This article is cited in 4 papers

Efficient synthesis of β-hydroxy sulfides by microwave-promoted ring opening in (+)-3-carene trans-epoxide with sodium thiolates

A. M. Agafontsev^a, N. B. Gorshkov^a, A. V. Tkachev<sup>ab

a</sup> N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
^b Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation

Abstract: Reaction of (+)-3-carene trans-epoxide with sodium thiolates in methanolic solution in a microwave oven at 140°C for 35–40min affords corresponding (1S,3S,4S,6R)-4-sulfanylcaran-3-ols in 75–95% yields.

Language: English

DOI: 10.1016/j.mencom.2011.07.006

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