Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, USA.
Org Lett. 2013 Sep 6;15(17):4358-61. doi: 10.1021/ol401858k. Epub 2013 Aug 19.
Redox-neutral formation of C-P bonds in the α-position of amines was achieved via a process that features a combination of an oxidative α-C-H bond functionalization and a reductive N-alkylation. Benzoic acid functions as an efficient catalyst in this three-component reaction of cyclic secondary amines, aldehydes and phosphine oxides to provide rapid access to α-amino phosphine oxides not easily accessible by classic Kabachnik-Fields reactions.
通过氧化α-C-H 键官能化和还原 N-烷基化相结合的过程，实现了胺的α-位 C-P 键的氧化还原中性形成。在该三组分反应中，苯甲酸作为环状仲胺、醛和氧化膦的有效催化剂，为经典的 Kabachnik-Fields 反应不易获得的α-氨基氧化膦提供了快速途径。
