Lin Min
Wenzhou University
8 Papers
74 Citations
Lin Min is an academic researcher from Wenzhou University. The author has contributed to research in topics: Chemistry & Selenide. The author has an hindex of 4, co-authored 6 publications.
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Papers
Copper-Catalyzed Three-Component Coupling Reaction of Azoles, Se Powder, and Aryl Iodides
Gao Chao,Ge Wu,Lin Min,Miaochang Liu,Wenxia Gao,Jinchang Ding,Jiuxi Chen,Xiaobo Huang,Huayue Wu +8 more
TL;DR: A copper-catalyzed three-component coupling reaction of azoles, Se powder, and aryl iodide is described for the first time and provides a straightforward and facile pathway to synthesis 2-arylselanyl-azoles via a copper-Catalyzed double C-Se bonds formation process.
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Copper-Catalyzed Oxirane-Opening Reaction with Aryl Iodides and Se Powder.
TL;DR: Using Se powder as the selenating reagent, the copper-catalyzed double C-Se cross-coupling of aryl iodides, epoxides, and elemental selenium has been developed and it is shown that this process proceeds in generally good yields and is compatible with a broad range of functional groups.
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Metal-free synthesis of alkynyl alkyl selenides via three-component coupling of terminal alkynes, Se, and epoxides
TL;DR: A metal-free three-component coupling reaction of alkynes, Se powder and epoxides was described in this article, which provides an efficient and straightforward route for the preparation of alkynyl alkyl selenides via a double C-Se bond formation process.
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Patent
Synthetic method of Beta-hydroxyl selenide compound
Chen Jiuxi,Wu Huayue,Lin Min,Liu Miaochang,Gao Wenxia,Huang Xiaobo +5 more
- 25 Feb 2015
TL;DR: In this paper, a synthetic method for the synthesis of Beta-hydroxyl selenide compounds has been proposed, in which halogenated compound is used to react with elemental Se and epoxy compound to obtain Beta-Hydroxyl Selenide compound.
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Bischler-Napieralski Synthesis of Polycyclic N-Heteroaromatics Based on Tf2O-Promoted Electrophilic Activation of N-Aryl-2-Propynamides.
TL;DR: In this paper , a novel tandem synthesis of benzo[a]acridines is developed from N-aryl-2-propynamides and alkynes consisting of a Tf2O-promoted intermolecular Bischler-Napieralski reaction and a tfOH-promosed intramolecular Friedel-Crafts reaction.
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