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Schmidt, J.; Silks, L. A., Science of Synthesis, (2005) 18, 981.
The use of carbon diselenide for the construction of cyclic selenocarbamates is a straightforward process. However, a more general use of carbon diselenide is hindered by its propensity to polymerize under a variety of conditions. In addition, the commercial availability is limited. Despite its cost and limited availability, carbon diselenide is operationally easy to use and often simply adding it to a solution with a co-reactant such as 1,2-amino alcohol 37 and reagent will give rise to the product 38 as illustrated in Scheme 16.[53,54]
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Meeeeeeeeee-8-eeeeeee 88; Meeeeee Meeeeeeee:[88]
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References
[53] | Meeee, M.; Meeeeeeeee, M., Meeeeeeeeeee, (8888) 88, 888. |
[54] | Meeeee, M. M., M. Mee. Meee., (8888) 88, 8888. |