Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Byron K. Peters"'
Autor:
Nakita Reddy, Letisha Girdhari, Mbongeni Shungube, Arnoldus C. Gouws, Byron K. Peters, Kamal K. Rajbongshi, Sooraj Baijnath, Sipho Mdanda, Thandokuhle Ntombela, Thilona Arumugam, Linda A. Bester, Sanil D. Singh, Anil Chuturgoon, Per I. Arvidsson, Glenn E. M Maguire, Hendrik G. Kruger, Thavendran Govender, Tricia Naicker
Publikováno v:
Antibiotics, Vol 12, Iss 4, p 633 (2023)
Virulent Enterobacterale strains expressing serine and metallo-β-lactamases (MBL) genes have emerged responsible for conferring resistance to hard-to-treat infectious diseases. One strategy that exists is to develop β-lactamase inhibitors to counte
Externí odkaz:
https://doaj.org/article/72015b20994f46ae9bddd7b2baa61e04
Autor:
Min Zhou, Jet Tsien, Ryan Dykstra, Jonathan M. E. Hughes, Byron K. Peters, Rohan R. Merchant, Osvaldo Gutierrez, Tian Qin
Publikováno v:
Nature Chemistry. 15:550-559
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41c25e5adc5e48fe671cf32ecbba01e7
https://doi.org/10.1038/s41557-023-01150-z
https://doi.org/10.1038/s41557-023-01150-z
Autor:
Byron K. Peters, Nakita Reddy, Mbongeni Shungube, Letisha Girdhari, Sooraj Baijnath, Sipho Mdanda, Lloyd Chetty, Thandokuhle Ntombela, Thilona Arumugam, Linda A. Bester, Sanil D. Singh, Anil Chuturgoon, Per I. Arvidsson, Glenn E. M. Maguire, Hendrik G. Kruger, Tricia Naicker, Thavendran Govender
Publikováno v:
ACS Infectious Diseases. 9:486-496
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fa25a0f93d4b4812b6db1bfae888f81
https://doi.org/10.1021/acsinfecdis.2c00485
https://doi.org/10.1021/acsinfecdis.2c00485
Autor:
Chao Hu, Cuong Vo, Rohan R. Merchant, Si-Jie Chen, Jonathan M. E. Hughes, Byron K. Peters, Tian Qin
Publikováno v:
J Am Chem Soc
Heterocycles are the backbone of modern medical chemistry and drug development. The derivatization of "an olefin" inside aromatic rings represents an ideal approach to access functionalized saturated heterocycles from abundant aromatic building block
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb786bc1df463228da2a87e6e6ebb65
https://doi.org/10.1021/jacs.2c11664
https://doi.org/10.1021/jacs.2c11664
Publikováno v:
Nature Chemistry. 13:950-955
Bicyclic hydrocarbons, and bicyclo[1.1.1]pentanes (BCPs) in particular, are playing an emerging role as saturated bioisosteres in pharmaceutical, agrochemical and materials chemistry. Taking advantage of strain-release strategies, prior synthetic stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e34e12b451a3c008bd3651795bd4c16f
https://doi.org/10.1038/s41557-021-00786-z
https://doi.org/10.1038/s41557-021-00786-z
Autor:
Maximilian D. Palkowitz, Yusuke Takahira, Julien C. Vantourout, Byron K. Peters, Cian Kingston, Yu Kawamata, Phil S. Baran
Publikováno v:
Acc Chem Res
The appeal and promise of synthetic organic electrochemistry have been appreciated over the past century. In terms of redox chemistry, which is frequently encountered when forging new bonds, it is difficult to conceive of a more economical way to add
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9403dc02eca6c4e3e74202834be9cbe
https://doi.org/10.1021/acs.accounts.9b00539
https://doi.org/10.1021/acs.accounts.9b00539
Autor:
Hugh Nakamura, Byron K. Peters, Phil S. Baran, Yusuke Takahira, Chao Li, Solomon H. Reisberg, Yu Kawamata, Longrui Chen, Tamaki Hoshikawa, Pavel K. Mykhailiuk, Miao Chen, Tomoyuki Shibuguchi
Publikováno v:
Synlett. 30:1178-1182
A simple and robust method for electrochemical alkyl C–H fluorination is presented. Using a simple nitrate additive, a widely available fluorine source (Selectfluor), and carbon-based electrodes, a wide variety of activated and unactivated C–H bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af42f6c0b8065891eed5104c281bafa4
https://doi.org/10.1055/s-0037-1611737
https://doi.org/10.1055/s-0037-1611737
Autor:
Yusuke, Takahira, Miao, Chen, Yu, Kawamata, Pavel, Mykhailiuk, Hugh, Nakamura, Byron K, Peters, Solomon H, Reisberg, Chao, Li, Longrui, Chen, Tamaki, Hoshikawa, Tomoyuki, Shibuguchi, Phil S, Baran
Publikováno v:
Synlett
A simple and robust method for electrochemical alkyl C–H fluorination is presented. Using a simple nitrate additive, a widely available fluorine source (Selectfluor), and carbon-based electrodes, a wide variety of activated and unactivated C–H bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::360112b8c1b4fc90e9ba873128481e85
https://pubmed.ncbi.nlm.nih.gov/33767531
https://pubmed.ncbi.nlm.nih.gov/33767531
Autor:
Lucas Mele, Pierre-Georges Echeverria, Pengfei Hu, Phil S. Baran, Christian A. Malapit, Jinjun Li, Byron K. Peters, Pan Wang, Julien C. Vantourout, Shelley D. Minteer
Publikováno v:
J Am Chem Soc
A user-friendly approach is presented to sidestep the venerable Grignard addition to unactivated ketones to access tertiary alcohols by reversing the polarity of the disconnection. In this work a ketone instead acts as a nucleophile when adding to si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd49147f41fc2dcab10c0822003676b2
https://pubmed.ncbi.nlm.nih.gov/33259715
https://pubmed.ncbi.nlm.nih.gov/33259715
Autor:
Christian A. Malapit, Pan Wang, Byron K. Peters, Julien C. Vantourout, Pierre-Georges Echeverria, Jinjun Li, Shelley D. Minteer, Lucas Mele, Pengfei Hu, Phil S. Baran
A user-friendly approach to sidestep the venerable Grignard addition to unactivated ketones to access tertiary alcohols by reversing the polarity of the disconnection. In this work a ketone instead acts as a nucleophile when adding to simple unactiva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8ebc1248863fc953e2633b41b6abd3f
https://doi.org/10.26434/chemrxiv.13139510.v1
https://doi.org/10.26434/chemrxiv.13139510.v1
