10.

Collective Synthesis of Chiral Tetrasubstituted Cyclobutanes Enabled by Enantioconvergent Negishi Cross-Coupling of Cyclobutenones
Min Yan+, Qiang Zhou+, and Ping Lu*

Angew. Chem. Int. Ed. 2023, 62, e202218008

9.

Dancing on Ropes Enantioselective Functionalization of Preformed Four M embered Carbocycles
Jun Chen, Qiang Zhou, Huayi Fang,* and Ping Lu*

Chin. J. Chem. 2022, 40, 13461358

8.

Enantioselective Construction of Vicinal Angular Quaternary Stereocenters Enabled by Strained Cyclobutenones
Peng Yan, Jia Zhang, Licheng Lu, Huayi Fang, and Ping Lu*

ACS Catal. 2022, 12, 15416−15423

7.

Diastereoselective synthesis of 1,1,3,3-tetrasubstituted cyclobutanes enabled by cycloaddition of bicyclo[1.1.0]butanes
Meng Wang, Yingchao Huang, Chunyu Li, and Ping Lu*

Org. Chem. Front., 2022, 9, 2149–2153

6.

Synthesis of Dibenzo[a,e]cyclooctene-5,11(6H,12H)-diones via the Elusive Benzocyclobutenone Anion
Yingchao Huang, Jun Chen, Yu Liu*, and Ping Lu*

Synthesis 2021, 53, 4477–4483.

5.

Enantioselective Synthesis of Indanes with a Quaternary Stereocenter via Diastereoselective C(sp3)−H Functionalization
Jun Chen, Zhan Shi, and Ping Lu*, 

Org. Lett. 2021, 23, 7359−7363.

4.

Enantioselective Functionalization of Prochiral Cyclobutanones and Cyclobutenones.

MengWang, Changxu Zhong, Ping Lu*,

Synlett, 2021, 32, 1253-1259.

2.

Chiral lithium amide mediated desymmetrization of 3-substituted cyclobutanone.

Changxu Zhong, Shaowei Wang and Ping Lu*,

Org. Chem. Front., 2021, 8, 2977-2980.

Graphical abstract: Chiral lithium amide mediated desymmetrization of 3-substituted cyclobutanone

 

 

1.

3-(Methoxycarbonyl)Cyclobutenone as a Reactive Dienophile in Enantioselective Diels–Alder Reactions Catalyzed by Chiral Oxazaborolidinium Ions,

Peng Yan, Changxu Zhong, Jie Zhang, Yu Liu, Huayi Fang, and Ping Lu*,

Angew. Chem. Int. Ed. 2021, 60, 4609-4613.