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ChemInform Abstract: Diastereo‐ and Enantioselective Iridium Catalyzed Carbonyl (α‐Cyclopropyl)allylation via Transfer Hydrogenation.

Ryosuke Tsutsumi, Suckchang Hong, Michael J. Krische

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Abstract

Abstract Using the chiral precatalyst modified by SEGPHOS, the carbonyl α‐(cyclopropyl)allylation is reached with similar facility from alcohol or aldehyde oxidation levels of the substrates.

About this research paper

What this paper is about

Abstract Using the chiral precatalyst modified by SEGPHOS, the carbonyl α‐(cyclopropyl)allylation is reached with similar facility from alcohol or aldehyde oxidation levels of the substrates.

Why it matters

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Method / approach

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Available abstract

Abstract Using the chiral precatalyst modified by SEGPHOS, the carbonyl α‐(cyclopropyl)allylation is reached with similar facility from alcohol or aldehyde oxidation levels of the substrates.

Key concepts: Chemistry, Iridium, Transfer hydrogenation, Enantioselective synthesis, Catalysis, Asymmetric hydrogenation, Organic chemistry, Medicinal chemistry

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ChemInform Abstract: Diastereo‐ and Enantioselective Iridium Catalyzed Carbonyl (α‐Cyclopropyl)allylation via Transfer Hydrogenation. — Research Paper | ScholarLens