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Selenosilanes Mediated Stereoselective Synthesis of Polyfunctionalized Organic Molecules
14
Citations
19
References
2008
Year
EngineeringNatural SciencesDiversity-oriented SynthesisSitu TreatmentOrganic ChemistrySynthetic ChemistryStereoselective SynthesisChemistryβ -Amino DiselenidesEfficient ReagentEnantioselective SynthesisBiomolecular Engineering
Bis(trimethylsilyl)selenide (HMDSS) acts as an efficient reagent in the TBAF catalyzed reaction with different substituted epoxides, episulfides, and aziridines, leading to β -functionalized diselenides in a highly regio- and stereoselective way. When using α -bromo alkyl ethers as trapping agent, 1,3-oxaselenolanes and 1,3-thiaselenolanes can be isolated, while 1,3-selenazolidines could be obtained through reduction of β -amino diselenides followed by in situ treatment with different aldehydes.
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