2023
DOI: 10.1002/asia.202300731
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The Development of Aldehyde Catalytic System

Jinli Chen,
Xiaoqun Yang,
Yixian Huang
et al.

Abstract: Aldehyde catalysts have proven to be highly effective in facilitating and accelerating a wide range of challenging transformations in organic chemistry. This article is structured into three main sections, focusing on the utilization of aldehydes as organocatalysts, the aldehydes/transition metals catalytic systems, and photochemical initiators. Finally, we provide a concise summary of the advancements in this fascinating research field, offering our perspectives and insights.

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“…Carbonyl compounds typically serve as reagents in organic synthesis. However, they can also be used as catalysts, relying on different activation modes. Before we stepped into this promising research field, there were already a few successful examples of asymmetric catalysis by utilizing chiral carbonyl compounds as catalysts. A pioneering example was the chiral ketone-catalyzed epoxidation of alkenes by forming a chiral dioxirane reagent in situ (Figure a). , Another successful example was documented by Beauchemin et al They reported the chiral aldehyde-catalyzed Cope-type hydroamination of allylic amines, where the chiral aldehydes acted as a catalytic temporary tether (Figure b). Moreover, Zhao et al reported chiral pyridoxals as catalysts to mimic biological transamination (Figure c, upper) …”
Section: Introductionmentioning
confidence: 99%
“…Carbonyl compounds typically serve as reagents in organic synthesis. However, they can also be used as catalysts, relying on different activation modes. Before we stepped into this promising research field, there were already a few successful examples of asymmetric catalysis by utilizing chiral carbonyl compounds as catalysts. A pioneering example was the chiral ketone-catalyzed epoxidation of alkenes by forming a chiral dioxirane reagent in situ (Figure a). , Another successful example was documented by Beauchemin et al They reported the chiral aldehyde-catalyzed Cope-type hydroamination of allylic amines, where the chiral aldehydes acted as a catalytic temporary tether (Figure b). Moreover, Zhao et al reported chiral pyridoxals as catalysts to mimic biological transamination (Figure c, upper) …”
Section: Introductionmentioning
confidence: 99%