Jun Lin

发表

De Novo Design, Synthesis, and Biological Activities of High-Affinity and Selective Non-Peptide Agonists of the δ-Opioid Receptor‖

V. Hruby, H. Yamamura, F. Porreca, 1998 .

Desymmetrization and Switching of Stereoselectivity in Direct Organocatalytic Michael Addition of Ketones to 1,1‐Bis(phenylsulfonyl)ethylene

Kwunmin Chen, Y. Chen, Jun Lin, 2013 .

Asymmetric syntheses of highly hydrophobic chimeric aromatic amino acids: 2-Amino-3,3'-diarylpropionic acids

V. Hruby, S. Liao, Jun Lin, 1998 .

Synthesis and conformational features of topographically constrained designer chimeric amino acids: The β-isopropyl phenylalanines

V. Hruby, M. Shenderovich, S. Liao, 1997 .

Unraveling innate substrate-controlled arylation and bicyclization of 1,5-enynes with α,β conjugates: synthesis of substituted benzo[a]fluorenes

Jeh-Jeng Wang, B. Gore, Jun Lin, 2021 .

Asymmetric synthesis of all four isomers of topographically constrained novel amino acids: β-isopropyltyrosines

V. Hruby, Yinglin Han, W. Qiu, 1997 .

Synthesis of N-substituted 1,6-dihydro-3(2H)-pyridinones and 1-acyl-3-piperidones

Shihn‐Sheng Wu, E. Wang, Ling‐Ching Chen, 1984 .

Electrocatalytic synthesis of α,α-gem-dihalide ketones from α-mono-halide ketones and unexpected dimer condensation

G. Du, Lanxiang Liu, Tong Lin, 2022, Green Chemistry.

The stereochemical requirements of the novel δ-opioid selective dipeptide antagonist TMT-Tic

V. Hruby, H. Yamamura, F. Porreca, 1997 .