Catalytic Asymmetric Synthesis. Группа авторов

Catalytic Asymmetric Synthesis - Группа авторов


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of transfer hydrogenation using indoline as a hydrogen donor (a), oxidative kinetic resolution of indolines using ketimine (b), and oxidative kinetic resolution of indolines based on self-redox reaction (c)."/>

      Source: Based on [152]

      ), oxidative kinetic resolution of indolines using ketimine (b) (

      Source: Based on [153]

      ), and oxidative kinetic resolution of indolines based on self‐redox reaction (c) (

      Source: Based on [154]).

      2.6.2. Reduction of Ketones

      2.6.3. Reduction of Alkenes

Schematic illustration of transfer hydrogenation of chalcone derivatives.

      Source: Based on [156].

Schematic illustration of reduction of indolines.

      Source: Based on [157].

Schematic illustration of transfer hydrogenation of 1,1-diarylethenes.

      Source: Based on [158].

Schematic illustration of asymmetric spiroacetalization by confined Bronsted acid.

      Source: Based on [13].

Schematic illustration of asymmetric spiroacetalization by TRIP.

      Source: Based on [159].

Schematic illustration of intramolecular hydroamination of alkenes (a), and its application to desymmetrization of meso dienes (b).

      Source: Based on [160]

      ), and its application to desymmetrization of meso dienes (b) (

      Source: Based on [161]).

Schematic illustration of hydroarylation of 1,1-diarylethenes.
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