| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280073 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
An original strategy combining a Hunsdiecker-type bromodecarboxylation and a Suzuki cross-coupling reaction starting from various cinnamic acids has been developed in one-pot and under microwave heating to give trans-1,2-diarylethenes in few minutes.
Graphical abstractThis Letter describes an efficient one-pot synthesis of trans-1,2-diarylethenes from cinnamic acids using microwave irradiation.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Marc-Antoine Bazin, Laïla El Kihel, Jean-Charles Lancelot, Sylvain Rault,