Yong‐Jun Chen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Yong‐Jun Chen has a total of 15 co-authors. Here are the top co-authors by number of shared publications:
Dong Wang
Beijing National Laboratory for Molecular Science (BNLMS), CAS Key Laboratory for Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China), Fax: (+86) 10-6255-4449
4 shared publicationsZahid Shafiq
Beijing National Laboratory for Molecular Science (BNLMS), CAS Key Laboratory for Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China), Fax: (+86) 10-6255-4449
3 shared publicationsLi Liu
Center for Molecular Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China
2 shared publications- Li Liu
Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Molecular Recognition and Function, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
2 shared publications Qi‐Yu Zheng
Beijing National Laboratory for Molecular Science (BNLMS), CAS Key Laboratory for Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China), Fax: (+86) 10-6255-4449
2 shared publicationsZhen Qiao
Beijing National Laboratory for Molecular Science (BNLMS), CAS Key Laboratory for Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190 (China), Fax: (+86) 10-6255-4449
2 shared publications
Latest Publications
- 26 August 2010
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 49 (40) , 7294-7298
An Organocatalytic, δ‐Regioselective, and Highly Enantioselective Nucleophilic Substitution of Cyclic Morita–Baylis–Hillman Alcohols with Indoles
- 26 August 2010
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 49 (40) , 7294-7298
An Organocatalytic, δ‐Regioselective, and Highly Enantioselective Nucleophilic Substitution of Cyclic Morita–Baylis–Hillman Alcohols with Indoles
- 26 August 2010
- Published by Wiley in Angewandte Chemie
- Vol. 122 (40) , 7452-7456
An Organocatalytic, δ‐Regioselective, and Highly Enantioselective Nucleophilic Substitution of Cyclic Morita–Baylis–Hillman Alcohols with Indoles
- 26 August 2010
- Published by Wiley in Angewandte Chemie
- Vol. 122 (40) , 7452-7456
An Organocatalytic, δ‐Regioselective, and Highly Enantioselective Nucleophilic Substitution of Cyclic Morita–Baylis–Hillman Alcohols with Indoles
- 4 June 2007
- Published by Elsevier in Tetrahedron Letters
- Vol. 48 (23) , 3963-3967
Iodine-catalyzed allylation and propargylation of indoles with allylic and propargylic acetates
- 4 June 2007
- Published by Elsevier in Tetrahedron Letters
- Vol. 48 (23) , 3963-3967
Iodine-catalyzed allylation and propargylation of indoles with allylic and propargylic acetates
- 8 June 2006
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2006 (13) , 2977-2986
Asymmetric Mannich‐Type Reaction of a Chiral N‐(tert‐Butylsulfinyl) Ketimine with Imines: Application to the Synthesis of Chiral 1,3‐Diamines
Deprotonation of the chiral N‐(tert‐butylsulfinyl) ketimine 1 followed by trapping with imines 2 afforded the β‐aminoimines 3 as the Mannich‐type products in high diastereoselectivities (99:1 dr). As versatile synthons chiral β‐amino imines 3 could be transformed into enantiomeric β‐amino ketone and chiral syn‐ or anti‐1,3‐diamines with high diastereomeric excess by hydrolysis or reduction, respectively. Moreover, the nucleophilic addition of organometallicreagents to chiral β‐amino imines 3 could provide 1,1,3‐trisubstituted 1,3‐diamines with high diastereoselectivities. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
- 8 June 2006
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2006 (13) , 2977-2986
Asymmetric Mannich‐Type Reaction of a Chiral N‐(tert‐Butylsulfinyl) Ketimine with Imines: Application to the Synthesis of Chiral 1,3‐Diamines
Deprotonation of the chiral N‐(tert‐butylsulfinyl) ketimine 1 followed by trapping with imines 2 afforded the β‐aminoimines 3 as the Mannich‐type products in high diastereoselectivities (99:1 dr). As versatile synthons chiral β‐amino imines 3 could be transformed into enantiomeric β‐amino ketone and chiral syn‐ or anti‐1,3‐diamines with high diastereomeric excess by hydrolysis or reduction, respectively. Moreover, the nucleophilic addition of organometallicreagents to chiral β‐amino imines 3 could provide 1,1,3‐trisubstituted 1,3‐diamines with high diastereoselectivities. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
- 16 December 2005
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 2006 (1) , 0096-0100
Three-Component Friedel-Crafts Reaction of Indoles, Glyoxylate, and Amine under Solvent-Free and Catalyst-Free Conditions - Synthesis of (3-Indolyl)glycine Derivatives
Solvent-free and catalyst-free three-component reactions of indoles, amines, and ethyl glyoxylate gave alkylation products in good to high yields (61-93%), providing a convenient synthesis of (3-indolyl)glycine derivatives.
- 16 December 2005
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 2006 (1) , 0096-0100
Three-Component Friedel-Crafts Reaction of Indoles, Glyoxylate, and Amine under Solvent-Free and Catalyst-Free Conditions - Synthesis of (3-Indolyl)glycine Derivatives
Solvent-free and catalyst-free three-component reactions of indoles, amines, and ethyl glyoxylate gave alkylation products in good to high yields (61-93%), providing a convenient synthesis of (3-indolyl)glycine derivatives.