Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Scott D, Kuduk"'
Autor:
Justin S. Cisar, Christine Pietsch, Lindsey G. DeRatt, Edgar Jacoby, Faraz Kazmi, Colleen Keohane, Katie Legenski, Rosalie Matico, Paul Shaffer, Yvan Simonnet, Alexandra Tanner, Chao-Yuan Wang, Weixue Wang, Ricardo Attar, James P. Edwards, Scott D. Kuduk
Publikováno v:
Journal of Medicinal Chemistry. 65:11241-11256
Autor:
Lindsey G. DeRatt, Bart Stoops, Paul Shaffer, Angela M. Lam, Christine Espiritu, Robert Vogel, Vincent Lau, Osvaldo A. Flores, Scott D. Kuduk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9be8563853e1080a3605e868030d58bb
https://doi.org/10.2139/ssrn.4437984
https://doi.org/10.2139/ssrn.4437984
Publikováno v:
The Journal of Organic Chemistry. 86:17482-17486
Herein, a tandem approach that allows rapid access to the benzomorpholine scaffold is reported. This operationally simple method allows for valuable heterocycles to be isolated in moderate to high yields. The overall transformation consists of an ini
Autor:
Scott D. Kuduk, Lindsey G. DeRatt, Bart Stoops, Paul Shaffer, Angela M. Lam, Christine Espiritu, Robert Vogel, Vincent Lau, Osvaldo A. Flores, George D. Hartman
Publikováno v:
Bioorganicmedicinal chemistry letters. 72
The HBV capsid core protein serves a number of important functions in the viral life cycle enabling chronic HBV infection to persist, and therefore is a promising drug target. Interfering with capsid assembly has shown efficacy in clinical trials wit
Autor:
Edward C. Lawson, Kiran Kumar, Renee L. DesJarlais, Soyon S Hwang, Scott D. Kuduk, Lindsey G. DeRatt
Publikováno v:
Organic Letters. 22:5828-5832
A tandem one-pot reaction featuring a cross-coupling followed by an intramolecular oxetane ring opening by mild nucleophiles is reported. The overall transformation comprises a carbon-carbon bond formation along with a carbon-heteroatom bond construc
Publikováno v:
Organic Letters. 21:9642-9645
Oxetanes have been increasingly used as stable motifs in medicinal chemistry as well as versatile synthetic intermediates. Herein, an intramolecular ring opening of oxetane carboxamides with mild nucleophiles, such as nitrogen heterocycles, is presen
Autor:
Scott D. Kuduk, Vincent Lau, Osvaldo Flores, Christine Espiritu, Robert Vogel, Angela M. Lam, George D. Hartman, Klaus Klumpp
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 29:2405-2409
The HBV core protein has multiple essential functions in the HBV life cycle to enable chronic HBV infection. The core protein oligomerizes to form the viral capsid, and modulation of the HBV capsid assembly process has shown clinical efficacy in earl
Autor:
Pamela L. Tannenbaum, Joanne eStevens, Jacquelyn eBinns, Alan eSavitz, Susan L Garson, Steven V Fox, Paul eColeman, Scott D Kuduk, Anthony L Gotter, Michael eMarino, Spencer J Tye, Jason eUslaner, Christopher J Winrow, John J Renger
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 8 (2014)
The ability to awaken from sleep in response to important stimuli is a critical feature of normal sleep, as is maintaining sleep continuity in the presence of irrelevant background noise. Dual orexin receptor antagonists (DORAs) effectively promote s
Externí odkaz:
https://doaj.org/article/bc2e2cdd06ec407c9158c769a6c72cea
Autor:
Andres D. Ramirez, Anthony L. Gotter, Steven V. Fox, Pamela L. Tannenbaum, Lihang eYao, Spencer J. Tye, Terrence eMcDonald, Joseph eBrunner, Susan L. Garson, Duane R. Reiss, Scott D. Kuduk, Paul J. Coleman, Jason M. Uslaner, Robert eHodgson, Susan E. Browne, John J. Renger, Christopher J. Winrow
Publikováno v:
Frontiers in Neuroscience, Vol 7 (2013)
Dual orexin receptor antagonists (DORAs) are a potential treatment for insomnia that function by blocking both the orexin 1 and orexin 2 receptors. The objective of the current study was to further confirm the impact of therapeutic mechanisms targeti
Externí odkaz:
https://doaj.org/article/7a637e4e89e342579deeac811d80cf1d
Publikováno v:
Organic letters. 22(19)
A convergent method for the rapid preparation of substituted isocoumarins is reported. The transformation takes advantage of a spontaneous intramolecular cyclization that follows the Pd-catalyzed α-arylation of aldehydes with 2-halobenzoic esters. T