| Title | Highly Practical Copper(I)/TEMPO Catalyst System for Chemoselective Aerobic Oxidation of Primary Alcohols |
| Publication Type | Journal Article |
| Year of Publication | 2011 |
| Authors | Hoover, JM, Stahl, SS |
| Journal | Journal of the American Chemical Society |
| Volume | 133 |
| Pagination | 16901-16910 |
| Date Published | Oct |
| Accession Number | WOS:000296678200038 |
| Keywords | A, 1982, journal of scientific & industrial research, v41, p484, ATERBURN JB, 2001, TETRAHEDRON, V57, P9765, carbonyl-compounds, Chaudhuri P, 1998, ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, V37, P2217, chemistry, CIRIMINNA IL, 2010, ORG PROCESS RES DEV, V14, P245, Clarke PA, 2007, TETRAHEDRON, V63, P9124, Constable DJC, 2007, GREEN CHEMISTRY, V9, P411, dimethyl-sulfoxide, galactose-oxidase, Geisslmeier D, 2005, MONATSHEFTE FUR CHEMIE, V136, P1591, MANCUSO AJ, 1979, JOURNAL OF ORGANIC CHEMISTRY, V44, P4148, mild conditions, molecular-oxygen, N-propylammonium perruthenate, palladium(ii)-catalyzed oxidation, PFITZNER KE, 1963, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, V85, P3027, propargylic alcohols, Ragagnin G, 2002, TETRAHEDRON, V58, P3985, secondary alcohols, selective oxidation, SS DB, 1983, JOURNAL OF ORGANIC CHEMISTRY, V48, P4155, Steinhoff BA, 2004, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, V126, P11268, TOJO G, 2010, OXIDATION ALCOHOLS A,, Uyanik M, 2009, CHEMICAL COMMUNICATIONS, P2086 |
| Abstract | 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 degrees alcohols enables selective oxidation of diols that lack protecting groups. |
| Weight | 2 |
| Short Title | J. Am. Chem. Soc. |