359902-94-6Relevant articles and documents
Selective α-Oxyamination and Hydroxylation of Aliphatic Amides
Li, Xinwei,Lin, Fengguirong,Huang, Kaimeng,Wei, Jialiang,Li, Xinyao,Wang, Xiaoyang,Geng, Xiaoyu,Jiao, Ning
supporting information, p. 12307 - 12311 (2017/09/11)
Compared to the α-functionalization of aldehydes, ketones, even esters, the direct α-modification of amides is still a challenge because of the low acidity of α-CH groups. The α-functionalization of N?H (primary and secondary) amides, containing both an unactived α-C?H bond and a competitively active N?H bond, remains elusive. Shown herein is the general and efficient oxidative α-oxyamination and hydroxylation of aliphatic amides including secondary N?H amides. This transition-metal-free chemistry with high chemoselectivity provides an efficient approach to α-hydroxy amides. This oxidative protocol significantly enables the selective functionalization of inert α-C?H bonds with the complete preservation of active N?H bond.
Self-disproportionation of enantiomers of non-racemic chiral amine derivatives through achiral chromatography
Nakamura, Tsuyoshi,Tateishi, Kaori,Tsukagoshi, Shiori,Hashimoto, Saori,Watanabe, Shotaro,Soloshonok, Vadim A.,Ace?a, José Luis,Kitagawa, Osamu
experimental part, p. 4013 - 4017 (2012/07/14)
Efficient self-disproportionation of enantiomers of several non-racemic chiral amines was achieved through conversion to N-acetamides and subsequent MPLC using an achiral column. The MPLC of these non-racemic N-acetamide derivatives gave the chart having a clear boundary between two fractions. Thus, in the less polar fraction, remarkable enantiomer enrichment was observed (>99%ee), while the ee of more polar fraction was considerably reduced. The magnitude of the enantiomer enrichments and depletions strongly depended on substituent on the amino group.
