Organic Letters · 2000 · 60 citations · 5 references
Natural SciencesChemistryCatalysisGreen ChemistryOrganic ChemistryHeterocyclic ChemistryProtecting-group StrategySulfur ChemistrySulfur CompoundsSelective AcylationSteric PropertiesThioester ChemistryThiol ChemistryThiol FunctionalizationThiols Protecting Groups
The thiol group is one of the few groups NOT tolerated by the Suzuki reaction. Therefore, a new protective group, the 2-methoxyisobutyryl group, was developed by tuning the electronic/steric properties of the acyl residue. Other thioesters, such as thioacetate, result in a more or less dominant side reaction, which to date has not been described: sulfur-assisted acylation of boronic acids. The reaction pathway for this new reaction is discussed.
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Protective groups in organic synthesis
Philip Hodge · Polymer · 1992 · 2.2K citations
Palladium-Catalyzed Cross-Coupling Reactions of Organoboronic Acids with Organic Electrophiles.
Arnold R. Martin, Youhua Yang, Domenico Spinelli et al. · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · 1993 · 205 citations · Full text
Richard P. Hsung, Christopher E. D. Chidsey, Lawrence R. Sita · Organometallics · 1995 · 118 citations