Publication | Closed Access
Design and Synthesis of Chiral Oxathiozinone Scaffolds: Efficient Synthesis of Hindered Enantiopure Sulfinamides and Sulfinyl Ketimines
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Citations
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References
2013
Year
Combinatorial ChemistryBioorganic ChemistryOrganic ChemistryChemistryHindered Enantiopure SulfinamidesMedicinal ChemistrySo BondStereoselective SynthesisChiral Oxathiozinone ScaffoldsTitle ScaffoldsBulky SulfinamidesSulfinyl KetiminesPharmacologyNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNatural SciencesMedicineSynthetic ChemistryDrug Discovery
Is that SO? The title scaffolds have a highly active and properly differentiated SO bond for the efficient synthesis of enantiopure sulfinamides. The method is practical, green, and has the potential to provide an economical commercial process for the synthesis of bulky sulfinamides. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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