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Construction of Ge-Stereogenic Center by Desymmetric Carbene Insertion of Dihydrogermanes

Ai‐Cui Han, Li‐Jun Xiao, Qi‐Lin Zhou

2024Journal of the American Chemical Society34 citationsDOI

Abstract

We developed a method for the enantioselective synthesis of germanium-stereogenic compounds by the desymmetric carbene insertion of dihydrogermanes. A chiral rhodium phosphate catalyst decomposes diaryldiazo-methanes to generate rhodium carbenes that insert enantioselectively into one of the two Ge-H bonds of dihydrogermanes to form germanium-stereogenic compounds under mild reaction conditions. By this method, a variety of chiral germanes with germanium-stereogenic centers were synthesized in high yields and excellent enantioselectivities. Kinetic studies of the reaction showed that the diazo decomposition process was the rate-determining step. The remaining Ge-H bond of the chiral germane products provides a possibility for preparing chiral tetra-substituted germanium-stereogenic compounds.

Topics & Concepts

StereocenterChemistryCarbeneRhodiumDiazoGermaniumEnantioselective synthesisCatalysisStereochemistryWalden inversionCombinatorial chemistryMedicinal chemistryOrganic chemistrySiliconCyclopropane Reaction MechanismsSynthetic Organic Chemistry MethodsCatalytic C–H Functionalization Methods
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