Molas Jenna C, Poag Emily M, Ellman Jonathan A
Department of Chemistry, Yale University, New Haven, Connecticut 06520, United States.
Org Lett. 2024 Oct 11;26(40):8527-8531. doi: 10.1021/acs.orglett.4c03105. Epub 2024 Sep 27.
A two-step, diversity-building sequence to prepare monodehydro-diketopiperazines from readily accessible materials is reported. Rh(III)-catalyzed, amine-directed N-H functionalization of a variety of α-amino amides with a diazophosphonate ester and subsequent cyclization gives phosphonate-substituted diketopiperazines. A Horner-Wadsworth-Emmons reaction then provides monodehydro-diketopiperazines with high -alkene selectivity. This transformation was used to incorporate a variety of groups originating from diverse aldehydes and ketones with different steric and electronic properties. Face-selective hydrogenation to diketopiperazines is also disclosed.
报道了一种两步构建多样性的序列,用于从容易获得的原料制备单脱氢二酮哌嗪。铑(III)催化的各种α-氨基酰胺与重氮膦酸酯的胺导向N-H官能化反应以及随后的环化反应得到膦酸酯取代的二酮哌嗪。然后,霍纳-沃兹沃思-埃蒙斯反应提供具有高烯烃选择性的单脱氢二酮哌嗪。该转化反应用于引入源自具有不同空间和电子性质的各种醛和酮的多种基团。还公开了对二酮哌嗪的面选择性氢化反应。