Department of Chemistry, University of California, Irvine, California 92697-2025, USA.
Org Lett. 2011 Oct 7;13(19):5188-91. doi: 10.1021/ol202068p. Epub 2011 Aug 25.
Complementary stereospecific and stereoconvergent reactions for enantioselective synthesis of 1,3-oxazolidines are reported. In the presence of a rhodium catalyst, reaction of enantioenriched butadiene monoxide with aryl imines is stereospecific (99% ee). Alternatively, the reaction of racemic butadiene monoxide, in the presence of a chiral palladium or nickel catalyst, provides an enantioselective synthesis of 1,3-oxazolidines (up to 94% ee). Synthesis of either the cis- or trans-1,3-oxazolidines is also accomplished under catalyst control.
报道了用于立体选择性合成 1,3-恶唑烷的对映体专一和对映体转化的补充立体反应。在铑催化剂的存在下,与芳基亚胺反应的手性富集的丁二烯氧化物是立体专一的(99%ee)。或者,在手性钯或镍催化剂的存在下,外消旋的丁二烯氧化物的反应提供了 1,3-恶唑烷的对映选择性合成(高达 94%ee)。在催化剂控制下也可以完成顺式或反式 1,3-恶唑烷的合成。