Abstract
The results from a direct palladium-catalyzed cross-coupling reaction between a variety of olefins with acrylate through vinylic C–H activation that give the corresponding butadienes in moderate to good yields and stereoselectivities are reported. Given the reaction's ability to tolerate a wide range of styrenes, aliphatic alkenes and acrylates, this atom- and step-economical methodology offers a straightforward method to forge new C–C bonds of the valuable diene products from readily available starting materials under very mild reaction conditions.
Original language | English |
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Pages (from-to) | 4520-4524 |
Number of pages | 5 |
Journal | Chemical Science |
Volume | 4 |
Issue number | 12 |
DOIs | |
Publication status | Published - Oct 28 2013 |
Externally published | Yes |
ASJC Scopus Subject Areas
- General Chemistry