(RAC)-6-[METHOXYCARBONYL-(TRIMETHYLSILANYL)-METHYLAMINO]-7-TRITYLOXYHEPT-2-ENOIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
![(RAC)-6-[METHOXYCARBONYL-(TRIMETHYLSILANYL)-METHYLAMINO]-7-TRITYLOXYHEPT-2-ENOIC-ACID-METHYLESTER](/api/compound/4oYCB1ikbbb.png?ph=true&h=300&w=458 "(RAC)-6-[METHOXYCARBONYL-(TRIMETHYLSILANYL)-METHYLAMINO]-7-TRITYLOXYHEPT-2-ENOIC-ACID-METHYLESTER")
| SpectraBase Compound ID | 4oYCB1ikbbb |
|---|---|
| InChI | InChI=1S/C33H41NO5Si/c1-37-31(35)24-16-15-23-30(34(32(36)38-2)26-40(3,4)5)25-39-33(27-17-9-6-10-18-27,28-19-11-7-12-20-28)29-21-13-8-14-22-29/h6-14,16-22,24,30H,15,23,25-26H2,1-5H3/b24-16+ |
| InChIKey | KLIAQRIBPLDORC-LFVJCYFKSA-N |
| Mol Weight | 559.8 g/mol |
| Molecular Formula | C33H41NO5Si |
| Exact Mass | 559.2754 g/mol |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(6-HYDROXY-1-TRITYLOXYMETHYLHEX-4-ENYL)-(TRIMETHYLSILANYL)-METHYLCARBAMIC-ACID-METHYLESTER
(RAC)-ACETIC-ACID-6-[METHOXYCARBONYL-(TRIMETHYLSILANYL)-METHYLAMINO]-7-TRITYLOXYMETHYLHEPT-2-ENYLESTER
(RAC)-TRIMETHYLSILANYLMETHYL-(1-TRITYLOXYMETHYLPENT-4-ENYL)-CARBAMIC-ACID-TERT.-BUTYLESTER
(RAC)-TRANS-5-METHYL-2-TRITYLOXYMETHYLPIPERIDINE-1-CARBOXYLIC-ACID-METHYLESTER
(S)-1-(TERT.-BUTYLOXYCARBONYL)-5-(TRITYLOXYMETHYL)-2-PYRROLIDINONE
(S)-1-PHENYLMETHYL-5-(TRITYLOXYMETHYL)-2-PYRROLIDINONE
(5S)-1-[(2E)-3-Trimethylsilylprop-2-enoyl]-5-(triphenylmethoxymethyl)pyrrolidin-2-one
(ENT)-(-)-N-BENZYL-N-[(1S)-1-[(TRITYLOXY)-METHYL]-PROP-2-EN-1-YL]-BUT-3-ENAMIDE
1-(2-Hydroxy-3-trityloxy-propyl)-3-methyl-uracil
(+/-)-3-ALPHA-(6-METHOXYCARBONYL-2Z-HEXENYL)-2-BETA-TRIPHENYLMETHOXYMETHYL-1-ALPHA,4-ALPHA-CYClOPENTANEDIOL
| 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 |