Some scientific research about 2-(2-Aminoacetamido)acetic acid

The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates. Interested yet? Read on for other articles about 556-50-3. Quality Control of 2-(2-Aminoacetamido)acetic acid.

As a society publisher, everything we do is to support the scientific community – so you can trust us to always act in your best interests, and get your work the international recognition that it deserves. 556-50-3, Name is 2-(2-Aminoacetamido)acetic acid, molecular formula is C4H8N2O3, belongs to pyrrolines compound, is a common compound. In a patnet, author is CABALLERO, E, once mentioned the new application about 556-50-3, Quality Control of 2-(2-Aminoacetamido)acetic acid.

N-SUBSTITUTED PYRROLINONES FROM ENAMINES AND ALPHA-DICARBONYLS

The reaction between N-substituted enamines and phenylglyoxal or glyoxal yielded Delta(2)-pyrrolin-5-ones in moderate to good yields. An uncommon pyrrolo [2,1-b]thiazole derivative was formed as a minor product when a N-(2-mercaptoethyl)enamine was used as the starting reagent. An explanation for the regiochemistry of the reaction is proposed.

The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic, their interactions with reaction intermediates. Interested yet? Read on for other articles about 556-50-3. Quality Control of 2-(2-Aminoacetamido)acetic acid.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem