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.
| Main Authors: | , , , |
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| Format: | Article |
| Language: | deu |
| Published: |
Swiss Chemical Society
1997-01-01
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| Series: | CHIMIA |
| Online Access: | https://chimia.ch/chimia/article/view/2787 |