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Lin Wang

Researcher at Yunnan University

Publications -  5
Citations -  81

Lin Wang is an academic researcher from Yunnan University. The author has contributed to research in topics: Cycloaddition & Catalysis. The author has an hindex of 3, co-authored 5 publications receiving 75 citations. Previous affiliations of Lin Wang include State Ethnic Affairs Commission.

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Rh-Catalyzed Highly Enantioselective Hydroalkynylation Reaction of Norbornadiene Derivatives

TL;DR: The complexes of various Rh precusors with ferrocenyl chiral ligand (R,S)-Cy2PF-PPh2 were found effective catalysts for the asymmetric hydroalkynylation reaction of norbornadiene derivatives.
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A study on the substituent effects of norbornadiene derivatives in iridium-catalyzed asymmetric [2 + 2] cycloaddition reactions

TL;DR: Employing a series of norbornadiene derivatives as substrates, the effects of various substituents on the Ir-catalyzed asymmetric [2 + 2] cycloaddition reactions with arylacetylenes were studied and it was found that the atom forming the short bridge chain had a great effect on the enantioselectivity of the reaction.
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Kinetic resolution of C1-substituted oxabenzonorbornadienes by Ir-catalyzed asymmetric [2+2] cycloaddition reactions with arylacetylenes

TL;DR: In this paper, the kinetic resolution of C1-substituted oxabenzonorbornadienes was realized by iridium-catalyzed asymmetric cycloaddition reaction with arylacetylenes.
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Kinetic Resolution of C1‐Substituted Oxabenzonorbornadienes by Ir‐Catalyzed Asymmetric [2 + 2] Cycloaddition Reactions with Arylacetylenes.

TL;DR: Cyclobutene cycloaddition products (III) and unreacted oxabenzonorbornadienes (I) are obtained with high to excellent enantiomeric excesses as discussed by the authors.
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A Study on the Substituent Effects of Norbornadiene Derivatives in Iridium‐Catalyzed Asymmetric [2 + 2] Cycloaddition Reactions.

TL;DR: In this article, the effects of various substituents on cycloaddition reactions with arylacetylenes were studied using a series of norbornadiene derivatives as substrates.