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David J Witter

Showing results (1-10 of 12) with videos related to

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The Journal of Organic Chemistry|April 19, 1996
Putative Diels-Alder-Catalyzed Cyclization during the Biosynthesis of LovastatinDavid J. Witter, John C. Vederas
The Journal of Organic Chemistry|June 22, 2010
A divergent approach to the synthesis of 3-substituted-2-pyrazolines: Suzuki cross-coupling of 3-sulfonyloxy-2-pyrazolinesJonathan B Grimm, Kevin J Wilson, David J Witter
The Journal of Organic Chemistry|September 21, 2007
A new strategy for the synthesis of benzylic sulfonamides: palladium-catalyzed arylation and sulfonamide metathesisJonathan B Grimm, Matthew H Katcher, David J Witter, et al.
Bioorganic & Medicinal Chemistry Letters|May 18, 2007
Aminosuberoyl hydroxamic acids (ASHAs): a potent new class of HDAC inhibitorsSandro Belvedere, David J Witter, Jiaming Yan, et al.
Bioorganic & Medicinal Chemistry Letters|June 20, 2007
Benzo[b]thiophene-based histone deacetylase inhibitorsDavid J Witter, Sandro Belvedere, Liqiang Chen, et al.
Bioorganic & Medicinal Chemistry Letters|December 7, 2007
Optimization of biaryl Selective HDAC1&2 Inhibitors (SHI-1:2)David J Witter, Paul Harrington, Kevin J Wilson, et al.
Bioorganic & Medicinal Chemistry Letters|June 9, 2007
Design of novel histone deacetylase inhibitorsPhieng Siliphaivanh, Paul Harrington, David J Witter, et al.
Bioorganic & Medicinal Chemistry Letters|February 29, 2008
Phenylglycine and phenylalanine derivatives as potent and selective HDAC1 inhibitors (SHI-1)Kevin J Wilson, David J Witter, Jonathan B Grimm, et al.
Bioorganic & Medicinal Chemistry Letters|March 10, 2009
Exploring the pharmacokinetic properties of phosphorus-containing selective HDAC 1 and 2 inhibitors (SHI-1:2)Richard W Heidebrecht, Melissa Chenard, Joshua Close, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 15, 2017
Evaluation of JAK3 Biology in Autoimmune Disease Using a Highly Selective, Irreversible JAK3 InhibitorFiona Elwood, David J Witter, Jennifer Piesvaux, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Journal of Organic Chemistry|April 19, 1996
Putative Diels-Alder-Catalyzed Cyclization during the Biosynthesis of LovastatinDavid J. Witter, John C. Vederas
The Journal of Organic Chemistry|June 22, 2010
A divergent approach to the synthesis of 3-substituted-2-pyrazolines: Suzuki cross-coupling of 3-sulfonyloxy-2-pyrazolinesJonathan B Grimm, Kevin J Wilson, David J Witter
The Journal of Organic Chemistry|September 21, 2007
A new strategy for the synthesis of benzylic sulfonamides: palladium-catalyzed arylation and sulfonamide metathesisJonathan B Grimm, Matthew H Katcher, David J Witter, et al.
Bioorganic & Medicinal Chemistry Letters|May 18, 2007
Aminosuberoyl hydroxamic acids (ASHAs): a potent new class of HDAC inhibitorsSandro Belvedere, David J Witter, Jiaming Yan, et al.
Bioorganic & Medicinal Chemistry Letters|June 20, 2007
Benzo[b]thiophene-based histone deacetylase inhibitorsDavid J Witter, Sandro Belvedere, Liqiang Chen, et al.
Bioorganic & Medicinal Chemistry Letters|December 7, 2007
Optimization of biaryl Selective HDAC1&2 Inhibitors (SHI-1:2)David J Witter, Paul Harrington, Kevin J Wilson, et al.
Bioorganic & Medicinal Chemistry Letters|June 9, 2007
Design of novel histone deacetylase inhibitorsPhieng Siliphaivanh, Paul Harrington, David J Witter, et al.
Bioorganic & Medicinal Chemistry Letters|February 29, 2008
Phenylglycine and phenylalanine derivatives as potent and selective HDAC1 inhibitors (SHI-1)Kevin J Wilson, David J Witter, Jonathan B Grimm, et al.
Bioorganic & Medicinal Chemistry Letters|March 10, 2009
Exploring the pharmacokinetic properties of phosphorus-containing selective HDAC 1 and 2 inhibitors (SHI-1:2)Richard W Heidebrecht, Melissa Chenard, Joshua Close, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 15, 2017
Evaluation of JAK3 Biology in Autoimmune Disease Using a Highly Selective, Irreversible JAK3 InhibitorFiona Elwood, David J Witter, Jennifer Piesvaux, et al.
Pageof 2