Аннотация:
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.
Образец цитирования:
A. M. Agafontsev, N. B. Gorshkov, A. V. Tkachev, “Efficient synthesis of β-hydroxy sulfides by microwave-promoted ring opening in (+)-3-carene trans-epoxide with sodium thiolates”, Mendeleev Commun., 21:4 (2011), 192–193
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2912
https://www.mathnet.ru/rus/mendc/v21/i4/p192
Эта публикация цитируется в следующих 4 статьяx:
Zhihua Chen, Saeed Mohammadi Nasr, Mosstafa Kazemi, Masoud Mohammadi, “A Mini-Review: Achievements in the Thiolysis of Epoxides”, MROC, 17:4 (2020), 352
Serghei Curlat, “Recent Studies of (+)-3-Carene Transformations with the Retention of the Native Framework”, ChemJMold, 14:2 (2019), 32
Xiesi Quan, Shanfeng Yi, Xueye Wang, “Theoretical study of an anti-Markovnikov addition reaction catalyzed by β-cyclodextrin”, J Mol Model, 24:4 (2018)
Alexander M. Agafontsev, Nikolay B. Gorshkov, Alexey V. Tkachev, “ChemInform Abstract: Efficient Synthesis of β‐Hydroxy Sulfides by Microwave‐Promoted Ring Opening in (+)‐3‐Carene trans‐Epoxide with Sodium Thiolates.”, ChemInform, 42:50 (2011)
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