8 Papers
33 Citations
Bing Jiang is an academic researcher from University of Science and Technology of China. The author has contributed to research in topics: Catalysis & Lewis acids and bases. The author has an hindex of 7, co-authored 8 publications.
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Papers
Chelation versus Non-Chelation Control in the Stereoselective Alkenyl sp2 C−H Bond Functionalization Reaction
Qiu-Ju Liang,Chao Yang,Fei-Fan Meng,Bing Jiang,Yun-He Xu,Teck-Peng Loh,Teck-Peng Loh,Teck-Peng Loh +7 more
TL;DR: A hydroxy group chelation-assisted stereospecific oxidative cross-coupling reaction between alkenes was developed under mild reaction conditions, acting as the directing group for alkenyl C-H bond activation and controlling the stereoselectivity of the products.
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B(C6F5)3: A New Class of Strong and Bulky Lewis Acid for Exo-Selective Intermolecular Diels–Alder Reactions of Unreactive Acyclic Dienes with α,β-Enals
TL;DR: The substituent effect of the dienes and dienophiles on the product's stereoselectivity was thoroughly investigated, and it was found that most of the desired ex-Diels-Alder products could be obtained in good yields and with high exo-stereoselectivities.
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Palladium-Catalyzed Direct Intramolecular C-N Bond Formation: Access to Multisubstituted Dihydropyrroles.
TL;DR: A palladium-catalyzed intramolecular amination of alkenes with retention of olefin functionalization was achieved under mild reaction conditions and the tosyl-protected amine can directly couple with a double bond to provide versatile dihydropyrrole derivatives in moderate to excellent yields.
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Copper-Catalyzed Dehydrogenative Diels–Alder Reaction
Bing Jiang,Qiu-Ju Liang,Yu Han,Meng Zhao,Yun-He Xu,Teck-Peng Loh,Teck-Peng Loh,Teck-Peng Loh +7 more
TL;DR: A practical and effective copper-catalyzed dehydrogenative Diels-Alder reaction of gem-diesters and ketone with dienes with good to excellent yields of polysubstituted cyclohexene derivatives is established.
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Divergent Protosilylation and Protoborylation of Polar Enynes
Fei-Fan Meng,Qi-Yan Xue,Bing Jiang,Meng Zhao,Jia-Hao Xie,Yun-He Xu,Teck-Peng Loh,Teck-Peng Loh +7 more
TL;DR: Novel cascade double protoborylation/protodeboronation processes of polar enynoates enabled access of the useful trisubstituted vinylboronates in up to 80% yield and with up to 98:2 Z/ E ratio.
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