Stereospecific Palladium-Catalyzed Cross-Coupling of Alkylboron Compounds: A Short Account

Abstract

AbstractStereospecific approaches allow the introduction of a stereogenic center into complex organic molecules using optically active reagents. Among these, the Pd-catalyzed stereospecific cross-coupling of chiral alkylboron compounds stands out as a highly effective tool for organic synthesis. In parallel with advances in the development of borylation technology, the strategy has recently witnessed a growth in its applicability. This account aims to review the progress on Pd-catalyzed stereospecific B-alkyl Suzuki–Miyaura cross-coupling, tracing its evolution from early breakthroughs to the most recent advances.1 Introduction2 Cross-Coupling of 1° Alkylboron Compounds3 Cross-Coupling of Benzylboron Compounds4 Cross-Coupling of Allyl- and Propargylboron Compounds5 Cross-Coupling of Other Types of Activated 2° Alkylboron Compounds6 Cross-Coupling of Unactivated 2° Alkylboron Compounds7 Conclusion and Outlook