Cyclic products of the Ugi reaction of aldehydo and keto carboxylic acids: chemoselective modification
β Scribed by Alan Tsaloev; Alexei Ilyin; Sergey Tkachenko; Alexandre Ivachtchenko; Dmitry Kravchenko; Mikhail Krasavin
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- French
- Weight
- 277 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A method for the chemoselective reduction of Ugi-type lactam amides at the lactam carbonyl functionality with borane complexes has been developed. The novel reduction products can be further manipulated synthetically to yield various novel N-and C-terminally active unnatural amino acid building blocks.
π SIMILAR VOLUMES
## Abstract A modified Hunsdiecker reaction is described for the degradation of the silver salts of acetic acidβ1β^14^C, acetic acidβ2β^14^C, propionic acidβ1β^14^C, propionic acidβ3β^14^C, nβbutyric acidβ1β^14^C and nβbutyric acidβ2β^14^C to carbon dioxide, silver bromide and an organic bromide co