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Yalan Xing
Researcher at William Paterson University
Publications - 78
Citations - 1302
Yalan Xing is an academic researcher from William Paterson University. The author has contributed to research in topics: Enantioselective synthesis & Cycloaddition. The author has an hindex of 16, co-authored 69 publications receiving 1025 citations. Previous affiliations of Yalan Xing include Chinese Academy of Sciences & Northeastern University.
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Recent Advances in Radical Difunctionalization of Simple Alkenes
TL;DR: A review of intermolecular and intramolecular radical difunctionalization of simple alkenes, with an emphasis on the reaction patterns and mechanisms, as well as potential applications in synthetic chemistry is given in this article.
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Copper/Manganese Cocatalyzed Oxidative Coupling of Vinylarenes with Ketones
TL;DR: A novel copper/manganese cocatalyzed direct oxidative coupling of terminal vinylarenes with ketones via C(sp(3))-H bond functionalization following C-C bond formation has been developed using tert-butyl hydroperoxide as the radical initiator.
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Organocatalytic and metal-mediated asymmetric [3 + 2] cycloaddition reactions
Yalan Xing,Nai-Xing Wang +1 more
TL;DR: In this paper, a review of recent progress in organocatalytic and metal-mediated asymmetric cycloadditions, including click chemistry, asymmetric 1,3-dipolar and asymmetric non-1,3dipolar, is presented.
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De Novo Asymmetric Synthesis of an α-6-Deoxyaltropyranoside as Well as its 2-/3-Deoxy and 2,3-Dideoxy Congeners
TL;DR: A highly divergent de novo asymmetric synthesis of benzyl alpha-6-deoxyaltropyranoside, benzylalpha-ascarylopyranosides, benzol alpha-amicetopyrnoside, and benzylAlpha-digitoxopyranuside has been achieved via a common pyranone intermediate.
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Unactivated C(sp3)–H Bond Functionalization of Alkyl Nitriles with Vinylarenes and Mechanistic Studies
TL;DR: The first example of a metal-free unactivated C(sp3)-H bond functionalization of alkyl nitriles with terminal vinylarenes to provide γ-ketonitrile derivatives is described and density functional theory (DFT) calculations provide important evidence of the free-radical pathway.