Chen group

陈以昀课题组

Text Box: State Key Laboratory of Bioorganic and Natural Products Chemistry
Shanghai Institute of Organic Chemistry
Chinese Academy of Sciences

publications

18. Donor-Acceptor Complex Enables Alkoxyl Radical Generation for Metal-Free C(sp3)-C(sp3) Cleavage and Allylation/Alkenylation.  PDF

Zhang, J.; Li, Y.; Xu, R.; Chen, Y.*  Angew. Chem., Int. Ed. 2017, DOI: 10.1002/anie.201707171.

 

17. Selective Carbonyl-C(sp3) Bond Cleavage to Construct Ynamides, Ynoates, and Ynones by Photoredox Catalysis.  PDF

Jia, K.; Pan, Y.; Chen, Y.*  Angew. Chem., Int. Ed. 2017, 56, 2478 –2481. Highlighted by Chin. J. Org. Chem.

 

16. Visible-Light-Induced Carboxyl and Alkoxyl Radical Generations and Reactions.  PDF

Zhang, J.; Chen, Y.*  Acta Chim. Sin. 2017, 75, 41-48. Invited Review.

 

15. Polarity-Reversed Allylations of Aldehydes, Ketones, and Imines Enabled by Hantzsch Ester in Photoredox Catalysis.  PDF

Qi, L.; Chen, Y.*  Angew. Chem., Int. Ed. 2016, 55, 13312-13315.

 

14. Radical Decarboxylative Functionalizations Enabled by Dual Photoredox Catalysis.  PDF

Huang, H.1; Jia, K.1; Chen, Y.*  ACS Catal. 2016, 6, 4983-4988. Invited Perspective.

 

13. Visible-Light-Induced Alkoxyl Radical Generation Enables Selective C(sp3)-C(sp3) Bond Cleavage and Functionalizations.  PDF

Jia, K.; Zhang, F.; Huang, H.; Chen, Y.* J. Am. Chem. Soc. 2016, 138, 1514-1517. Highlighted by Organic Chemistry Portal and Organic Chemistry Highlights.

 

12. Generation  of Alkoxyl Radicals by Photoredox Catalysis Enables Selective C(sp3)-H Functionalization under Mild Reaction Conditions.  PDF

Zhang, J.; Li, Y.; Zhang, F.; Hu, C.; Chen, Y.* Angew. Chem., Int. Ed. 2016, 55, 1872-1875. Highlighted by Angew. Chem., Int. Ed.

 

11. Chemoselective and Fast Decarboxylative Allylation by Photoredox Catalysis under Mild Conditions.  PDF

Hu, C.; Chen, Y.* Org. Chem. Front. 2015, 2, 1352-1355.

 

10. Dual Hypervalent Iodine(III) Reagents and Photoredox Catalysis Enable Decarboxylative Ynonylation under Mild Conditions.  PDF

Huang, H.1; Zhang, G.1; Chen, Y.* Angew. Chem., Int. Ed. 2015, 54, 7872-7876. Highlighted by Chin. J. Org. Chem.

 

9. Biomolecule-Compatible Chemical Bond-Formation and Bond-Cleavage Reactions Induced by Visible Light.  PDF

Hu, C.; Chen, Y.* Tetrahedron Lett. 2015, 56, 884-888. Invited Digest.

 

8. Hypervalent Iodine Reagents Enable Chemoselective Deboronative/Decarboxylative Alkenylation by Photoredox Catalysis.  PDF

Huang, H.; Jia, K.; Chen, Y.* Angew. Chem., Int. Ed. 2015, 54, 1881-1884.

 

7. Visible-Light-Induced Chemoselective Reductive Decarboxylative Alkynylation under Biomolecule-Compatible Conditions.  PDF

Yang, J.; Zhang, J.; Qi, L.; Hu, C.; Chen, Y.* Chem. Comm. 2015, 51, 5275-5278. 2015 Emerging Investigator Issue.

 

6. Visible-Light-Induced Chemoselective Deboronative Alkynylation under Biomolecule-Compatible Conditions.  PDF

Huang, H.; Zhang, G.; Gong, L.; Zhang, S.; Chen, Y.* J. Am. Chem. Soc. 2014, 136, 2280-2283. Highlighted by Chin. J. Org. Chem., Organic Chemistry Portal, and Synfacts.

 

 

5. Discovery and Biological Characterization of Geranylated RNA in Bacteria.  PDF

Dumelin, C.E.; Chen, Y.; Leconte, A.M.; Chen, Y.G.; Liu, D.R. Nature Chem. Bio. 2012, 8, 913-919.

 

4. A Biomolecule-Compatible Visible-Light-Induced Azide Reduction from a DNA-Encoded Reaction-Discovery System.  PDF

Chen, Y.; Kamlet, A. S.; Steinman, J. B.; Liu, D. R., Nature Chem. 2011, 3, 146-153.

 

3. Ruthenium-Catalyzed Three-Component Coupling via Hydrative Conjugate Addition of Alkynes to Alkenes: One-Pot Synthesis of 1,4-Dicarbonyl Compounds.  PDF

Chen, Y.; Park, S. H.; Lee, C. W.; Lee, C.,  Chem. Asian J. 2011, 6, 2000-2004.

 

2. Tris(acetylacetonato)iron(III).  PDF

Chen, Y.; Lee, C., e-EROS Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; John Wiley & Sons, 2007.

 

1. Ruthenium-Catalyzed Hydrative Cyclization of 1,5-Enynes. PDF

Chen, Y.; Ho, D. M.; Lee, C.,  J. Am. Chem. Soc. 2005, 127, 12184-12185.

Chen group

陈以昀课题组

Text Box: State Key Laboratory of Bioorganic and Natural Products Chemistry
Shanghai Institute of Organic Chemistry
Chinese Academy of Sciences