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404-24-0 | 2,2,2-Trifluoro-N-phenylacetamide
CAS No: 404-24-0 Catalog No: AG003V2D MDL No:MFCD00196027
Product Description
Catalog Number:
AG003V2D
Chemical Name:
2,2,2-Trifluoro-N-phenylacetamide
CAS Number:
404-24-0
Molecular Formula:
C8H6F3NO
Molecular Weight:
189.1345
MDL Number:
MFCD00196027
SMILES:
O=C(C(F)(F)F)Nc1ccccc1
Literature
| Title | Journal |
|---|---|
| Tuning the leaving group in 2-deoxy-2-fluoroglucoside results in improved activity-based retaining β-glucosidase probes. | Chemical communications (Cambridge, England) 20121028 |
| Studies on the selectivity between nickel-catalyzed 1,2-cis-2-amino glycosylation of hydroxyl groups of thioglycoside acceptors with C2-substituted benzylidene N-phenyl trifluoroacetimidates and intermolecular aglycon transfer of the sulfide group. | The Journal of organic chemistry 20120907 |
| Chemical synthesis of Helicobacter pylori lipopolysaccharide partial structures and their selective proinflammatory responses. | Chemistry (Weinheim an der Bergstrasse, Germany) 20111216 |
| Reinvestigation of the C5-acetamide sialic acid donor for α-selective sialylation: practical procedure under microfluidic conditions. | Organic & biomolecular chemistry 20111021 |
| Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. | Bioorganic & medicinal chemistry letters 20101101 |
| Synthesis of a sialic acid containing complex-type N-glycan on a solid support. | Chemistry, an Asian journal 20090406 |
| Synthesis of fructofuranosides: efficient glycosylation with N-phenyltrifluoroacetimidate as the leaving group. | Carbohydrate research 20081124 |
| Facile access to polysubstituted indoles via a cascade Cu-catalyzed arylation-condensation process. | The Journal of organic chemistry 20071123 |
| Assembly of conjugated enynes and substituted indoles via CuI/amino acid-catalyzed coupling of 1-alkynes with vinyl iodides and 2-bromotrifluoroacetanilides. | The Journal of organic chemistry 20070622 |
| Donor-bound glycosylation for various glycosyl acceptors: bidirectional solid-phase semisynthesis of vancomycin and its derivatives. | Chemistry, an Asian journal 20070108 |
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