About
Contact & Profiles
A5017258220
Research Areas
- Organoboron and organosilicon chemistry
- Catalytic Cross-Coupling Reactions
- Synthetic Organic Chemistry Methods
- Crystallization and Solubility Studies
- X-ray Diffraction in Crystallography
- Chemical Synthesis and Analysis
University of Delaware
2016
We report the first example of a boryl-Heck reaction using an electrophilic boron reagent. This palladium-catalyzed process allows for conversion terminal alkenes to trans-alkenyl boronic esters commercially available catecholchloroborane (catBCl). In situ transesterification rapid access variety esters, amides, and other alkenyl adducts.
10.1021/jacs.6b02914
article
EN
Journal of the American Chemical Society
2016-04-22
10.1002/chin.201641203
article
EN
ChemInform
2016-09-01
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