An-Hu Li

发表

Asymmetric Ylide Reactions: Epoxidation, Cyclopropanation, Aziridination, Olefination, and Rearrangement.

V. Aggarwal, L. Dai, An-Hu Li, 1997, Chemical reviews.

Discovery of 2-Amino-3-amido-5-aryl-pyridines as Highly Potent, Orally Bioavailable, and Efficacious PERK Kinase Inhibitors.

Jennifer R. Wolfley, M. Koszelak-Rosenblum, A. C. Rigby, 2021, Bioorganic & medicinal chemistry letters.

Discovery of an Orally Efficacious Imidazo[5,1-f][1,2,4]triazine Dual Inhibitor of IGF-1R and IR.

D. Werner, P. Gokhale, E. May, 2010, ACS medicinal chemistry letters.

Aziridination of N-sulfonylimines with a stabilized sulfonium ylide: simple preparation of N-sulfonyl-2-[(E)-2-(alkoxycarbonyl)ethenyl]-3-arylaziridines

X. Hou, L. Dai, An-Hu Li, 1996 .

Pyran template approach to the design of novel A3 adenosine receptor antagonists

K. Jacobson, X. Ji, N. Melman, 1999, Drug development research.

Optimization of a Novel Mandelamide-Derived Pyrrolopyrimidine Series of PERK Inhibitors

A. C. Rigby, M. Betzenhauser, Michael E. Stokes, 2022, Pharmaceutics.

Asymmetric Aziridination over Ylides: Highly Stereoselective Synthesis of Acetylenyl‐N‐sulfonylaziridines

Lin Lin, Yong‐Gui Zhou, X. Hou, 1997 .

Dihydropyridines as inhibitors of capacitative calcium entry in leukemic HL-60 cells.

K. Jacobson, J. Daly, J. Harper, 2003, Biochemical pharmacology.

Polymethylhydrosiloxane (PMHS)/trifluoroacetic acid (TFA): a novel system for reductive amination reactions

Hanqing Dong, V. Korlipara, M. Mulvihill, 2009 .

A highly effective one-pot synthesis of quinolines from o-nitroarylcarbaldehydes.

M. Cox, Qinghua Weng, D. Werner, 2007, Organic & biomolecular chemistry.

Preparation of Enantiomerically Enriched (2R,3R)- or (2S,3S)-trans-2,3-Diaryloxiranes via Camphor-Derived Sulfonium Ylides.

Feng-Wei Li, X. Hou, L. Dai, 1996, The Journal of organic chemistry.

One-Pot FriedländerQuinoline Synthesis: Scope and Limitations

D. Werner, A. Crew, Kam W. Siu, 2010 .

The first efficient preparation of vinylaziridines via an ylide route

X. Hou, L. Dai, An-Hu Li, 1996 .

The Aziridination of N-Tosylimines with Amide-Stabilized Sulfonium Ylides: A Simple and Efficient Preparation of Aziridinyl Carboxamides

Yong‐Gui Zhou, X. Hou, L. Dai, 1997 .

Efficient Synthesis of p-Sulfonic Acid Calixarene under Ultrasonic Irradiation

An-Hu Li, 2014 .

A Direct Route to C-Vinylaziridines: Reaction of N-Sufonylimines with Allylic Ylides under Phase-Transfer Conditions or with Preformed Ylides at Low Temperature.

Min-Bo Chen, X. Hou, L. Dai, 1996, The Journal of organic chemistry.

Facile preparation of vinylaziridines by the reaction of N-sulfonylimines and cinnamyl bromide mediated by a catalytic amount of dimethyl sulfide

X. Hou, L. Dai, An-Hu Li, 1996 .

A straight synthesis of 2–(α-substituted N-tosylaminomethyl)-2,5-dihydrofurans by the reaction of N-sulfonylimines with arsonium 4-hydroxyl- cis -2-butenylides

W. Deng, X. Hou, L. Dai, 2010 .

Stereocontrolled synthesis of either trans- or cis-trimethylsilylvinyloxiranes via sulfonium ylides

Yong‐Gui Zhou, X. Hou, L. Dai, 1996 .

OSI-930: a novel selective inhibitor of Kit and kinase insert domain receptor tyrosine kinases with antitumor activity in mouse xenograft models.

G. Wynne, N. Gibson, D. Emerson, 2006, Cancer research.

A3 adenosine receptors: Protective vs. damaging effects identified using novel agonists and antagonists

S. Moro, K. Jacobson, Yong‐Chul Kim, 1998, Drug development research.

Discovery and optimization of 7-aminofuro[2,3-c]pyridine inhibitors of TAK1.

James G. Tarrant, M. Albertella, D. Berger, 2013, Bioorganic & medicinal chemistry letters.

Novel 6-aminofuro[3,2-c]pyridines as potent, orally efficacious inhibitors of cMET and RON kinases.

M. Albertella, P. Gokhale, D. Epstein, 2013, Bioorganic & medicinal chemistry letters.

Molecular Modeling Studies of Human A3 Adenosine Antagonists: Structural Homology and Receptor Docking

S. Moro, K. Jacobson, An-Hu Li, 1998, J. Chem. Inf. Comput. Sci..

Structure-activity relationships and molecular modeling of 3, 5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists.

S. Moro, K. Jacobson, X. Ji, 1998, Journal of medicinal chemistry.

Functionalized congeners of 1,4-dihydropyridines as antagonist molecular probes for A3 adenosine receptors.

K. Jacobson, X. Ji, N. Melman, 1999, Bioconjugate chemistry.

Synthesis of 2-(α-Substituted N-Tosylaminomethyl)-2,5-Dihydrofurans by Reaction of N-Sulfonylimines with Arsonium or Sulfonium 4-Hydroxyl-cis-2-butenylides

X. Hou, L. Dai, An-Hu Li, 2000 .

Synthesis of 2-(α-Substituted N-Tosylaminomethyl)-2,5-dihydrofurans by Reaction of N-Sulfonylimines with Arsonium or Sulfonium 4-Hydroxy-cis-2-butenylides.

X. Hou, L. Dai, An-Hu Li, 2000 .