A novel catalytic route for the direct synthesis of bis-oxazolidinonedienes from CO2 and propargylic amines is presented. An inexpensive copper catalyst promotes the Glaser coupling and a subsequent double cyclization step. The obtained diene derivatives undergo polymerization in the solid state, showcasing a rare example of spontaneous topochemical polymerization.
Sequential Glaser reaction - diastereoselective cyclocarboxylation of propargylamines with CO 2 : a green catalytic access to bis-oxazolidinonedienes and their topochemical polymerization / Mele, F., Constantin, A.M., Sacchelli, F., Schiroli, D., Mazzeo, P.P., Maestri, G., Motti, E., Maggi, R., Mancuso, R., Gabriele, B., Pancrazzi, F., DELLA CA', N.. - In: GREEN CHEMISTRY. - ISSN 1463-9270. - (2024). [10.1039/d4gc00818a]
Sequential Glaser reaction - diastereoselective cyclocarboxylation of propargylamines with CO 2 : a green catalytic access to bis-oxazolidinonedienes and their topochemical polymerization
Francesco Mele;Ana Maria Constantin;Filippo Sacchelli;Debora Schiroli;Paolo Pio Mazzeo;Giovanni Maestri;Elena Motti;Raimondo Maggi;Francesco Pancrazzi;Nicola Della Ca'
2024-01-01
Abstract
A novel catalytic route for the direct synthesis of bis-oxazolidinonedienes from CO2 and propargylic amines is presented. An inexpensive copper catalyst promotes the Glaser coupling and a subsequent double cyclization step. The obtained diene derivatives undergo polymerization in the solid state, showcasing a rare example of spontaneous topochemical polymerization.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


