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Youwei Xie, Ph.D.

Affiliations: 
Chemistry University of Pittsburgh, Pittsburgh, PA, United States 
Area:
Reaction Design, Total Synthesis, Mechanistic Analysis, Diversity Oriented Synthesis
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"Youwei Xie"
Mean distance: 8.43
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Parents

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Paul 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
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