Jianwei Yan

发表

Discovery of a low-systemic-exposure DGAT-1 inhibitor with a picolinoylpyrrolidine-2-carboxylic acid moiety.

Youhong Hu, Li-Fan Zeng, Bin Guo, 2017, Bioorganic & medicinal chemistry.

Direct synthesis of functional azaxanthones by using a domino three-component reaction.

Youhong Hu, Ming Cheng, Feng Hu, 2012, Organic letters.

Palladium-catalyzed cascade reactions of 3-iodochromones with aryl iodides and norbornadiene leading to annulated xanthones

Hong Chen, Youhong Hu, Ming Cheng, 2013 .

Gold-catalyzed reactions of 3-alkynyloxireno[2, 3-b]chromenones to form 3(2H)-furanones via a domino pathway.

Youhong Hu, Ming Cheng, Feng Hu, 2013, Chemistry, an Asian journal.

Au-catalyzed cascade addition/cyclization/H-transfer reactions of 3-(1-alkynyl)chromones to construct 4H-Furo[3,2-c]pyrans scaffold

Youhong Hu, Liping Huang, Taijie Chen, 2012 .

Synthesis and antitumor activity evaluation of lamiridosin A derivatives

Yan-Yan Yin, Fu‐Lin Yan, Jianwei Yan, 2016, Journal of Asian natural products research.

Synthesis and Anti-Tumour Activity Evaluation of Bergenin Derivatives

Yan-Yan Yin, Fu‐Lin Yan, Jianwei Yan, 2015 .

Simple and efficient procedures for selective preparation of 3-haloindoles and 2,3-dihaloindoles by using 1,3-dibromo-5,5-dimethylhydantoin and 1,3-dichloro-5,5-dimethylhydantoin

Fu‐Lin Yan, Ni Tianjun, Jianwei Yan, 2015 .

The dicarbonylation of indoles via Friedel–Crafts reaction with dicarbonyl nitrile generated in situ and retro-cyanohydrination

Guisheng Zhang, Guangjie He, Fu‐Lin Yan, 2016 .

Friedel–Crafts reaction of indoles with vicinal tricarbonyl compounds generated in situ from 1,3-dicarbonyl compounds and TEMPO: highly selective synthesis of tertiary alcohols

Fu‐Lin Yan, Ni Tianjun, Jixia Zhang, 2015 .

Indoles Oxidative Ring-Opening/Cyclization Cascade with the 1,2-Diaminoarenes: Direct Synthesis of 2-Aryl-3-(2-aminoaryl)quinoxalines.

Youhong Hu, Jianwei Yan, Linxia Zheng, 2022, The Journal of organic chemistry.

Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors.

Yong-tang Zheng, Shukun Li, Liu-meng Yang, 2012, Bioorganic & medicinal chemistry letters.

Highly efficient synthesis of quinoxaline derivatives from 1,2-benzenediamine and $$\alpha $$α-aminoxylated 1,3-dicarbonyl compounds

Yanhong Xu, Guisheng Zhang, Jie-Sheng Tian, 2016, Molecular Diversity.

Friedel-Crafts Reaction of Indoles with Vicinal Tricarbonyl Compounds Generated in situ from 1,3-Dicarbonyl Compounds and TEMPO: Highly Selective Synthesis of Tertiary Alcohols.

Fu‐Lin Yan, Ni Tianjun, Jixia Zhang, 2016 .

Direct synthesis of functional azaxanthones by using a domino three-component reaction.

Youhong Hu, Ming Cheng, Feng Hu, 2012, Organic Letters.