Organosulfur compounds: electrophilic reagents in transition-metal-catalyzed carbon-carbon bond-forming reactions |
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Authors: | Dubbaka Srinivas Reddy Vogel Pierre |
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Affiliation: | Laboratoire de glycochimie et de synthèse asymétrique Ecole Polytechnique Fédérale de Lausanne (EPFL), Switzerland. pierre.vogel@epfl.ch |
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Abstract: | Transition-metal-catalyzed carbon-carbon bond-forming reactions are among the most powerful methods in organic synthesis and play a crucial role in modern materials science and medicinal chemistry. Recent developments in the area of ligands and additives permit the cross-coupling of a large variety of reactants, including inexpensive and readily available sulfonyl chlorides. Their desulfitative carbon-carbon cross-coupling reactions (Negishi, Stille, carbonylative Stille, Suzuki-Miyaura, and Sonogashira-Hagihara-type cross-couplings and Mizoroki-Heck-type arylations) are reviewed together with carbon-carbon cross-coupling reactions with other organosulfur compounds as electrophilic reagents. |
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Keywords: | cross‐couplings homogeneous catalysis sulfonamides sulfonyl chlorides transition metals |
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