Department of Chemistry, University of Wisconsin-Madison, 1101 University Ave, Madison, Wisconsin 53706, USA.
J Am Chem Soc. 2011 Oct 26;133(42):16901-10. doi: 10.1021/ja206230h. Epub 2011 Oct 3.
Aerobic oxidation reactions have been the focus of considerable attention, but their use in mainstream organic chemistry has been constrained by limitations in their synthetic scope and by practical factors, such as the use of pure O(2) as the oxidant or complex catalyst synthesis. Here, we report a new (bpy)Cu(I)/TEMPO catalyst system that enables efficient and selective aerobic oxidation of a broad range of primary alcohols, including allylic, benzylic, and aliphatic derivatives, to the corresponding aldehydes using readily available reagents, at room temperature with ambient air as the oxidant. The catalyst system is compatible with a wide range of functional groups and the high selectivity for 1° alcohols enables selective oxidation of diols that lack protecting groups.
有氧氧化反应一直受到广泛关注,但由于其合成范围的限制以及实际因素(如使用纯 O(2)作为氧化剂或复杂催化剂合成),它们在主流有机化学中的应用受到限制。在这里,我们报告了一种新的(bpy)Cu(I)/TEMPO 催化剂体系,该体系可使用易得的试剂,在室温下,以环境空气为氧化剂,高效且选择性地氧化广泛的伯醇,包括烯丙基、苄基和脂肪族衍生物,生成相应的醛。该催化剂体系与多种官能团兼容,并且对 1°醇的高选择性使得无需保护基团的二醇的选择性氧化成为可能。