New Advances in Chemical Research in 2021. Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage , causing turnover rates to depend strongly on interfacial structure. 7423-55-4, Name is 3-Maleimidopropionic acid, molecular formula is , belongs to pyrrolines compound. In a document, author is Rodriguez-Soria, Veronica, Application In Synthesis of 3-Maleimidopropionic acid.
A novel stereoselective tin-free radical protocol for the enantioselective synthesis of pyrrolidinones and its application to the synthesis of biologically active GABA-derivatives
Optically pure 4-alkyl-pyrrolin-2-ones were synthesized from chiral N-allyl-alpha-bromoacetamides in high selective and stereo-controlled fashion, via a sequential 5-exo-trig radical cyclization-hydrogen or bromine atom-transfer process, under non-tin conditions. Interestingly, when N-allyl-alpha-bromoacetamides were treated with triethylborane/MeOH(excess)/BF3 center dot OEt2 in toluene at -78 degrees C, a tandem 5-exo-trig radical cyclization-hydrogen atom-transfer reaction operated, on the other hand, a tandem 5-evo-trig radical cyclization-bromine atom-transfer reaction proceeded in good yield and high stereoselectivity when the reaction was carried out with equimolar amounts of MeOH in THF at -78 degrees C. Thus, optically pure 4-alkyl-pyrrolin-2-ones were synthesized via this tin-free radical pathway and transformed to their corresponding biologically active GABA-derivatives, Pregabalin and CAMP. (C) 2008 Published by Elsevier Ltd.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 7423-55-4, in my other articles. Application In Synthesis of 3-Maleimidopropionic acid.
Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem