6 Papers
Da Li is an academic researcher from Zhejiang Sci-Tech University. The author has contributed to research in topics: Catalysis & Aryl. The author has an hindex of 6, co-authored 6 publications.
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Papers
Palladium-Catalyzed Carbonylative Synthesis of α,β-Unsaturated Amides from Styrenes and Nitroarenes.
TL;DR: A procedure on palladium-catalyzed selective aminocarbonylation of styrenes with nitroarenes for the synthesis of α, β-unsaturated amides has been developed and a range of substituted α,β-uns saturated amides were synthesized in moderate to good yields.
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Palladium-Catalyzed Amide Synthesis via Aminocarbonylation of Arylboronic Acids with Nitroarenes.
TL;DR: A palladium-catalyzed aminocarbonylation of aryl boronic acids with nitroarenes with a wide range of substrates provided a redox-economical process for the synthesis of amides and gave the corresponding amides in moderate to good yields.
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Selectivity controllable divergent synthesis of α,β-unsaturated amides and maleimides from alkynes and nitroarenes via palladium-catalyzed carbonylation
TL;DR: In this paper, a tunable procedure on palladium-catalyzed carbonylative divergent synthesis of α, β -unsaturated amides and maleimides from symmetrical internal alkynes and nitroarenes has been developed.
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Carbonylative Transformation of Allylarenes with CO Surrogates: Tunable Synthesis of 4-Arylbutanoic Acids, 2-Arylbutanoic Acids, and 4-Arylbutanals.
TL;DR: In this Communication, procedures for the selective synthesis of 4-arylbutanoic acids, 2-aryl Butanals, and 4- Darylbutanals from the same allylbenzenes have been developed with formic acid or TFBen as the CO surrogate, reactions proceed selectively and effectively under carbon monoxide gas-free conditions.
Palladium-Catalyzed Regioselective Carbonylative Coupling/Amination of Aryl Iodides with Unactivated Alkenes: Efficient Synthesis of β-Aminoketones
TL;DR: In this article, a palladium-cata... is used for the carbonylative coupling of aryl halides with unactivated alkenes, which is a challenge because of the low reactivity of acyl-palladium intermediate to the olefins.