@article{2946deb0cadd4b0d96bf8708cbad909e,
title = "Palladium-Catalyzed Regio- and Stereoselective Carbothiolation of Terminal Alkynes with Azolyl Sulfides",
abstract = "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.",
author = "Masayuki Iwasaki and Nikola Topolov{\v c}an and Hao Hu and Yugo Nishimura and Glwadys Gagnot and {Na Nakorn}, Rungsaeng and Ramida Yuvacharaskul and Kiyohiko Nakajima and Yasushi Nishihara",
note = "Funding Information: This work was partly supported by ACT-C, JST, as well as a Grant-in-Aid for Scientific Research (KAKENHI) (No. 26810060) from JSPS, and the Program for Promoting the Enhancement of Research Universities from MEXT and a Special Project of Okayama University. The authors gratefully thank Ms. Megumi Kosaka and Mr. Motonari Kobayashi (Department of Instrumental Analysis, Advanced Science Research Center, Okayama University) for measurement of elemental analyses and SC-NMR Laboratory of Okayama University for the NMR spectral measurements. Publisher Copyright: {\textcopyright} 2016 American Chemical Society.",
year = "2016",
month = apr,
day = "15",
doi = "10.1021/acs.orglett.6b00503",
language = "English",
volume = "18",
pages = "1642--1645",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "7",
}