FLUORENYL-9-METHOXYCARBONYL-ALANINE-(N-TRIMETHYLSILANYLMETHY-2-ALLYL)-AMINOETHANOIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | SdH80Hp4sa |
|---|---|
| InChI | InChI=1S/2C28H36N2O5Si/c2*1-7-12-25(27(32)34-3)30(18-36(4,5)6)26(31)19(2)29-28(33)35-17-24-22-15-10-8-13-20(22)21-14-9-11-16-23(21)24/h2*7-11,13-16,19,24-25H,1,12,17-18H2,2-6H3,(H,29,33)/t2*19-,25+/m00/s1 |
| InChIKey | GDFGJHKNVXHSDB-LPGWWCKBSA-N |
| Mol Weight | 1017.4 g/mol |
| Molecular Formula | C56H72N4O10Si2 |
| Exact Mass | 1016.478698 g/mol |
| Enantiomer InChIKey | GDFGJHKNVXHSDB-GNUMROAMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(RAC)-CIS-1-FLUORENYL-9-METHOXYCARBONYL-ALANINE-4-METHYLPYRROLIDINE-2-CARBOXYLIC-ACID-METHYLESTER
(RAC)-TRANS-1-FLUORENYL-9-METHOXYCARBONYL-ALANINE-4-METHYLPYRROLIDINE-2-CARBOXYLIC-ACID-METHYLESTER
Fmoc-Ala-Pro-OBn
(2S,3R)-2-[[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methyl-pentanoyl]amino]-3-hydroxy-3-phenyl-propionic acid methyl ester
{[N-(9-Fluorenylmethoxycarbonyl)phenylalanyl]-.alpha.-methylisoseryl}alanine tert-butyl ester
(2S)-3-(2,4-dimethoxyphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propionic acid tert-butyl ester
Fmoc-Benzothiazol-2-yl-alanine
(S)-3-(CARBONYL-9H-FLUOREN-9-YLMETHOXY)-4-(4-BENZYLOXYBENZYL)-OXAZOLIDIN-5-ONE
Fmoc-Phe-OPfp
4-[[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]propanoyl]amino]-3-iodanyl-benzoic acid
| 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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