(-)-FLUORENYL-9-METHOXYCARBONYL-LEUCINE-(N-TRIMETHYLSILANYLMETHY-2-ALLYL)-AMINOETHANOIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 1moCcMyeabp |
|---|---|
| InChI | InChI=1S/2C31H42N2O5Si/c2*1-8-13-28(30(35)37-4)33(20-39(5,6)7)29(34)27(18-21(2)3)32-31(36)38-19-26-24-16-11-9-14-22(24)23-15-10-12-17-25(23)26/h2*8-12,14-17,21,26-28H,1,13,18-20H2,2-7H3,(H,32,36)/t2*27-,28+/m00/s1 |
| InChIKey | ZTDMXIYOLFUULG-LONZTTGHSA-N |
| Mol Weight | 1101.5 g/mol |
| Molecular Formula | C62H84N4O10Si2 |
| Exact Mass | 1100.572598 g/mol |
| Enantiomer InChIKey | ZTDMXIYOLFUULG-IMVCZAQNSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(RAC)-CIS-1-FLUORENYL-9-METHOXYCARBONYL-LEUCINE-4-METHYLPYRROLIDINE-2-CARBOXYLIC-ACID-METHYLESTER
(RAC)-TRANS-1-FLUORENYL-9-METHOXYCARBONYL-LEUCINE-4-METHYLPYRROLIDINE-2-CARBOXYLIC-ACID-METHYLESTER
N-Fmoc-leu-pro-T-bu
N-(N-Fluorenyl-9-yl-methyloxycarbonyl-L-leucyl)-4R-hydroxy-L-proline methyl ester
N-FMOC-PHE-PRO-O-BU(T);MINOR-ISOMER
N-(9-FLUORENYLMETHYLOXYCARBONYL)-L-METHIONYLGLYCYL-L-LEUCYL-L-PROLINE
Propiolic acid, 3-[(fluorenylmethoxy)carbonylamino]-3-
#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
FMOC-PRO-SER(TBU)-PNAFMOC-PROLINE-SERINE(TBU-PARANITROANILINE
| Title | Journal or Book | Year |
|---|---|---|
| Photochemically Induced Electron Transfer (PET) Catalyzed Radical Cyclization: A Practical Method for Inducing Structural Changes in Peptides by Formation of Cyclic Amino Acid Derivatives | The Journal of Organic Chemistry | 2001 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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