C. McComas

发表

Total synthesis of the ristocetin aglycon.

D. Boger, B. Crowley, Y. Mori, 2004, Journal of the American Chemical Society.

Structure-dependent Impairment of Intracellular Apolipoprotein E4 Trafficking and Its Detrimental Effects Are Rescued by Small-molecule Structure Correctors*

Scott A. Peterson, R. Mahley, A. Meyer-Franke, 2011, The Journal of Biological Chemistry.

Synthesis and evaluation of methyl ether derivatives of the vancomycin, teicoplanin, and ristocetin aglycon methyl esters.

D. Boger, I. Hwang, B. Crowley, 2003, Bioorganic & medicinal chemistry letters.

Development of a New Structural Class of Broadly Acting HCV Non‐Nucleoside Inhibitors Leading to the Discovery of MK‐8876

A. Palani, M. Holloway, N. Liverton, 2017, ChemMedChem.

A general approach to access 5,6-dihydroindolo-naphthyridine ring system

Q. Dang, A. Palani, Peng Li, 2017 .

Design, synthesis, and SAR of new pyrrole-oxindole progesterone receptor modulators leading to 5-(7-fluoro-3,3-dimethyl-2-oxo-2,3-dihydro-1H-indol-5-yl)-1-methyl-1H-pyrrole-2-carbonitrile (WAY-255348).

R. Winneker, E. Melenski, Jeff Cohen, 2008, Journal of medicinal chemistry.

A new and improved method for deglycosidation of glycopeptide antibiotics exemplified with vancomycin, ristocetin, and ramoplanin.

D. Boger, Jutta Wanner, J. Moss, 2003, Bioorganic & medicinal chemistry letters.

A general approach to substituted 6H-pyrido[2′,3′:5,6] [1,3]oxazino[3,4-a]indole via cyclization from an indoline precursor followed by re-aromatization

Q. Dang, A. Palani, P. Li, 2013 .

Stereochemistry of 3-Alkylindole Dimerization: Acyclic δ1,δ1‘-Tryptophan Dimers

A. Gilbert, D. Vranken, C. McComas, 1997 .

Partitioning the loss in vancomycin binding affinity for D-Ala-D-Lac into lost H-bond and repulsive lone pair contributions.

Dale L Boger, D. Boger, Casey C McComas, 2003, Journal of the American Chemical Society.

Reduction of the indole ring system: synthesis of 4,5,6,7-tetrahydroindoles

D. Vranken, C. McComas, D. V. Vranken, 1999 .

Structure-activity relationships of norepinephrine reuptake inhibitors with benzothiadiazine dioxide or dihydrosulfostyril cores.

D. Deecher, E. Trybulski, G. Whiteside, 2010, Bioorganic & medicinal chemistry letters.

Synthesis of (+/-)-madindolines and chemical models. Studies of chemical reactivity.

D. V. Van Vranken, C. McComas, J. Perales, 2002, Organic letters.

Discovery of novel selective norepinephrine reuptake inhibitors: 4-[3-aryl-2,2-dioxido-2,1,3-benzothiadiazol-1(3H)-yl]-1-(methylamino)butan-2-ols (WYE-103231).

L. Leventhal, D. Deecher, E. Trybulski, 2010, Journal of medicinal chemistry.

Dianions and Tetraanions of Bowl‐Shaped Fullerene Fragments Dibenzo[a,g]corannulene and Dibenzo[a,g]cyclopenta[kl]corannulene

M. Rabinovitz, L. T. Scott, M. Bratcher, 1998 .

Synthesis and activity of novel 1- or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors.

E. Koury, D. Deecher, P. Mahaney, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and activity of 1-(3-amino-1-phenylpropyl)indolin-2-ones: a new class of selective norepinephrine reuptake inhibitors.

E. Koury, D. Deecher, P. Mahaney, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and activity of a new class of dual acting norepinephrine and serotonin reuptake inhibitors: 3-(1H-indol-1-yl)-3-arylpropan-1-amines.

L. Leventhal, P. Mahaney, E. Trybulski, 2006, Bioorganic & medicinal chemistry.

A new generation of progesterone receptor modulators

R. Winneker, C. McComas, M. Yudt, 2008, Steroids.

Novel progesterone receptor modulators: 4-aryl-phenylsulfonamides.

R. Winneker, E. Melenski, C. Huselton, 2012, Bioorganic & medicinal chemistry letters.

Application of chiral lithium amide bases to the thia-Sommelet dearomatization reaction

C. McComas, D. V. Vranken, 2003 .

Application of Chiral Lithium Amide Bases to the thia‐Sommelet Dearomatization Reaction.

C. McComas, D. V. Vranken, 2004 .

1- or 3-(3-Amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones: potent, selective, and orally efficacious norepinephrine reuptake inhibitors.

D. Deecher, P. Mahaney, E. Trybulski, 2009, Journal of medicinal chemistry.

Synthesis and activity of novel 1- or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors.

D. Deecher, P. Mahaney, E. Trybulski, 2008, Bioorganic & Medicinal Chemistry Letters.