Formation of 1,1 '-iminodicarboxylic acid derivatives, 2,6-diketo-piperazine and dibenzodiazocine-2,6-dione by variations of multicomponent reactions

Citation
Ik. Ugi et al., Formation of 1,1 '-iminodicarboxylic acid derivatives, 2,6-diketo-piperazine and dibenzodiazocine-2,6-dione by variations of multicomponent reactions, CHEMOSPHERE, 43(1), 2001, pp. 75-81
Citations number
22
Categorie Soggetti
Environment/Ecology
Journal title
CHEMOSPHERE
ISSN journal
00456535 → ACNP
Volume
43
Issue
1
Year of publication
2001
Pages
75 - 81
Database
ISI
SICI code
0045-6535(200104)43:1<75:FO1'AD>2.0.ZU;2-2
Abstract
The combination of multicomponent reactions (MCRs) of different amino acids , aldehydes, isocyanides and acids allows complex structures to be prepared in one-pot reactions. The synthesis of I,l'-iminodicarboxylic acid derivat ives 12 demonstrates the high selectivity of the Ugi Four Component Reactio n using two different aldehydes and two different isocyanides. The limitati ons of the MCRs are illustrated by the synthesis of a l,l'-iminodicarboxyli c acid derivative 6 from L-lysine. Furthermore, 2,6-diketopiperazines and d ibenzodiazocin-2,6-diones are synthesized via MCRs. (C) 2001 Published by E lsevier Science Ltd. All rights reserved.