60729-85-3Relevant academic research and scientific papers
Blue light-promoted N–H insertion of amides, isatins, sulfonamides and imides into aryldiazoacetates: Synthesis of unnatural α-aryl amino acid derivatives
Okada, Celso Y.,dos Santos, Caio Y.,Jurberg, Igor D.
, (2020/07/03)
A photochemical protocol using blue light allows the N–H insertion of amides, isatins, sulfonamides and imides into aryldiazoacetates to afford the corresponding α-amino esters. This method is experimentally simple, inexpensive and tolerates numerous functional groups, thus allowing the straightforward preparation of a variety of α-aryl amino acid derivatives in good yields.
Amidoalkylation of Aromatics with Glyoxylic Acid-γ-Lactam Adducts: 2-Pyrrolidinone, Pyroglutamic Acid Amide and Ester
Roth, Ecaterina,Altman, Janina,Kapon, Moshe,Ben-Ishai, Dov
, p. 801 - 810 (2007/10/02)
A glyoxylic acid-2-pyrrolidinone adduct leads to N-acyliminium-ion induced intermolecular electrophilic aromatic substitution yielding nitrogen-substituted phenylglycine derivatives, whereas the benzylamide of glyoxylic acid-2-pirrolidinone adduct undergo
