Han-Qing Dong

发表

Diverse synthesis of marine cyclic depsipeptide lagunamide A and its analogues.

Bangguo Wei, G. Lin, Rong‐Guo Ren, 2013, The Journal of organic chemistry.

A useful synthesis of the Phe-Arg phosphinic acid dipeptide isostere

F. H. Ebetino, A. Kende, Han-Qing Dong, 2002 .

Highly Enantioselective Rhodium-Catalyzed Cross-Addition of Silylacetylenes to Cyclohexadienone-Tethered Internal Alkynes.

G. Lin, Han-Qing Dong, Jun-Li Zhang, 2019, Organic letters.

Recent applications of chiral N-tert-butanesulfinyl imines, chiral diene ligands and chiral sulfur–olefin ligands in asymmetric synthesis

G. Lin, Han-Qing Dong, Ming‐Hua Xu, 2015 .

Divergent Synthesis of Revised Apratoxin E, 30-epi-Apratoxin E, and 30S/30R-Oxoapratoxin E.

Zhuo-Ya Mao, Changmei Si, Bangguo Wei, 2017, The Journal of organic chemistry.

Asymmetric Synthesis of Apratoxin E.

Zhuo-Ya Mao, Changmei Si, Bangguo Wei, 2016, The Journal of organic chemistry.

Divergent Method to trans-5-Hydroxy-6-alkynyl/alkenyl-2-piperidinones: Syntheses of (-)-Epiquinamide and (+)-Swainsonine.

Zhuo-Ya Mao, Changmei Si, Bangguo Wei, 2015, The Journal of organic chemistry.

Rhodium-Catalyzed Asymmetric Arylation

G. Lin, Han-Qing Dong, Ping Tian, 2012 .

One-pot enantioselective construction of indoloquinolizidine derivatives bearing five contiguous stereocenters using aliphatic aldehydes, nitroethylenes, and tryptamine.

G. Lin, Hua-Chen Lin, Han-Qing Dong, 2014, Chemical communications.

Aryl-indolyl maleimides as inhibitors of CaMKIIdelta. Part 1: SAR of the aryl region.

J. Higaki, Yong-jin Xu, B. Mavunkel, 2008, Bioorganic & medicinal chemistry letters.

Radical migration-addition of N-tert-butanesulfinyl imines with organozinc reagents.

Bangguo Wei, Jian-Liang Ye, Wei Huang, 2013, The Journal of organic chemistry.

New heterocyclic structures from unsaturated aldehyde derivatives. Inhibition of α-L-fucosidases

W. Frey, Han-Qing Dong, V. Jäger, 2000 .

Sc(OTf)3-catalyzed intramolecular diastereoselective cyclization from tert-butoxycarbonyl to acyliminium ion

X. Nie, Zhuo-Ya Mao, Changmei Si, 2021 .

Enantioselective Total Syntheses and Stereochemical Studies of All Four Stereoisomers of Yingzhaosu C

Xingxiang Xu, Han-Qing Dong, 1995 .

Copper-catalyzed asymmetric hydroboration of α-dehydroamino acid derivatives: facile synthesis of chiral β-hydroxy-α-amino acids.

G. Lin, Chuan‐Chuan Wang, Zhiheng He, 2014, Organic letters.

Preparation of ‘carba’ dipeptides bearing a basic side-chain at the C-terminus: synthesis of enantiopure Boc-d-Phe-Ψ[CH2CH2]-l-Arg(NO2)-OH and Boc-d-Phe-Ψ[CH2CH2]-d-Arg(NO2)-OH

A. Mazur, F. H. Ebetino, A. Kende, 2001 .

Practical Asymmetric Synthesis of Amathaspiramides B, D, and F.

G. Lin, Han-Qing Dong, Xingwen Sun, 2016, Organic letters.

Vitamin B12 Catalysis of Zinc‐Mediated 6‐Deoxy‐6‐iodopyranoside Fragmentation: A Mild and Convenient Preparation of ω‐Unsaturated Hexose Derivatives (5‐Hexenoses).

Han-Qing Dong, P. Hilgers, M. Kleban, 2000 .

Aryl-indolyl maleimides as inhibitors of CaMKIIdelta. Part 2: SAR of the amine tether.

J. Higaki, Yong-jin Xu, B. Mavunkel, 2008, Bioorganic & medicinal chemistry letters.

Aryl-indolyl maleimides as inhibitors of CaMKIIdelta. Part 3: Importance of the indole orientation.

S. Sideris, J. Higaki, Yong-jin Xu, 2008, Bioorganic & medicinal chemistry letters.

One-pot enantioselective construction of indoloquinolizidine derivatives bearing five contiguous stereocenters using aliphatic aldehydes, nitroethylenes, and tryptamine.

G. Lin, Hua-Chen Lin, Han-Qing Dong, 2014, Chemical communications.