An Efficient and Mild Method for the Synthesis and Hydrazinolysis of N-Glyoxylamino Acid Esters
N-Glyoxylamino acid ester derivatives were synthesized via the ring opening of N-acetylisatin using moderate conditions. During the hydrazinolysis of N-glyoxylamino acid ester derivatives with hydrazine hydrate (80%) in methanol, unexpected reduction of the α-keto group occurred to afford N-acylamin...
Saved in:
| Main Authors: | Ayman El-Faham, Zainab Al Marhoon, Ahmed Abdel-Megeed, Mohamed Siddiqui |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2013-01-01
|
| Series: | Journal of Chemistry |
| Online Access: | http://dx.doi.org/10.1155/2013/901745 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
synthesis of novel n-Substituted phthalimidyl esters and thier applications
by: Baghdad Science Journal
Published: (2006-12-01) -
Selective Synthesis of Fatty Alcohols over Mild Reaction Conditions via Non-Catalytic Liquid-Phase Fatty Acid Methyl Esters’ Reduction
by: Alejandro Vallejo Orrego, et al.
Published: (2023-11-01) -
A Convenient Synthesis and Antibacterial Activity of Novel α-Aminophosphonic Acid Esters from Amino Acids/Esters (Kabachnik-Fields Reaction)
by: CH. Mohan, et al.
Published: (2008-01-01) -
Corrigendum to “Synthesis of Kojic Ester Derivatives as Potential Antibacterial Agent”
by: Carolynne Zie Wei Sie, et al.
Published: (2019-01-01) -
Green Synthesis of Acid Esters from Furfural via Stobbe Condensation
by: Shubhra Banerjee, et al.
Published: (2013-01-01)