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Nitroaldol reactions tandem inter-intramolecular asymmetric

F. Tandem inter-intramolecular catalytic, asymmetric nitroaldol reaction... [Pg.201]

Catalytic, Asymmetric Tandem Inter-Intramolecular Nitroaldol Reaction of98 with... [Pg.228]

Tandem Inter-Intramolecular Catalytic Asymmetric Nitroaldol Reaction... [Pg.154]

The asymmetric catalytic nitroaldol reaction was furthermore successfully extended to the field of asymmetric tandem reactions [31]. Tandem reactions are especially useful to construct compounds with several chiral centers in a one-pot synthesis starting from simple achiral components in the presence of a chiral catalyst. The first tandem inter-intramolecular catalytic asymmetric nitroaldol reaction has been realized in the reaction of the cyclopentanedione derivative 34 with nitromethane using a catalytic amount of LnLB according to Scheme 8 [31]. [Pg.154]

Figure 28. Proposed mechanism for the tandem inter- and intramolecular catalytic asymmetric nitroaldol reaction. Figure 28. Proposed mechanism for the tandem inter- and intramolecular catalytic asymmetric nitroaldol reaction.

See other pages where Nitroaldol reactions tandem inter-intramolecular asymmetric is mentioned: [Pg.227]    [Pg.172]   


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Asymmetric intramolecular

Asymmetric nitroaldol

Asymmetric nitroaldol reactions

Asymmetric reactions intramolecular

Nitroaldol

Nitroaldol reaction

Nitroaldolization

Nitroaldols

Tandem reactions

Tandem reactions reaction

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