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Asymmetric Epoxidation with Polymeric Cinchona-PTCs

Asymmetric Epoxidation with Polymeric Cinchona-PTCs [Pg.63]

Besides the asymmetric alkylation of 1 for the synthesis of higher a-amino acid derivatives, the Park-Jew group applied their dimeric cinchona-PTCs to the [Pg.63]

The Park-Jew group proposed a possible transition state in which the chalcone is located between the two cinchona units in the catalyst 66, and the (1-phenyl moiety of chalcone has a k-k stacking interaction with one of the quinoline moieties in 66. [Pg.66]

Binaphthyl- and Biphenyl-Modified Chiral Phase-Transfer Catalysts for Asymmetric Synthesis [Pg.71]

Asymmetric Synthesis of a-Alkyl a-Amino Acids and Their Derivatives [Pg.71]


Asymmetric Epoxidation with Polymeric Cinchona-PTCs 63... [Pg.63]




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Asymmetric PTC

Asymmetric PTCs

Asymmetric epoxidation

Asymmetric polymeric PTCs

Asymmetric polymeric cinchona-PTCs

Cinchona

Cinchona epoxidation

Cinchona polymeric

Cinchona-PTCs

Epoxidations, asymmetric

Epoxide polymerization

Epoxides asymmetric epoxidation

PTC-124

Polymeric asymmetric epoxidation

Polymeric cinchona-PTCs

Polymerization asymmetric

Polymerization, with

With epoxides

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