(Highlighted by Synfacts 2022, 18, 1204.; Highlighted by X-MOL)
Zhi-Heng Li§, Dan-Ran Li§, Hua-Ming Xiang, Jian Huang, Yi-Nuo Zheng(本科生), Cuiju Zhu, Xiuling Cui, Chao Pi*, and Hao Xu*
Chinese Chem. Lett. 2022, 33 , 867–870.
Chem. Comm. 2021, 57, 4674–4677. (This article is part of the themed collection: 2021 Emerging Investigators)
Julian Wilke, Tatsuro Kawamura, Hao Xu, Alexandra Brause, Alexandra Friese, Malte Metz, Dirk Schepmann, Bernhard Wünsch, Antonia Artacho-Cordón, Francisco R.Nieto, Nobumoto Watanabe, Hiroyuki Osada, Slava Ziegler, Herbert Waldmann*
Cell Chem. Biol. 2021, 28, 848–854.
Si-Jia Li§, Jian Huang§, Jin-Yu He, Rui-Jin Zhang, Hao-Dong Qian, Xue-Lin Dai (本科生), Han-Han Kong and Hao Xu*
RSC Adv. 2020, 10, 38478.
A highly enantioselective copper-catalyzed propargylic amination starting from benzylic allylic amines has been developed with a new chiral N,N,P ligand, providing a series of N-tethered 1,6-enynes in good to excellent yields with excellent enantioselectivities.
Hao Xu, Luca Laraia, Laura Schneider, Kathrin Louven, Carsten Strohmann, Andrey P. Antonchick* and Herbert Waldmann*;
Angew. Chem. Int. Ed. 2017, 56, 11232.
(Highlighted by Synfacts. 2017, 13, 1047.)
Hao Xu, Christopher Golz, Carsten Strohmann, Andrey P. Antonchick* and Herbert Waldmann*;
Angew. Chem. Int. Ed. 2016, 55, 7761.
Hao Xu§, Jiang-Lin Hu§, Li-Jia Wang, Sai-Hu Liao and Yong Tang*;
Asymmetric Annulation of Donor−Acceptor Cyclopropanes with Dienes. (§: contributed equally)
J. Am. Chem. Soc. 2015, 137, 8006.
(Highlighted by Synfacts. 2015, 11, 956.)
Jiang-Lin Hu, Li-Jia Wang, Hao Xu, Zuo-Wei Xie* and Yong Tang*;
Org. Lett. 2015, 17, 2680.
Hao Xu§, Jian-Ping Qu§, Sai-Hu Liao, Hu Xiong and Yong Tang*;
Angew. Chem. Int. Ed. 2013, 52, 4004. (Selected as a Hot paper)
(Highlighted by Synfacts. 2013, 9, 648.)
Hu Xiong§, Hao Xu§, Sai-Hu Liao, Zuo-Wei Xie* and Yong Tang*;
( §: contributed equally)
(Highlighted by Synform, 2013, 7, 122.)
|Congratulations to Zi-Qi Geng and Chunhui Zhao whose paper on "Cu/Ag-Mediated One-Pot Enantioselective Synthesis of FullyDecorated 1,2,3-Triazolo[1,5‑a]pyrazines" has been publised in "Org. Lett.".|