Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Donald R. Gauthier"'
Autor:
Anna Fryszkowska, Chihui An, Oscar Alvizo, Goutami Banerjee, Keith A. Canada, Yang Cao, Duane DeMong, Paul N. Devine, Da Duan, David M. Elgart, Iman Farasat, Donald R. Gauthier, Erin N. Guidry, Xiujuan Jia, Jongrock Kong, Nikki Kruse, Katrina W. Lexa, Alexey A. Makarov, Benjamin F. Mann, Erika M. Milczek, Vesna Mitchell, Jovana Nazor, Claudia Neri, Robert K. Orr, Peter Orth, Eric M. Phillips, James N. Riggins, Wes A. Schafer, Steven M. Silverman, Christopher A. Strulson, Nandhitha Subramanian, Rama Voladri, Hao Yang, Jie Yang, Xiang Yi, Xiyun Zhang, Wendy Zhong
Publikováno v:
Science (New York, N.Y.). 376(6599)
The emergence of new therapeutic modalities requires complementary tools for their efficient syntheses. Availability of methodologies for site-selective modification of biomolecules remains a long-standing challenge, given the inherent complexity and
Autor:
Marko Nesic, David B. Ryffel, Jonathan Maturano, Michael Shevlin, Scott R. Pollack, Donald R. Gauthier, Pablo Trigo-Mouriño, Li-Kang Zhang, Danielle M. Schultz, Jamie M. McCabe Dunn, Louis-Charles Campeau, Niki R. Patel, David A. Petrone, David Sarlah
The total synthesis of darobactin A, a recently isolated antibiotic that selectively targets Gram-negative bacteria, has been accomplished in a convergent fashion with a longest linear sequence of 16 steps from ᴅ-Garner’s aldehyde and ʟ-serine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85995d27bf0e6c17b4961bc72d2ca3c0
https://doi.org/10.26434/chemrxiv-2022-c4mz6
https://doi.org/10.26434/chemrxiv-2022-c4mz6
Publikováno v:
Organic letters. 24(17)
A highly efficient enantioselective synthesis for the potent G-protein-coupled receptor 40 agonist MK-2305 was developed. The key tetrasubstituted olefin was prepared via a stereoselective Mukaiyama aldol reaction/elimination sequence. The highly ena
Autor:
Ryan D. Cohen, Nadine Kuhl, Artis Klapars, Lauren Weisel, Susan L. Zultanski, Jamie M. McCabe Dunn, Jon A. Jurica, Anil R. Ekkati, Donald R. Gauthier, Mikhail Reibarkh, Wendy Zhong, Jungchul Kim
Publikováno v:
Organic Process Research & Development. 25:597-607
Cyclodextrin (CD) perfunctionalization reactions are challenging to study because they proceed through a number of regioisomeric intermediates, thus warranting creative approaches to understanding ...
Autor:
Zhixun Wang, Eric B. Sirota, Mark Weisel, John Y. L. Chung, Aaron M. Whittaker, Cyndi Qixin He, Donald R. Gauthier, François Lévesque, Danielle M. Schultz, Akasha K. Purohit, Yong-Li Zhong, Yingju Xu, Jonathan P. McMullen, Guy R. Humphrey, Varsolona Richard J, Cynthia M. Hong, Kevin M. Maloney
Publikováno v:
Organic Process Research & Development. 25:395-404
We report the practical synthesis of a key fragment of islatravir (MK-8591), a novel nucleoside reverse transcriptase translocation inhibitor (NRTTI) currently under investigation for treatment and...
Autor:
Andrew Brunskill, R. Thomas Williamson, Donald R. Gauthier, Mikhail Reibarkh, Yizhou Liu, Gary E. Martin, Yong-Li Zhong, Ikenna E. Ndukwe
Publikováno v:
Organic Letters. 21:4072-4076
Determining the configuration of proton-deficient molecules is challenging using conventional NMR methods including nuclear Overhauser effect (NOE) and the proton-dependent J-based configuration analysis (JBCA). The problem is exacerbated when only o
Autor:
Kevin M. Maloney, Guy R. Humphrey, Christopher A. Strulson, Hong Ren, Donald R. Gauthier, Guangtao Li, Rong Xiang
Publikováno v:
Green Chemistry. 19:4002-4006
The increasing employment of palladium-catalyzed reactions in the synthesis of active pharmaceutical ingredients (APIs) has created a pressing need for ultra-efficient palladium removal of the resulting metal contaminants. This communication discusse
Autor:
Roy Helmy, Yang Cao, Jinjian Zheng, Li-Kang Zhang, Huaming Sheng, Ross Yang, Donald R. Gauthier
Publikováno v:
Journal of Mass Spectrometry. 51:959-968
World Health Organization estimates that 34 million individuals globally are living with Human Immunodeficiency Virus (HIV). Doravirine is a non-nucleoside reverse transcriptase inhibitors (NNRTI) being evaluated by Merck for the treatment of HIV-1 i
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 59:386-390
An efficient synthesis for [(14) C]Omarigliptin (MK-3102) is described. The initial synthesis of a key (14) C-pyrazole moiety did not work due to the lack of stability of (14) C-DMF-DMA reagent. Thus, a new radiolabeled synthon, (14) C-biphenylmethyl
Autor:
Donald R. Gauthier, Naoki Yoshikawa
Publikováno v:
Organic letters. 18(23)
A simple and efficient method for converting methyl sulfones to sulfinic acids is described. The process involves alkylation with a benzylic halide, followed by in situ elimination of the resulting styrene in the presence of excess base to yield a su