Department of Chemistry, University of Wisconsin-Madison, Madison, WI-53706, USA.
Discovery Chemistry, Merck & Co., Inc., 33 Avenue Louis Pasteur, Boston, MA-02115, USA.
Angew Chem Int Ed Engl. 2023 Apr 24;62(18):e202300178. doi: 10.1002/anie.202300178. Epub 2023 Mar 22.
Herein, we describe a practical protocol for the removal of alcohol functional groups through reductive cleavage of their benzoate ester analogs. This transformation requires a strong single electron transfer (SET) reductant and a means to accelerate slow fragmentation following substrate reduction. To accomplish this, we developed a photocatalytic system that generates a potent reductant from formate salts alongside Brønsted or Lewis acids that promote fragmentation of the reduced intermediate. This deoxygenation procedure is effective across structurally and electronically diverse alcohols and enables a variety of difficult net transformations. This protocol requires no precautions to exclude air or moisture and remains efficient on multigram scale. Finally, the system can be adapted to a one-pot benzoylation-deoxygenation sequence to enable direct alcohol deletion. Mechanistic studies validate that the role of acidic additives is to promote the key C(sp )-O bond fragmentation step.
在此,我们描述了一种通过还原苯甲酸酯类似物来去除醇官能团的实用方案。这种转化需要一种强的单电子转移(SET)还原剂和一种在底物还原后加速缓慢断裂的方法。为此,我们开发了一种光催化体系,可从甲酸盐盐中生成一种有效的还原剂,同时使用布朗斯特或路易斯酸促进还原中间体的断裂。这种脱氧程序在结构和电子上多样化的醇中都很有效,并能够实现各种困难的净转化。该方案不需要采取任何措施来排除空气或水分,并且在大规模生产中仍然有效。最后,该体系可以适应一锅法的苯甲酰化-脱氧序列,以实现直接的醇消除。机理研究证实,酸性添加剂的作用是促进关键的 C(sp )-O 键断裂步骤。