Jie An, Ph.D.

Affiliations: 
2019- Chemistry China Agricultural University, China 
Area:
Organic synthesis, New synthetic methods, Deuteration, Radical Chemistry
Website:
https://ajresearchgroup.com/
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"Jie An"
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Publications

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Wang L, Chen L, Qin Z, et al. (2023) Application of Iodine as a Catalyst in Aerobic Oxidations: A Sustainable Approach for Thiol Oxidations. Molecules (Basel, Switzerland). 28
Li H, Hou Y, Peng M, et al. (2023) Reductive Deuteration of Acyl Chlorides for the Synthesis of ,-Dideuterio Alcohols Using SmI and DO. Molecules (Basel, Switzerland). 28
Bisz E, Podchorodecka P, Li H, et al. (2022) Sequential Iron-Catalyzed C(sp)-C(sp) Cross-Coupling of Chlorobenzamides/Chemoselective Amide Reduction and Reductive Deuteration to Benzylic Alcohols. Molecules (Basel, Switzerland). 28
Han M, Ding Y, Yan Y, et al. (2018) Transition-Metal-Free, Selective Reductive Deuteration of Terminal Alkynes with Sodium Dispersions and EtOD- d. Organic Letters
Han M, Ma X, Yao S, et al. (2016) Development of a Modified Bouveault-Blanc Reduction for the Selective Synthesis of alpha,alpha-Dideuterio Alcohols. The Journal of Organic Chemistry
Fearnley AF, An J, Jackson M, et al. (2016) Synthesis of quaternary aryl phosphonium salts: photoredox-mediated phosphine arylation. Chemical Communications (Cambridge, England). 52: 4987-90
Fearnley AF, An J, Jackson M, et al. (2016) Synthesis of quaternary aryl phosphonium salts: Photoredox-mediated phosphine arylation Chemical Communications. 52: 4987-4990
Fearnley AF, An J, Jackson M, et al. (2016) ChemInform Abstract: Synthesis of Quaternary Aryl Phosphonium Salts: Photoredox-Mediated Phosphine Arylation. Cheminform. 47
An J, Work DN, Kenyon C, et al. (2014) Evaluating a sodium dispersion reagent for the Bouveault-Blanc reduction of esters. The Journal of Organic Chemistry. 79: 6743-7
An J, Denton RM, Lambert TH, et al. (2014) The development of catalytic nucleophilic substitution reactions: challenges, progress and future directions. Organic & Biomolecular Chemistry. 12: 2993-3003
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