Kim, Sunggak published the artcileRadical-mediated γ-functionalizations of α,β-unsaturated carboxylic amides, Category: iodides-buliding-blocks, the publication is Angewandte Chemie, International Edition (2004), 43(40), 5378-5380, database is CAplus and MEDLINE.
Highly successful tin-free, radical-mediated alkylations of α,β-unsaturated carboxylic amides have been carried out. Alkyl iodides and bromides bearing α-electron-withdrawing groups undergo selective γ-additions to diene O,N-acetals. This approach to γ-functionalization was further extended to the use of hetero groups, such as phenylsulfanyl and phenylsulfonyl species.
Angewandte Chemie, International Edition published new progress about 31253-08-4. 31253-08-4 belongs to iodides-buliding-blocks, auxiliary class Iodide,Ester, name is Ethyl 2-Iodopropionate, and the molecular formula is C5H9IO2, Category: iodides-buliding-blocks.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com