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Synthesis of I(III)/S(VI) reagents and their reactivity in photochemical cycloaddition reactions with unsaturated bonds nature.com/articles/s4146…

Synthesis of I(III)/S(VI) reagents and their reactivity in photochemical cycloaddition reactions with unsaturated bonds. go.nature.com/3T7l0mR

A Carbene Relay Strategy for Cascade Insertion Reactions. onlinelibrary.wiley.com/doi/10.1002/an…

onlinelibrary.wiley.com/doi/10.1002/an…

A Carbene Relay Strategy for Cascade Insertion Reactions (Yong Huang and co-workers) HKUST onlinelibrary.wiley.com/doi/10.1002/an…

Vinyltriarylbismuthonium Salts: Powerful Vehicles for α-Vinylation of Carbonyl Compounds J. Am. Chem. Soc. #Chemistry #Chemed #Science #TechnologyNews #news #technology #AcademicTwitter #ResearchPapers pubs.acs.org/doi/10.1021/ja…

Vinyltriarylbismuthonium Salts: Powerful Vehicles for α-Vinylation of Carbonyl Compounds | Journal of the American Chemical Society UChicago Chemistry The University of Chicago Total Synthesis and Methodology Highlights #Bismuth #Vinylation #Carbonyl pubs.acs.org/doi/10.1021/ja…

Online now: Transition metal-free difunctionalization of unactivated alkenes: Arylation/azidation, arylation/chlorination, and arylation/cyanation dlvr.it/TCjvG4

Proud to share our latest innovation from the Viresh Rawal lab at UChicago! We've pioneered a transition metal-free, light-driven method to transform alkenes, simplifying arylethylamine drug synthesis with sustainable chemistry. UChicago Chemistry Chem authors.elsevier.com/a/1jiDh8jWHELG…