Selective Photocyclization of Amino Acids in Dipeptides
Amino acids in dipeptides which are substituted at the N-atom by a benzoylalkyl group can be selectively photocyclized via a triplet biradical. With valine as amino acid the cyclization leads mainly to one product out of eight possible isomers.
| 主要な著者: | , , , |
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| フォーマット: | 論文 |
| 言語: | deu |
| 出版事項: |
Swiss Chemical Society
1997-01-01
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| シリーズ: | CHIMIA |
| オンライン･アクセス: | https://chimia.ch/chimia/article/view/2787 |