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Bulky Trialkylsilyl Acetylenes in the Cadiot−Chodkiewicz Cross-Coupling Reaction
110
Citations
24
References
2002
Year
Asymmetric CatalysisCross-coupling ReactionEnantioselective SynthesisDiyne Alcohol 10EngineeringAlkene MetathesisOrganic ChemistryOrganometallic CatalysisCatalysisBulky Trialkylsilyl-protected AlkynesChemistryStereoselective SynthesisCadiot-chodkiewicz Cross-coupling ReactionBulky Trialkylsilyl AcetylenesBiomolecular Engineering
Bulky trialkylsilyl-protected alkynes such as triethylsilyl (TES), tert-butyldimethylsilyl (TBS), and triisopropylsilyl (TIPS) acetylenes underwent the Cadiot-Chodkiewicz cross-coupling reaction with different bromoalkynes to form a variety of synthetically useful unsymmetrical diynes in good yields. The diyne alcohol 10 was transformed regio- and stereoselectively into enynes by hydrotelluration, carbometalation, and reduction reactions.
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