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- Chemistry
- Asymmetric Synthesis
- Chiral Building Blocks
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- Catalysis Chemistry
- C-H Activation
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| Structure chimique | Catalogue N° | CAS N° | Formule | Masse moléculaire |
|---|
 |
BD318814 | 1284228-59-6 | C11H13Cl2NO2 | 262.13 |
| (3R,4S)-rel-4-(3-Chlorophenyl)pyrrolidine-3-carboxylic acid hydrochloride | ||||
 |
BD314446 | 1227594-72-0 | C8H9NO3 | 167.16 |
| 2-Methoxy-5-methylnicotinic acid | ||||
 |
BD318554 | 1217722-51-4 | C10H13BrClNO2S | 326.64 |
| (S)-2-((5-Bromothiophen-2-yl)methyl)pyrrolidine-2-carboxylic acid hydrochloride | ||||
 |
BD318561 | 959578-37-1 | C15H21NO4S | 311.40 |
| (R)-1-(tert-Butoxycarbonyl)-2-(thiophen-3-ylmethyl)pyrrolidine-2-carboxylic acid | ||||
 |
BD318559 | 1217714-91-4 | C15H21NO4S | 311.40 |
| (S)-1-(tert-Butoxycarbonyl)-2-(thiophen-3-ylmethyl)pyrrolidine-2-carboxylic acid | ||||
 |
BD318565 | 959582-72-0 | C15H21NO5 | 295.33 |
| (R)-1-(tert-Butoxycarbonyl)-2-(furan-2-ylmethyl)pyrrolidine-2-carboxylic acid | ||||
 |
BD318553 | 959578-32-6 | C15H21NO4S | 311.40 |
| (R)-1-(tert-Butoxycarbonyl)-2-(thiophen-2-ylmethyl)pyrrolidine-2-carboxylic acid | ||||
 |
BD318556 | 1049729-23-8 | C10H13BrClNO2S | 326.64 |
| (R)-2-((5-Bromothiophen-2-yl)methyl)pyrrolidine-2-carboxylic acid hydrochloride | ||||
 |
BD245564 | 959581-51-2 | C17H22ClNO4 | 339.81 |
| (2S,4R)-1-(tert-Butoxycarbonyl)-4-(2-chlorobenzyl)pyrrolidine-2-carboxylic acid | ||||
 |
BD316189 | 946681-81-8 | C13H19N3O3 | 265.31 |
| 2-(2,2-Dimethyl-propionylamino)-N-methoxy-N-methyl-isonicotinamide | ||||