound ID HSEsp7ce2NU
InChI InChI=1S/C39H50Cl3N5O11S/c1-21(2)31(47-33(50)30(18-59-20-43-23(4)48)45-32(49)22(3)44-37(54)58-38(5,6)7)35(52)55-17-29(34(51)57-19-39(40,41)42)46-36(53)56-16-28-26-14-10-8-12-24(26)25-13-9-11-15-27(25)28/h8-15,21-22,28-31H,16-20H2,1-7H3,(H,43,48)(H,44,54)(H,45,49)(H,46,53)(H,47,50)/t22-,29+,30-,31-/m0/s1
InChIKey QOXMCKWGIMIMKC-ZFXZTJKDSA-N
Mol Weight 903.3 g/mol
Molecular Formula C39H50Cl3N5O11S
Exact Mass 901.229312 g/mol
Enantiomer InChIKey QOXMCKWGIMIMKC-WMEZZDQISA-N

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

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#14B;[(Z)-D-SERINE-L-ALANINE-L-CYSTEINE-L-VALINE-9-FLUORENYL-METHYLOXYCARBONYL-D-SERINE-L-ALANINE-L-CYSTEINE-L-VALINE]-(SERINE-HYDROXYL)-DILACTONE-DISULFIDE
FMOC-CYS(TRT)-GLU(O-TERT.-BU)SCH2PPH2
N-(N-Fluorenyl-9-yl-methyloxycarbonyl-L-leucyl)-4R-hydroxy-L-proline methyl ester
(RAC)-TRANS-1-FLUORENYL-9-METHOXYCARBONYL-LEUCINE-4-METHYLPYRROLIDINE-2-CARBOXYLIC-ACID-METHYLESTER
(RAC)-CIS-1-FLUORENYL-9-METHOXYCARBONYL-LEUCINE-4-METHYLPYRROLIDINE-2-CARBOXYLIC-ACID-METHYLESTER
N-Fmoc-Leu-Pro-t-Bu
N-[(FLUOREN-9-YL)-METHOXYCARBONYL]-L-PROLYL-L-VALYL-2-METHYLALANYL-2-METHYLALANINE-DIMETHYLAMIDE
N-(9-FLUORENYLMETHYLOXYCARBONYL)-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLINE
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-sulfanylidene-4-(9H-xanthen-9-ylamino)butanoic acid
FMOC-PRO-SER(TBU)-PNAFMOC-PROLINE-SERINE(TBU-PARANITROANILINE
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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