The solid phase synthesis of 1,3,4,7-Tetrasubstituted Perhydro-l,4-diazepine-2,5-diones is described. Starting from the resin-bound tBu ester ofaspartic acid and employing reductive alkylation and
Polymer-supported synthesis of diverse perhydro-1,4-diazepine-2,5-diones
✍ Scribed by Viktor Krchňák; Aleksandra S. Weichsel
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 178 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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## Abstract Synthesis of new 6‐(4‐chlorophenyl)perhydro‐1,3‐diazepine‐2,4‐diones was accomplished starting from 4‐amino‐3‐(4‐chlorophenyl)butyric acid (Baclofen). The chemical pathway involved the cyclisation of various 3‐(4‐chlorophenyl)‐4‐ureidobutyric acids. However, none of the new derivatives
We report here the synthesis of 3,7-disubstituted perhydro-1,4-diazepine-2,5-diones from amino acids and b-amino acids using a backbone amide linker (BAL) as a cis-configuration inductor. We have optimized each steps of the synthesis on solid support using Mimotopes crowns.