Single enantiomer synthesis of α-(trifluoromethyl)-β-lactam
The first synthesis of α-(trifluoromethyl)-β-lactam ((S)-1) is reported. The route starts from α-(trifluoromethyl)acrylic acid (2). Conjugate addition of α-(p-methoxyphenyl)ethylamine ((S)-3b), generated an addition adduct 4b which was cyclised to β-lactam 5b. Separation of the diastereoisomers by c...
| المؤلفون الرئيسيون: | , , |
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| التنسيق: | مقال |
| اللغة: | English |
| منشور في: |
Beilstein-Institut
2011-06-01
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| سلاسل: | Beilstein Journal of Organic Chemistry |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://doi.org/10.3762/bjoc.7.86 |