AI Article Synopsis
- A newly developed chiral diene ligand in a rhodium complex enables efficient conjugate additions.
- This process involves alkenes that are activated by both π-deficient and π-excessive heteroarenes.
- The result is highly enantioselective reactions with different arylboronic acids.
Article Abstract
In the presence of a rhodium complex containing a newly developed chiral diene ligand, alkenes activated by a range of π-deficient or π-excessive heteroarenes engage in highly enantioselective conjugate additions with various arylboronic acids.
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| http://dx.doi.org/10.1021/ja106809p | DOI Listing |
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