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Attack Synthesis in Discrete Event Systems Under Asymmetric Observation Setting
Ruotian Liu +3 more
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Asymmetric Synthesis of (−)-Adaline
Organic Letters, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Toshimasa, Itoh +2 more
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ChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Ryo Shintani, Tamio Hayashi
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Ryo Shintani, Tamio Hayashi
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Magnetochirality-Induced Asymmetric Synthesis
ChemPhysChem, 2001Magnetochiral anisotropy, the combined effect of a collinear arrangement of a magnetic field B and the wave vector k of a light beam--as illustrated in the picture--has been proven to produce an enantiomeric excess in a chemical reaction, to make this effect a likely candidate for the origin of the homochirality of life.
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ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Ryoji Noyori +2 more
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AbstractFor Abstract see ChemInform Abstract in Full Text.
Ryoji Noyori +2 more
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Asymmetric Synthesis of Arboduridine
Angewandte Chemie, 2023AbstractThe first asymmetric total synthesis of the monoterpenoid indole alkaloid arboduridine has been accomplished. The tricyclic A/B/D ring system was constructed by an enantioselective Michael reaction followed by intramolecular nucleophilic addition. Intramolecular α‐amination of a ketone forged the piperidine ring, while a Horner–Wadsworth–Emmons
Rui Yang +5 more
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Asymmetric synthesis of (+)-abresoline
Tetrahedron Letters, 2005Abstract The first asymmetric synthesis of (+)-abresoline has been achieved starting from the ( S )-1-(aryl)homoallylic amine, which was prepared enantioselectively by the method based on allylation of the ( R )-2′-(2-naphthyl)-bearing hydroxyoxime ether.
Masakazu Atobe +2 more
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2023
The goal of asymmetric synthesis is the chemical conversion of a molecule into a specific stereoisomer (enantiomer). In spite of the fact that asymmetric chemistry can be conducted stoichiometrically, it is most commonly carried out in a catalytic mode, mainly by applying organometallic catalysts or an enzyme (biocatalysis)
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The goal of asymmetric synthesis is the chemical conversion of a molecule into a specific stereoisomer (enantiomer). In spite of the fact that asymmetric chemistry can be conducted stoichiometrically, it is most commonly carried out in a catalytic mode, mainly by applying organometallic catalysts or an enzyme (biocatalysis)
openaire +1 more source

