Department of Chemistry and Chemical Biology, Harvard University,12 Oxford Street, Cambridge, Massachusetts 02138, USA.
Org Lett. 2010 Mar 5;12(5):1024-7. doi: 10.1021/ol100032u.
The reaction rates and products in enantioselective Diels-Alder reactions with a range of dienophiles correlate with the expected degree of concertedness of bond formation in the transition state.
在手性 Diels-Alder 反应中,与一系列亲双烯体的反应速率和产物与过渡态中键形成的协同程度相符。