(RAC)-TRANS-4-METHYL-2-TRITYLOXYMETHYLPYRROLIDINE-1-CARBOXYLIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 7LopSx7biGO |
|---|---|
| InChI | InChI=1S/C27H29NO3/c1-21-18-25(28(19-21)26(29)30-2)20-31-27(22-12-6-3-7-13-22,23-14-8-4-9-15-23)24-16-10-5-11-17-24/h3-17,21,25H,18-20H2,1-2H3/t21-,25+/m1/s1 |
| InChIKey | LOBWDWSCZJHACW-BWKNWUBXSA-N |
| Mol Weight | 415.53 g/mol |
| Molecular Formula | C27H29NO3 |
| Exact Mass | 415.214744 g/mol |
| Enantiomer InChIKey | LOBWDWSCZJHACW-SQJMNOBHSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(RAC)-TRIMETHYLSILANYLMETHYL-(1-TRITYLOXYMETHYLBUT-3-ENYL)-CABAMIC-ACID-METHYLESTER
(RAC)-FORMYL-(1-TRITYLOXYMETHYLHEX-4-ENYL)-CARBAMIC-ACID-TERT.-BUTYLESTER
(-)-(4E)-6-O-ACETYL-2-[(TERT.-BUTOXYCARBONYL)-AMINO]-2,4,5-TRIDEOXY-1-O-TRITYL-D-ERYTHRO-HEX-4-ENITOL
(+)-TERT.-BUTYL-[[1S,2R,(3E)]-1-[(TRITYLOXY)-METHYL]-HEPTADEC-3-EN-1-YL]-CARBAMATE
(1R,4R,7S)-7-[(Trityloxy)methyl]-2-oxabicyclo[3.2.1]octan-3-one
(2-HYDROXYMETHYL-6-TRITYLOXYMETHYL-TETRAHYDRO-PYRAN-4-YLIDENE)-ACETIC-ACID-ETHYLESTER
(2-HYDROXYMETHYL-6-TRITYLOXYMETHYL-TETRAHYDRO-PYRAN-4-YLIDENE)-ACETIC-ACID-ISOPROPYLESTER
(2R,3R,5R)-2-ethenyl-3-(1-methylethenyl)-5-[(triphenylmethyl)oxymethyl]oxolane
(2R,4R,5R)-2,5-Dimethyl-4-(trityloxymethyl)-1,3-dioxan-5-ol
D-Mannitol, 2,5-bis-O-(phenylmethyl)-1,6-bis-O-(triphenylmethyl)-
| 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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