Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Benjamin A. Chalmers"'
Publikováno v:
European Journal of Organic Chemistry. 2021:6652-6657
Autor:
James J. De Voss, G. Paul Savage, Maree T. Smith, Glen M. Boyle, Benjamin A. Chalmers, John Tsanaktsidis, Jeanette E. Stok, Vicky M. Avery, Paul V. Bernhardt, Hui Xing, Melissa Sykes, Craig M. Williams, Sevan D. Houston, Clementina Farfan Soto, Jed M. Burns, Tyler Fahrenhorst-Jones
Publikováno v:
Organic & Biomolecular Chemistry. 17:6790-6798
The cubane phenyl ring bioisostere paradigm was further explored in an extensive study covering a wide range of pharmaceutical and agrochemical templates, which included antibiotics (cefaclor, penicillin G) and antihistamine (diphenhydramine), a smoo
Publikováno v:
European Polymer Journal. 97:129-137
Sequential Reversible Addition Fragmentation Chain Transfer (RAFT) polymerizations using 2,2′-azobis[2-(2-imidazolin-2-yl)propane]dihydrochloride (VA-044) and 2-(dodecylthiocarbonothioylthio)-2-methylpropionic acid (DDMAT) were used to give amphiph
Publikováno v:
Organicbiomolecular chemistry. 17(5)
The first enantioselective synthesis of (R)-2-cubylglycine, an analogue of (R)-2-phenylglycine in which the phenyl ring has been replaced by cubane, is disclosed. The key step was a telescoped Strecker reaction using (S)-2-amino-2-phenylethanol as a
Autor:
Susan K. Nilsson, Andy Kuo, Hui Xing, Andrea Reitsma, James J. De Voss, Maree T. Smith, David A. Winkler, Paul V. Bernhardt, Cody‐Ellen P. Murray, Carly J. Pierce, Sevan D. Houston, Benjamin A. Chalmers, Helen M. Cooper, Gimme H. Walter, John Tsanaktsidis, Jeanette E. Stok, James S. McCarthy, Sussan Ghassabian, Glen M. Boyle, Benjamin Cao, Charlotte Clark, Peter G. Parsons, Craig M. Williams, Cielo Pasay, Stuart W. Littler, G. Paul Savage
Publikováno v:
Angewandte Chemie International Edition. 55:3580-3585
Pharmaceutical and agrochemical discovery programs are under considerable pressure to meet increasing global demand and thus require constant innovation. Classical hydrocarbon scaffolds have long assisted in bringing new molecules to the market place
Autor:
Cielo Pasay, John Tsanaktsidis, Jeanette E. Stok, Craig M. Williams, Carly J. Pierce, Hui Xing, James S. McCarthy, Benjamin Cao, Sevan D. Houston, Andy Kuo, James J. De Voss, Peter G. Parsons, Charlotte Clark, Glen M. Boyle, Sussan Ghassabian, Paul V. Bernhardt, Susan K. Nilsson, Maree T. Smith, David A. Winkler, Benjamin A. Chalmers, Cody Ellen P. Murray, Helen M. Cooper, Stuart W. Littler, Gimme H. Walter, Andrea Reitsma, G. Paul Savage
Publikováno v:
Angewandte Chemie (International ed. in English). 57(28)
In this Communication, a La Trobe University affiliation is missing for the author David A. Winkler. The penultimate author address entry must read: Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, 3052 (Australia) and La Tr
Autor:
Fawaz Aldabbagh, Benjamin A. Chalmers, Abdullah Alzahrani, Styliana I. Mirallai, Patrick McArdle
The traditional thermal Mannich reaction is unsuitable for preparing polymerizable N-methylene amino substituted acrylamides and methacrylamides. Herein we provide a facile multi-gram high yield synthesis of these monomeric precursors to stimuli-resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d42f28f1318d125719c54049f3cfdff8
http://hdl.handle.net/10379/10235
http://hdl.handle.net/10379/10235
Autor:
Benjamin A. Chalmers
The cubane core has been shown to be physically similar to benzene across the body diagonal, yet remains electronically and physically different in all other ways. It is proposed that this similarity may allow cubane to act as a bioisostere for benze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebacfe605ff24446973c2328a009e8ae
https://doi.org/10.14264/uql.2017.800
https://doi.org/10.14264/uql.2017.800
Publikováno v:
European Journal of Organic Chemistry. 2013:853-857
The robust and diversely useful isoindoline nitroxide, 5-carboxy-1,1,3,3-tetramethylisoindolin-2-yloxyl (1; CTMIO), has previously been synthesised in low-to-moderate yields from phthalic anhydride (3). Recent interest in its biological potential as