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| Publications [#330258] of Michael J. Therien
Papers Published
- Gauthier, JY; Henien, T; Lo, L; Thérien, M; Young, RN, A novel and efficient method for the preparation of asymmetric dithioacetals,
Tetrahedron Letters, vol. 29 no. 51
(January, 1988),
pp. 6729-6732, Elsevier BV [doi]
(last updated on 2026/01/14)
Abstract: Aldehydes and ketones react with one equivalent each of thiols and thiolacetic acid under acid catalysis to yield almost exclusively the mixed alkylthio-(or arylthio-) acylthioacetals. Reaction of the mixed thioacetal with a nucleophile (such as NaOMe) liberates the thiolate anion which can be trapped with a variety of electrophiles to provide asymmetric dithioacetals in high yields. © 1988.
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