## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
A facile synthesis of 2,5-diketopiperazines based on isocyanide chemistry
✍ Scribed by Stefano Marcaccini; Roberto Pepino; Ma̱ Cruz Pozo
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 56 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The Ugi four-component condensation (4-CC) between amines 4, aromatic aldehydes 5, chloroacetic acid 6 and isocyanides 7 afforded the expected 4-CC adducts 8 which were cyclised to the title compounds 9 upon treatment with ethanolic KOH under ultrasonication.
📜 SIMILAR VOLUMES
Ahs&act: Tbereactionbetween (E)-cinnamatdehyde(l), ebloroaeeticacid(2), cyclohexyl iaoeyanide (3), andamines 4affordcdtheexpeetcd Ugi4-CCproducta 5,whichwereeasitycyctisedto(E)-1-substituted N-cyclohexyl-2-( l-phenylcllmn-2-yl)4oxoazetidine-2-carboxarnides 6upontxeahnent wifhmetbanolic KOH. O 1997El
## Abstract Some new chirally pure 2,5‐substituted diketopiperazines were synthesized starting from 2‐methoxybenzyl alcohol. This multistep synthesis proceeds through the enzymatic synthesis of chirally pure amino acids, protection and dipeptide coupling, cyclization of dipeptide ester formates, an