Synlett p. 891 - 892 (1997)
Update date:2022-07-31
Topics:
Yang, De-Yu
Huang, Xian
The hydroboration of dialkylselenoacetylenes 1, generated from alkylseleno bromides and sodium acetylide in liquid ammonia, with dicycloalkylboranes followed by iodination under basic condition produced (Z)/(E)-vinylic diselenides (2/3). The reaction proceeds with a transfer of one cycloalkyl group and smoothly to give major 2 and minor 3 in almost quantitative ratio (2:3=93:7 to 97:3). The hydroboration-iodination process provides a general method for synthesis of (Z)-vinylic diselenides containing cyclic systems.
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Doi:10.1021/ja971786c
(1997)Doi:10.1016/S0040-4039(01)99157-9
(1968)Doi:10.1016/j.ijpharm.2011.07.010
(2011)Doi:10.1016/j.tetlet.2005.06.017
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(1997)Doi:10.1016/S0040-4039(97)10024-7
(1997)
