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- Chemistry
- Asymmetric Synthesis
- Chiral Building Blocks
- Chiral Catalysts, Chiral Ligands and Chiral Reagents
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- Catalysis Chemistry
- C-H Activation
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| Structure chimique | Catalogue N° | CAS N° | Formule | Masse moléculaire |
|---|
 |
BD229556 | 1072946-50-9 | C6H7BClNO3 | 187.39 |
| (6-Chloro-2-methoxypyridin-3-yl)boronic acid | ||||
 |
BD19127 | 193954-26-6 | C19H19NO4 | 325.36 |
| Fmoc-β-HoAla-OH | ||||
 |
BD130904 | 88743-97-9 | C30H34N4O6S | 578.68 |
| Fmoc-Arg(Mts)-OH | ||||
 |
BD18833 | 170899-08-8 | C10H17NO4 | 215.25 |
| (R)-2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid | ||||
 |
BD17624 | 114872-98-9 | C9H9Cl2NO2 | 234.08 |
| 2,4-Dichloro-D-phenylalanine | ||||
 |
BD34481 | 50428-03-0 | C5H7NO2 | 113.11 |
| 2-Aminopent-4-ynoic acid | ||||
 |
BD18828 | 170642-28-1 | C20H19NO4 | 337.37 |
| Fmoc-D-Gly(allyl)-OH | ||||
 |
BD18529 | 152338-45-9 | C27H22N2O5 | 454.47 |
| Fmoc-Trp(For)-OH | ||||
 |
BD282914 | 187458-77-1 | C6H12ClNO4 | 197.62 |
| (R)-4-Amino-5-methoxy-5-oxopentanoic acid hydrochloride | ||||
 |
BD230376 | 106402-41-9 | C7H16ClNO3 | 197.66 |
| H-Ser-Otbu.HCl | ||||