1. Copper-catalyzed Peptide Synthesis from β-Amino Malononitrile and Amine using O2
Manuscript in preparation
Before XJTU (Selected publications)
1. Direct Cyclopropanation of α‐Cyano β‐Aryl Alkanes by Light‐Mediated Single Electron Transfer Between Donor-Acceptor Pairs.
Jing Li, Martin J. Lear, Yujiro Hayashi*
Chem. Eur. J. 2021, 27, 5901–5905.
Selected as Hot Paper.
2. A Chemoselective alpha-Oxytriflation Enables the Direct Asymmetric Arylation of Amides.
Jing Li, Martin Berger, Wojciech Zawodny, Marwan Simaan, Nuno Maulide*
Highlighted by Prof. Timothy R. Newhouse (Chem 2019, 5, 1687-1696)
Highlighted by (http://www.91hecheng.com/a/2098.html)
3. Enantioselective Redox-Neutral Coupling of Aldehydes and Alkenes by an Iron-Catalyzed "Catch-Release" Tethering Approach
Jing Li#, Alexander Preinfalk#, Nuno Maulide*
J. Am. Chem. Soc. 2019, 141, 143–147.
Highlighted by SYNFACTS (Synfact 2019, 15, 0385)
Highlighted by OPRD (Org. Process Res. Dev. 2019, 23, 674)
Highlighted by CHEMIE.DE (http://www.chemie.de/news/1160532/)
4. alpha-Arylation of Carbonyl Compounds via Oxidative C-C Bond Activation;
Jing Li, Adriano Bauer, Giovanni Di Mauro, Nuno Maulide*
Angew. Chem. Int. Ed. 2019, 58, 9816–9819.
Highlighted by X-MOL (https://www.x-mol.com/news/17811 and other academic websites)
5. Diastereo- and Enantioselective Access to Stereotriads through a Flexible Coupling of Substituted Aldehydes and Alkenes.
Jing Li#, Alexander Preinfalk#, and Nuno Maulide*
Angew. Chem. Int. Ed. 2019, 58, 5887–5890.
Highlighted by CHEMIE.DE (http://www.chemie.de/news/1160532/)
6. A Redox-Neutral Synthesis of Ketones by Coupling of Alkenes and Amides.
Jing Li#, Rik Oost#, Boris Maryasin, Leticia Gonzalez, Nuno Maulide*
7. Sterically Congested Ester Formation from alpha-Substituted Malononitrile and Alcohol via an Oxidative Method using Molecular Oxygen.
Yujiro Hayashi*, Jing Li, Hirotaka Asano, Daisuke Sakamoto
Eur. J. Org. Chem. 2019, 675–677.
8. Autoinductive conversion of alpha,alpha-diiodonitroalkanes to amides and esters catalysed by iodine byproducts under O2.
Jing Li, Martin J. Lear*, Yujiro Hayashi*
Chem. Commun. 2018, 54, 6360–6363.
9. Sterically Demanding Oxidative Amidation of alpha-Substituted Malononitriles with Amines using O2.
Jing Li, Martin J. Lear*, Yujiro Hayashi*
Angew. Chem. Int. Ed. 2016, 55, 9060–9064.
Highlighted by Organic Chemistry Portal Monday, May 22, 2017
10. Mechanism of Oxidative Amidation of Nitroalkanes with Oxygen and Amine Nucleophiles by Using Electrophilic Iodine.
Jing Li, Martin J. Lear, Eunsang Kwon, Yujiro Hayashi*
Chem. Eur. J. 2016, 22, 5538–5542.
11. Oxidative Amidation of Nitroalkanes with Amine Nucleophiles using Molecular Oxygen and Iodine.
Jing Li, Martin J. Lear, Yuya Kawamoto, Shigenobu Umemiya, Alice R. Wong, Eunsang Kwon, Itaru Sato, Yujiro Hayashi*
Angew. Chem. Int. Ed. 2015, 54, 12986–12990.
Highlighted by Organic Chemistry Portal Monday, May 23, 2016.
12. Chemoselective Activation of Diethyl Phosphonates: A Modular Synthesis of Biologically Relevant Phosphonylated Scaffolds.
C Pauline Adler, Amandine Pons, Jing Li, Joerg Heider, Bogdan R. Brutiu, Nuno Maulide*
Angew. Chem. Int. Ed. 2018, 57, 13330–13334.
13. Ynamide Preactivation Allows a Regio-and Stereoselective Synthesis of alpha, beta-disubstituted Enamides.
Lucas L. Baldassari, Aurelien de la Torre, Jing Li, Diogo S. Luedtke*, Nuno Maulide*
Angew. Chem. Int. Ed. 2017, 56, 15723–15727.
