Results 331 to 340 of about 171,419 (381)
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Journal of the American Chemical Society, 2014
Porous heterogeneous catalysts play a pivotal role in the chemical industry. Herein a new Hf-based metal-organic framework (Hf-NU-1000) incorporating Hf6 clusters is reported.
M. Beyzavi+9 more
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Porous heterogeneous catalysts play a pivotal role in the chemical industry. Herein a new Hf-based metal-organic framework (Hf-NU-1000) incorporating Hf6 clusters is reported.
M. Beyzavi+9 more
semanticscholar +1 more source
, 2016
The addition of water as a chain transfer reagent during the copolymerization reaction of epoxides and carbon dioxide has been shown as a promising method for producing CO2-based polycarbonate polyols.
Guang Wu, D. Darensbourg
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The addition of water as a chain transfer reagent during the copolymerization reaction of epoxides and carbon dioxide has been shown as a promising method for producing CO2-based polycarbonate polyols.
Guang Wu, D. Darensbourg
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Angewandte Chemie, 2016
We describe a regiodivergent epoxide opening (REO) featuring a catalyst-controlled synthesis of enantiomerically and diastereomerically highly enriched or pure syn- and anti- 1,3- and 1,4-difunctionalized building blocks from a common epoxide precursor ...
Nico Funken+2 more
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We describe a regiodivergent epoxide opening (REO) featuring a catalyst-controlled synthesis of enantiomerically and diastereomerically highly enriched or pure syn- and anti- 1,3- and 1,4-difunctionalized building blocks from a common epoxide precursor ...
Nico Funken+2 more
semanticscholar +1 more source
Tetrahedron, 1964
Abstract New preparative routes to the 13α,17aα-epoxide (II) and the 13β,17aβ-epoxide (III) are described. Boron trifluoride in benzene converts the α-epoxide (II) into a mixture from which five products were isolated, but the β-epoxide (III) gives only the 17aβ-hydroxy-Δ8(14)-olefin (VIII).
James M. Coxon+2 more
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Abstract New preparative routes to the 13α,17aα-epoxide (II) and the 13β,17aβ-epoxide (III) are described. Boron trifluoride in benzene converts the α-epoxide (II) into a mixture from which five products were isolated, but the β-epoxide (III) gives only the 17aβ-hydroxy-Δ8(14)-olefin (VIII).
James M. Coxon+2 more
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Epoxidation of homoisoflavones
Journal of Heterocyclic Chemistry, 2003AbstractA comparative study of the epoxidation of homoisoflavones (3‐benzyl‐4‐chromones) 1–4 has been performed by various oxidizing agents, víz. Epoxidation with isolated dimethyldioxirane (Method A), with alkaline hydrogen peroxide (Method B), and with sodium hypochlorite (Method C) to obtain the epoxides 4–8.
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Chemistry and Physics of Lipids, 2001
Previously unknown 4,5-epoxy-N-acetyl-sphingosine (1) was synthesized by epoxidation of N-acetyl-sphingosine with 1,1-dimethyldioxirane. A by-product generated by HPLC purification is the tetrahydrofuryl derivative of acetamide (2). Mainly allylic oxidation was observed when natural ceramides were reacted with dimethyldioxirane.
A, Möllenberg, G, Spiteller
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Previously unknown 4,5-epoxy-N-acetyl-sphingosine (1) was synthesized by epoxidation of N-acetyl-sphingosine with 1,1-dimethyldioxirane. A by-product generated by HPLC purification is the tetrahydrofuryl derivative of acetamide (2). Mainly allylic oxidation was observed when natural ceramides were reacted with dimethyldioxirane.
A, Möllenberg, G, Spiteller
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Enantioselectivities of yeast epoxide hydrolases for 1,2-epoxides
Tetrahedron: Asymmetry, 1999Abstract Kinetic resolution of homologous series of unbranched 1,2-epoxyalkanes (C-4 to C-12), 1,2-epoxyalkenes (C-4, C-6 and C-8), a 2,2-dialkylsubstituted epoxide (2-methyl-1,2-epoxyheptane) and a benzyloxy-substituted epoxide (benzyl glycidyl ether) was investigated using resting cells of 10 different yeast strains.
Botes, A.L.+3 more
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, 2015
In this study, we describe the substituent effect of epoxides on CO2/epoxide copolymerization catalyzed by a nanosized zinc–cobalt(III) double metal cyanide complex [Zn–Co(III) DMCC].
Xing-hong Zhang+4 more
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In this study, we describe the substituent effect of epoxides on CO2/epoxide copolymerization catalyzed by a nanosized zinc–cobalt(III) double metal cyanide complex [Zn–Co(III) DMCC].
Xing-hong Zhang+4 more
semanticscholar +1 more source
ChemInform, 1991
Publisher Summary The method for asymmetric epoxidation of alicyclic alcohols is known as Sharpless. The success of this method initiated much research into other techniques of asymmetric oxidation of alkenes in general and this chapter considers the progress in the area for the last six years.
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Publisher Summary The method for asymmetric epoxidation of alicyclic alcohols is known as Sharpless. The success of this method initiated much research into other techniques of asymmetric oxidation of alkenes in general and this chapter considers the progress in the area for the last six years.
openaire +2 more sources
, 2015
A new type of cascade biocatalysis was developed for one-pot enantioselective conversion of a meso- or racemic epoxide to an α-hydroxy ketone in high ee via an epoxide hydrolase-catalyzed hydrolysis of the epoxide, an alcohol dehydrogenase-catalyzed ...
Jiandong Zhang+3 more
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A new type of cascade biocatalysis was developed for one-pot enantioselective conversion of a meso- or racemic epoxide to an α-hydroxy ketone in high ee via an epoxide hydrolase-catalyzed hydrolysis of the epoxide, an alcohol dehydrogenase-catalyzed ...
Jiandong Zhang+3 more
semanticscholar +1 more source