Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Briar J. Naysmith"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2325-2342 (2016)
Rising resistance to current clinical antibacterial agents is an imminent threat to global public health and highlights the demand for new lead compounds for drug discovery. One such potential lead compound, the peptide antibiotic teixobactin, was re
Externí odkaz:
https://doaj.org/article/c57ef8f6762f46118891477488a80c57
Autor:
Petrik Galvosas, Ian F. Hermans, Fangrong Zong, David A. J. Herman, Briar J. Naysmith, Kathryn J. Farrand, Ciaran Dolan, David E. Williams, Margaret A. Brimble, Andrew J. McGrath, Richard D. Tilley, Soshan Cheong, Jianyong Jin
Publikováno v:
Journal of Magnetism and Magnetic Materials. 439:251-258
Iron nanoparticles are highly-effective magnetic nanoparticles for T2 magnetic resonance imaging (MRI). However, the stability of their magnetic properties is dependent on good protection of the iron core from oxidation in aqueous media. Here we repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cac14003801761ce9a88e90259858d8e
https://doi.org/10.1016/j.jmmm.2017.04.026
https://doi.org/10.1016/j.jmmm.2017.04.026
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2325-2342 (2016)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Rising resistance to current clinical antibacterial agents is an imminent threat to global public health and highlights the demand for new lead compounds for drug discovery. One such potential lead compound, the peptide antibiotic teixobactin, was re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a4c428c4fec7c33219093dc0e7a2b2b
https://doaj.org/article/c57ef8f6762f46118891477488a80c57
https://doaj.org/article/c57ef8f6762f46118891477488a80c57
Publikováno v:
Tetrahedron. 71:7137-7143
A formal total synthesis of nanaomycin D has been achieved. The strategy employed made use of a one-pot cyclisation–stereoselective reduction of a hydroxyketone to install the pyranonaphthalene moiety after execution of a Hauser–Kraus annulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c19f650eae54a388a21465bf489c5227
https://doi.org/10.1016/j.tet.2014.09.014
https://doi.org/10.1016/j.tet.2014.09.014
Publikováno v:
European Journal of Medicinal Chemistry. 97:816-829
Since the first reported synthesis of an α-carboline almost a century ago, there has been a steady interest in the development of strategies towards this unique heterocyclic motif. This interest can mainly be attributed to a range of biological acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7d322a1744d3930dab9b099d512a229
https://doi.org/10.1016/j.ejmech.2014.11.038
https://doi.org/10.1016/j.ejmech.2014.11.038
Publikováno v:
The Journal of Organic Chemistry. 79:7169-7178
A full account of our efforts toward an asymmetric synthesis of crisamicin A are presented. The key steps include a Hauser-Kraus annulation of a cyanophthalide with a chiral enone-lactone, a stereoselective cyclization-reduction to install the pyran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9c237e56ce7b5b73e21706b5c260faa
https://doi.org/10.1021/jo501344c
https://doi.org/10.1021/jo501344c
Publikováno v:
Tetrahedron. 70:1199-1206
The synthesis of an advanced pyranonaphthalene spiroketal as an intermediate for the total synthesis of griseusin B is described. A one-pot Hauser–Kraus annulation–methylation via reaction of a highly-substituted enone with a cyanophthalide was e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3da7f486debfe9ad330ead6ed3bb633
https://doi.org/10.1016/j.tet.2013.12.066
https://doi.org/10.1016/j.tet.2013.12.066
Publikováno v:
Natural product reports. 34(1)
Covering: 2008 to 2015. A review on the isolation, biological activity and synthesis of pyranonaphthoquinone natural products from 2008–2015 is provided This review discusses the isolation, biological activity and synthesis of pyranonaphthoquinone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af7985c410c2c681d2e163a223e72956
https://pubmed.ncbi.nlm.nih.gov/27759131
https://pubmed.ncbi.nlm.nih.gov/27759131
Publikováno v:
ChemInform. 46
Since the first reported synthesis of an α-carboline almost a century ago, there has been a steady interest in the development of strategies towards this unique heterocyclic motif. This interest can mainly be attributed to a range of biological acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5c8d09b53c5b9ff16c6ab176926b7c2
https://doi.org/10.1002/chin.201532270
https://doi.org/10.1002/chin.201532270
Publikováno v:
ChemInform. 45
The synthesis of an advanced pyranonaphthalene spiroketal as an intermediate for the total synthesis of griseusin B is described. A one-pot Hauser–Kraus annulation–methylation via reaction of a highly-substituted enone with a cyanophthalide was e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d8dc380113c6fc9da5ba3a60d72265c
https://doi.org/10.1002/chin.201429111
https://doi.org/10.1002/chin.201429111