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成果及论文

11. Enantioselective Total Synthesis of Bipolarolides A and B

Yufei Liu, † Ke Sun, † Qi Wei, † Jin Chen, Shengling Sun, Yaxin Li, Zhongkai Feng, Yingying Guo and Zhaohong Lu*  J. Am. Chem. Soc. 2025, 147,27219−27223

 


10. Total Synthesis of Paxdaphnine A and Daphlongamine B via an Aza-Prins Cyclization Strategy

Lu Ren, Zhaohong Lu, Dimin Wu, † Mingchen Ma, and Ang Li*  J. Am. Chem. Soc. 2025, 147, 27137−27142

9. Gram-Scale Total Synthesis of Illisimonin A

Liangchao Zhu, † Jinrui Li, † and Zhaohong Lu*  J. Am. Chem. Soc. 2025147, 23417−23421

8. Concise Total Synthesis of (−)-Bipolarolide D

Shengling Sun†, Qi Wei†, Yufei Liu, Zhaohong Lu*  J. Am. Chem. Soc. 2024, 146, 14427−14432.

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Before Independence


7. Microfluidic electrochemistry for single-electron transfer redox-neutral reactions

Yiming Mo , Zhaohong Lu , Girish Rughoobur , Prashant Patil , Neil Gershenfeld , Akintunde I Akinwande , Stephen L Buchwald , Klavs F Jensen*  Science 368, 1352–1357 (2020)


6. Enantioselective Preparation of Arenes with β-Stereogenic Centers: Confronting the 1,1-Disubstituted Olefin Problem Using CuH/Pd Cooperative Catalysis.

Zhaohong Lu , Stephen L Buchwald   Angew. Chem. Int. Ed. 2020, 59, 16128 – 16132


5. Total Synthesis of Aplysiasecosterol A

Zhaohong Lu , Xiang Zhang , Zhicong Guo , Yu Chen , Tong Mu , Ang Li  J. Am. Chem. Soc. 2018, 140, 9211−9218


4. Total Synthesis of Epoxyeujindole A

Zhaohong Lu , Hailong Li , Ming Bian , Ang Li  J. Am. Chem. Soc. 2015137, 13764−13767


3. Total Synthesis of Hapalindole-Type Natural Products

Zhaohong Lu , Ming Yang , Pengxi Chen , Xiaochun Xiong , Ang Li  Angew. Chem. 2014126, 14060 –14064


2. Mechanistically Guided Design of Ligands that Significantly Improve the Efficiency of CuH-Catalyzed Hydroamination Reactions

Andy A Thomas , Klaus Speck , Ilia Kevlishvili , Zhaohong Lu , Peng Liu , Stephen L Buchwald  J. Am. Chem. Soc. 2018, 140, 13976−13984


1. Total Syntheses of Aflavazole and 14-Hydroxyaflavinine

Hailong Li , Qifeng Chen , Zhaohong Lu , Ang Li  J. Am. Chem. Soc2016, 138, 15555−15558