W. Chai

发表

The first potent and selective non-imidazole human histamine H4 receptor antagonists.

J. A. Jablonowski, Cheryl A. Grice, W. Chai, 2003, Journal of medicinal chemistry.

Non-imidazole heterocyclic histamine H3 receptor antagonists.

W. Chai, Annette K. Kwok, Sandy J. Wilson, 2003, Bioorganic & medicinal chemistry letters.

Synthesis of polyisoprene terpenoid dendrons and their applications in oligo(phenylene ethynylene)s as "shells".

W. Chai, Wei Wang, Zifa Shi, 2012, Chemistry, an Asian journal.

Solid phase synthesis of highly substituted 2,4-dioxopiperidines

W. Chai, W. Murray, 1999 .

REM sleep and in major depressive disorder

P. Bonaventure, W. Chai, C. Dvorak, 2012 .

Novel non-peptidic neuropeptide Y Y2 receptor antagonists.

P. Bonaventure, J. A. Jablonowski, W. Chai, 2004, Bioorganic & medicinal chemistry letters.

Switchable regioselectivity in lewis acid-promoted reactions of 1,4-benzoquinone monoimides with styrenyl systems: Selective syntheses of either 2-aryl-2,3-dihydrobenzofurans or 2-aryl-2,3-dihydroindoles

W. Chai, T. Engler, K. Lynch, 1995 .

Cycloaddition reactions of 1,4-benzoquinone mono- and bisimides with styrenyl systems: New syntheses of nitrogen substituted azapterocarpans, pterocarpans, 2-aryl-2,3-dihydroindoles and -dihydrobenzofurans

W. Chai, T. Engler, S. P. Meduna, 1995 .

Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues.

W. Chai, T. Engler, R. Iyengar, 1996, Bioorganic & medicinal chemistry.

Solution-phase combinatorial synthesis: Convergent multiplication of diversity via the olefin metathesis reaction

D. Boger, W. Chai, Wenying Chai, 1998 .

Synthesis of (±)-licarin B and eupomatenoids-1 and -12: A general approach to 2-aryl-7-alkoxy-benzofuranoid neolignans

W. Chai, T. Engler, 1996 .

A practical parallel synthesis of 2-substituted indolizines

W. Chai, Annette K. Kwok, N. Carruthers, 2003 .

Preparation and biological evaluation of indole, benzimidazole, and thienopyrrole piperazine carboxamides: potent human histamine h(4) antagonists.

J. A. Jablonowski, Cheryl A. Grice, W. Chai, 2005, Journal of medicinal chemistry.

Novel synthesis of amphiphilic dendrons by the double-stage convergent method.

W. Chai, Zifa Shi, Xiao-Ping Cao, 2009, Organic letters.

Reconsideration of 5-hydroxytryptamine (5-HT)(7) receptor distribution using [(3)H]5-carboxamidotryptamine and [(3)H]8-hydroxy-2-(di-n-propylamino)tetraline: analysis in brain of 5-HT(1A) knockout and 5-HT(1A/1B) double-knockout mice.

Xavier Langlois, Rene Hen, Pascal Bonaventure, 2002, The Journal of pharmacology and experimental therapeutics.

The discovery of potent selective NPY Y(2) antagonists.

P. Bonaventure, W. Chai, T. Lovenberg, 2013, Bioorganic & medicinal chemistry letters.

Solution-phase combinatorial synthesis via the olefin metathesis reaction

D. Boger, W. Chai, R. Ozer, 1997 .

Discovery of a Gut-Restricted JAK Inhibitor for the Treatment of Inflammatory Bowel Disease.

W. Chai, Jennifer D. Venable, J. Edwards, 2020, Journal of medicinal chemistry.