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Catalytic Asymmetric Epoxide Ring-opening Chemistry

Catalytic Asymmetric Epoxide Ring-opening Chemistry [Pg.229]


Catalytic Asymmetric Epoxide Ring-opening Chemistry... [Pg.229]

Catalytic asymmetric epoxide ring-opening chemistry 06M116. [Pg.52]

Jacobsen reported in 1990 that Mnm complexes of chiral salen ligands (41) were the most efficient catalysts available for the enantioselective epoxidation of alkyl- and aryl-substituted olefins.118 This stimulated a rapid development in the chemistry and applications of chiral SB complexes, which offer promising catalytic applications to several organic reactions, such as enantioselective cyclopropanation of styrenes, asymmetric aziridination of olefins, asymmetric Diels-Alder cycloaddition, and enantioselective ring opening of epoxides.4,119... [Pg.426]


See other pages where Catalytic Asymmetric Epoxide Ring-opening Chemistry is mentioned: [Pg.156]    [Pg.244]    [Pg.223]    [Pg.158]   


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Asymmetric catalytic

Asymmetric chemistry

Asymmetric epoxidation

Asymmetric epoxidation-ring

Asymmetric epoxide opening

Catalytic asymmetric epoxidation

Catalytic chemistry

Epoxidation catalytic

Epoxidation/ring-opening

Epoxidations, asymmetric

Epoxidations, catalytic

Epoxidations, catalytic asymmetric

Epoxide chemistry

Epoxide openings

Epoxide ring openings

Epoxides asymmetric epoxidation

Epoxides chemistry

Epoxides ring opening

Ring Chemistry

Ring asymmetric

Ring epoxides

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