2005
DOI: 10.1021/cr0406458
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Advances in Homogeneous and Heterogeneous Catalytic Asymmetric Epoxidation

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Cited by 927 publications
(325 citation statements)
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References 590 publications
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“…[6] We note that a number of dinuclear manganese complexes are of catalytic interest given their potential for catecholase activity, [7] whilst manganese Schiff-base complexes have also attracted attention for their antibacterial properties, [8] and have also been extensively employed in organic chemistry, for example as catalysts for asymmetric epoxidation. [9] As mentioned above, our interest stems from exploring the use of earth abundant transition metals as the metal centres in pre-catalysts for ROP, and herein, we have screened the manganese complexes for their ability to act as pre-catalysts in the ring opening polymerization (ROP) of ε-caprolactone; there is a lack of other Mn-based systems utilized in ROP of cyclic esters. [10] (1) was isolated in moderate yield (ca.…”
Section: Introductionmentioning
confidence: 99%
“…[6] We note that a number of dinuclear manganese complexes are of catalytic interest given their potential for catecholase activity, [7] whilst manganese Schiff-base complexes have also attracted attention for their antibacterial properties, [8] and have also been extensively employed in organic chemistry, for example as catalysts for asymmetric epoxidation. [9] As mentioned above, our interest stems from exploring the use of earth abundant transition metals as the metal centres in pre-catalysts for ROP, and herein, we have screened the manganese complexes for their ability to act as pre-catalysts in the ring opening polymerization (ROP) of ε-caprolactone; there is a lack of other Mn-based systems utilized in ROP of cyclic esters. [10] (1) was isolated in moderate yield (ca.…”
Section: Introductionmentioning
confidence: 99%
“…Chiral epoxides constitute key building blocks for the synthesis of a wide range of important products [55]. In particular, the asymmetric epoxidation of a,b-unsaturated carbonyl compounds is an important and challenging transformation in organic synthesis [56].…”
Section: Enantioselective Lanthanide-catalyzed Epoxidation Reactions mentioning
confidence: 99%
“…The selective oxidation of alkenes is of significant importance in the fine chemicals and pharmaceutical industries, since epoxides are key building blocks in organic synthesis [1][2][3]. Traditionally, epoxides are produced by the epoxidation of alkenes with stoichiometric amount of peracid as oxidant, which is hazardous and environmentally undesirable.…”
Section: Introductionmentioning
confidence: 99%
“…Due to the inherent advantages of heterogeneous catalysts over homogeneous ones, a number of solid catalysts have been developed [21]. Simple transition metal oxides like NiO, CoOx, MoO 3 and CuO show high activities for the selective epoxidation of styrene to styrene oxide [22]. Sulfated Y-ZrO 2 is as well active for the epoxidation of styrene with molecular oxygen [23].…”
Section: Introductionmentioning
confidence: 99%