Benign Method for Alkene Epoxidations Benjamin S. Lane and Kevin Burgess* Department of Chemistry, Texas A & M UniVersity PO Box 30012, College Station, Texas 77842-3012 ReceiVed NoVember 17, 2000 This paper reports a simple method wherein manganese (2+) salts, for example, MnSO4, catalyze epoxidation of alkenes using 30% aqueous hydrogen peroxide as the terminal oxidant. The reactions are perf...

The importance of chiral epoxides as synthetic building blocks in asymmetric synthesis is extremely difficult to overstate. While the highly enantioselective Sharpless, and JacobsenKatsuki, protocols for the epoxidation of internal alkenes are nowmature technologies of inestimable value, the conversion of terminal alkenes to enantioenriched 1-oxiranes has proven a considerably more difficult pr...

The functionalization of alkenes is one the most important conversions in synthetic chemistry to prepare numerous fine chemicals. Typical procedures, such as hydrosilylation and hydroformylation, are traditionally catalyzed using homogeneous noble metal complexes, while highly reactive stable heterogeneous single-atom catalysts (SACs) now provide alternative approaches fulfill these by combinin...

Multi-step cascade reactions have gained increasing attention in the biocatalysis field recent years. In particular, multi-enzymatic cascades can achieve high molecular complexity without workup of reaction intermediates thanks to enzymes’ intrinsic selectivity; and where enzymes fall short, organo- or metal catalysts further expand range possible synthetic routes. Here, we present two enantioc...

The acidic group (-CO2H) of MultiWall Carbon Nanotube (MWCNT) converted to acyl chloride group (-COCl) producing of MVCNT@COCl. Then the reaction of MVCNT@COCl and MoO2(acac)2 resulted in direct immobilization of the MoO2(acac)2 and the formation of MVCNT@CO(acac)MoO2(acac) catalyst. In addition, the MVCNT@COCl was esterified...