Youwei Xie, Ph.D.
Affiliations: | Chemistry | University of Pittsburgh, Pittsburgh, PA, United States |
Area:
Reaction Design, Total Synthesis, Mechanistic Analysis, Diversity Oriented SynthesisGoogle:
"Youwei Xie"Mean distance: 8.43 | S | N | B | C | P |
Parents
Sign in to add mentorPaul E. Floreancig | grad student | 2014 | University of Pittsburgh | |
(Exploring the Synthetic Application of Allylic Alcohol Isomerization.) |
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Publications
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Zheng Y, Huang Q, Fang X, et al. (2024) Route to Functionalized Tetrahydrobenzo[]azepines via ReO-Mediated Intramolecular Friedel-Crafts Reaction. The Journal of Organic Chemistry |
Gul R, Hu L, Liu Y, et al. (2023) Synthesis of 1-Aryltetralins via ReO/HReO Mediated Intramolecular Hydroarylations. The Journal of Organic Chemistry. 88: 12079-12086 |
Liu H, Huang Q, Liao RZ, et al. (2023) Ring-closing C-O/C-O metathesis of ethers with primary aliphatic alcohols. Nature Communications. 14: 1883 |
Afeke C, Xie Y, Floreancig PE. (2019) ReO-Catalyzed Approach to Spirocyclic Ether Formation from Acyclic Precursors: Observation of Remote Stereoinduction. Organic Letters |
Qin Q, Xie Y, Floreancig PE. (2018) Diarylmethane synthesis through ReO-catalyzed bimolecular dehydrative Friedel-Crafts reactions. Chemical Science. 9: 8528-8534 |
Liu L, Kim H, Xie Y, et al. (2017) Catalytic Asymmetric [4+2]-Cycloaddition of Dienes with Aldehydes. Journal of the American Chemical Society |
Xie Y, List B. (2017) Catalytic Asymmetric Intramolecular [4+2] Cycloaddition of In Situ Generated ortho-Quinone Methides. Angewandte Chemie (International Ed. in English) |
Xie Y, Cheng GJ, Lee S, et al. (2016) Catalytic Asymmetric Vinylogous Prins Cyclization: A Highly Diastereo- and Enantioselective Entry to Tetrahydrofurans. Journal of the American Chemical Society |
Xie Y, Floreancig PE. (2014) Heterocycle synthesis based on allylic alcohol transposition using traceless trapping groups. Angewandte Chemie (International Ed. in English). 53: 4926-9 |
Xie Y, Floreancig PE. (2014) Heterocycle synthesis based on allylic alcohol transposition using traceless trapping groups Angewandte Chemie - International Edition. 53: 4926-4929 |