Xinxin Fang

China Pharmaceutical University — China

Chemistry · Physical Sciences

11h-index709citations16works0.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Catalytic C–H Functionalization Methods(11), Synthesis of Indole Derivatives(6), Oxidative Organic Chemistry Reactions(5), Asymmetric Synthesis and Catalysis(3), Catalytic Cross-Coupling Reactions(3)

Publications16 total

Palladium-Catalyzed Asymmetric Sequential Hydroamination of 1,3-Enynes: Enantioselective Syntheses of Chiral Imidazolidinones
Journal of the American Chemical Society·2022· 71 cited
Palladium-Catalyzed Remote 1,<i>n</i>-Arylamination of Unactivated Terminal Alkenes
ACS Catalysis·2019· 66 cited
Controllable Pd-Catalyzed Allylation of Indoles with Skipped Enynes: Divergent Synthesis of Indolenines and <i>N</i>-Allylindoles
Organic Letters·2018· 34 cited
Redox-Neutral Atom-Economic Pd(0)-Catalyzed Dearomatization of β-Naphthols with Alkynes toward Naphthalenones
Organic Letters·2018· 28 cited
Indium‐mediated Palladium‐catalyzed Allylic Alkylation of Isatins with Alkynes
Advanced Synthesis & Catalysis·2018· 15 cited
Photoredox Catalysis: Construction of Polyheterocycles via Alkoxycarbonylation/Addition/Cyclization Sequence
Organic Letters·2017· 112 cited
Addition of nitrogen dioxide to carbon–carbon double bond followed by a cyclization to construct nitromethylated isoquinolinediones
Organic & Biomolecular Chemistry·2017· 31 cited
Pd(<scp>ii</scp>)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones
Organic Chemistry Frontiers·2016· 32 cited
ChemInform Abstract: Palladium‐Catalyzed Dearomative Allylic Alkylation of Indoles with Alkynes to Synthesize Indolenines with C3‐Quarternary Centers.
ChemInform·2016
Palladium-Catalyzed Dearomative Allylic Alkylation of Indoles with Alkynes To Synthesize Indolenines with C3-Quarternary Centers
Organic Letters·2016· 66 cited
ChemInform Abstract: 1,6‐Conjugated Addition‐Mediated [2 + 1] Annulation: Approach to Spiro[2.5]octa‐4,7‐dien‐6‐one.
ChemInform·2016
ChemInform Abstract: Synthesis of Spiro[2.5]octa‐4,7‐dien‐6‐one with Consecutive Quaternary Centers via 1,6‐Conjugate Addition Induced Dearomatization of para‐Quinone Methides.
ChemInform·2016
Cu(<scp>i</scp>)-Catalyzed oxidative homo-coupling of thiazoline-4-carboxylates: synthesis of 4,4′-bithiazoline derivatives
Organic & Biomolecular Chemistry·2016· 3 cited
1,6-Conjugated Addition-Mediated [2+1] Annulation: Approach to Spiro[2.5]octa-4,7-dien-6-one
The Journal of Organic Chemistry·2015· 133 cited
Synthesis of spiro[2.5]octa-4,7-dien-6-one with consecutive quaternary centers <i>via</i> 1,6-conjugate addition induced dearomatization of <i>para</i>-quinone methides
Chemical Communications·2015· 118 cited
ChemInform Abstract: Convenient and Selective Synthesis of 4‐Trifluoromethylimidazoles.
ChemInform·1991

Frequent Co-authors

Hequan Yao(13), Aijun Lin(12), Zijun Wu(5), Xuanyi Li(4), Qiuyu Li(3), Shang Gao(3), Zhenbo Yuan(2), Jie Wu(2), Kuo Gai(2), Jinyi Xu(2), Jinhui Wu(2), Sheng‐Yi Zhuang(2), Peipei Sun(2), Xuanxuan Li(1), Ping Liu(1), Rui Pan(1), Chunhua Han(1), Zhiyuan Fu(1), Songjin Guo(1), Rui Shi(1)