王歆燕 博士，副研究员
Tel：86-10-62792789
Email：wangxinyan@tsinghua.edu.cn
教育背景
2000.9-2003.12 清华大学化学系 博士
1997.9-2000.7 中南大学化学系 硕士
1992.9-1996.7 中南大学化学系 本科
工作履历
2011.3-2012.3 美国麻省理工学院化学系 访问学者（Stephen. L. Buchwald教授课题组）
2011.1- 清华大学化学系 副研究员
2006.11-2010.12 清华大学化学系 助理研究员
2004.1-2006.10 清华大学化学系 博士后
研究领域
有机合成
不对称合成
含氮杂环的合成方法学研究
学术成果
代表性论文:
1. Li H, Shan L, Liu C, Liu N, Liu C, Wang X,* Hu, Y,* Chemospecific C3- and C2-Olefinations of Isatins by TfOH-Promoted Tandem Aldol-Grob and Semiacetalization-Grob Fragmentations, Organic Letters, 2023, 25, 4656-4660.
2. Shan L, Li H, Zheng W, Wang X, Wang X,* Hu, Y,* Tandem Synthesis of 2‑Azaspiro[4.5]deca-1,6,9-trien-8-ones Based on Tf2O‑Promoted Activation of N‑(2-Propyn-1-yl) Amides, Journal of Organic Chemistry, 2023, 88, 525-533.
3. Shan L, Li H, Zheng W, Wang X, Wang X,* Hu, Y,* Mechanistic Insights into Tf2O‑Promoted Electrophilic Activation of 2‑Propynamides and a New Synthesis of 2,4-Disubstituted Quinolines, Organic Letters, 2022, 24, 8806-8811.
4. Shan L, Weng Y, Li H, Min L, Wang X,* Hu, Y,* Bischler−Napieralski Synthesis of Polycyclic N‑Heteroaromatics Based on Tf2O‑Promoted Electrophilic Activation of N‑Aryl-2-Propynamides, Journal of Organic Chemistry, 2022, 87, 4124-4133.
5. Shan L, Li H, Min L, Weng Y, Wang X,* Hu, Y,* Bischler−Napieralski Synthesis of 6‑Alkynyl Phenanthridines Based on Tf2O‑Promoted Electrophilic Activation of N‑Aryl-2-propynamides, Journal of Organic Chemistry, 2021, 86, 15726-15732.
6. Li H, Shan L, Min L, Weng Y, Wang X,* Hu, Y,* Tandem Synthesis of 1,3-Disubstituted Naphthalenes via TfOH Promoted Directed-Aldol and Friedel−Crafts Reactions, Journal of Organic Chemistry, 2021, 86, 15011-15019.
7. Weng Y, Min L, Zeng X, Liu C, Shan L, Wang X,* Hu, Y,* General Synthesis of α‑Alkyl Ynones from Morpholine Amides and 1‑Copper(I) Alkynes Promoted by Triflic Anhydride, Organic Letters, 2020, 22, 8296-8301.
8. Luo D, Min L, Zheng W, Shan L, Wang X,* Hu, Y,* Introduction of N,N'-disulfonylhydrazines as new sulfonylating reagents for highly efficient synthesis of (E)-β-iodovinyl arenesulfones under mild conditions, Chinese Chemical Letters, 2020, 31, 1877-1880.
