Saavedra Carlos, Hernández Rosendo, Boto Alicia, Alvarez Eleuterio
Instituto de Productos Naturales y Agrobiología del CSIC, Avda. Astrofísico Francisco Sánchez 3, 38206-La Laguna, Tenerife, Spain.
J Org Chem. 2009 Jul 3;74(13):4655-65. doi: 10.1021/jo9004487.
The one-pot conversion of readily available alpha-amino acid into beta-amino acid derivatives was carried out in good yields. The method is a sequential process initiated by a tandem radical decarboxylation-oxidation reaction; the resulting acyliminium ion was trapped by silyl ketenes. Stoichiometric and catalytic versions of this reaction were developed and then applied to prepare modified di- and tripeptides. Interestingly, some tripeptides formed expanded beta-turns in the solid state.
将易得的α-氨基酸一锅法转化为β-氨基酸衍生物,产率良好。该方法是一个由串联自由基脱羧-氧化反应引发的连续过程;生成的酰亚胺离子被甲硅烷基烯酮捕获。开发了该反应的化学计量和催化版本,然后将其应用于制备修饰的二肽和三肽。有趣的是,一些三肽在固态下形成了扩展的β-转角。