141192-55-4Relevant academic research and scientific papers
Diastereoselective α-iodination reaction of 4-alkenylamide having a β-chiral center
Okada, Midori,Kitagawa, Osamu,Hanano, Tokushi,Taguchi, Takeo
, p. 6825 - 6834 (1997)
α-Iodination reaction of 4-alkenylamide with a β-chiral center proceeds with high diastereoseletivity to give syn α-iodoalkenamide through the formation of cyclic ketene N,O-acetal and subsequent α-iodination from the opposite side of a β-substituent.
A facile α-iodination reaction of unsaturated amides
Kitagawa,Hanano,Hirata,Inoue,Taguchi
, p. 1299 - 1302 (2007/10/02)
A novel and mild α-iodination of carboxamides was developed. Unsaturated amides could be converted to the α-iodoamides in moderate to good yields by treatment with I2 in the presence of s-collidine.
