4.8 Article

Palladium-Catalyzed Regio- and Stereoselective Carbothiolation of Terminal Alkynes with Azolyl Sulfides

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ORGANIC LETTERS
卷 18, 期 7, 页码 1642-1645

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b00503

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  1. JSPS [26810060]
  2. Program for Promoting the Enhancement of Research Universities from MEXT
  3. Okayama University
  4. ACT-C, JST
  5. Grants-in-Aid for Scientific Research [26810060] Funding Source: KAKEN

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Palladium-catalyzed carbothiolation of terminal alkynes with azolyl sulfides affords various 2-(azolyl)alkenyl sulfides with perfect regio- and stereoselectivities. The present addition reaction proceeded through a direct cleavage of carbon-sulfur bonds in azolyl sulfides. The resulting adducts that are useful intermediates in organic synthesis are further transformed to multisubstituted olefins containing azolyl moieties.

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