Synthesis of small organic molecules using rhodium (isoquinolone derivatives), iron (alkylated arene derivatives), and zinc catalysis (alkylated arene derivatives), including protoberberine derivatives with potential herbicidal activity. Alkylated arenes are produced via Friedel-Crafts reactions of unactivated alcohols using dual Bronsted/Lewis-acid catalysis.
This solution offers access to small organic molecules synthesized through transition metal catalysis, including rhodium, iron, and zinc-based methods. The portfolio includes isoquinolone derivatives (rhodium catalysis), alkylated arene derivatives (iron and zinc catalysis), and protoberberine derivatives with potential herbicidal activity. A key methodology developed in the lab enables Friedel-Crafts reactions of unactivated (non-benzylic, non-allylic, non-propargylic) alcohols via dual Bronsted/Lewis-acid catalysis, providing a route to alkylated arenes relevant to natural product synthesis. These capabilities support partners in agrochemical discovery and natural product-based research.
The research is at an academic proof-of-concept stage. Methodology has been developed and applied to the synthesis of alkylated arenes and natural products, with protoberberine derivatives identified as candidates with potential herbicidal activity. Further validation is needed to confirm biological efficacy and assess commercial readiness.
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