Zobrazeno 1 - 10
of 171
pro vyhledávání: '"Michael G. Gardiner"'
Autor:
Junyang Xu, Ziwei Hu, Lu Dai, Aditya Yadav, Yashan Jiang, Angelika Bröer, Michael G. Gardiner, Malcolm McLeod, Renhong Yan, Stefan Bröer
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-10 (2024)
Abstract The epithelial neutral amino acid transporter B0AT1 (SLC6A19) is the major transporter for the absorption of neutral amino acids in the intestine and their reabsorption in the kidney. Mouse models have demonstrated that lack of B0AT1 can nor
Externí odkaz:
https://doaj.org/article/f84e5f5f3bc548c8ad53564c9dd50aa8
Autor:
Xin Liu, Paul Carr, Michael G. Gardiner, Martin G. Banwell, Ahmed H. Elbanna, Zeinab G. Khalil, Robert J. Capon
Publikováno v:
ACS Omega, Vol 5, Iss 23, Pp 13926-13939 (2020)
Externí odkaz:
https://doaj.org/article/4834e88797bf4c4abf92ce4f2b22e576
Publikováno v:
ARKIVOC, Vol 2013, Iss 3, Pp 210-226 (2013)
Externí odkaz:
https://doaj.org/article/7840e7f7da954081ad022ff98daa333c
Autor:
Quoc Hoang Pham, Andrew J. Tague, Christopher Richardson, Michael G. Gardiner, Stephen G. Pyne, Christopher J. T. Hyland
Publikováno v:
Chemical Science. 14:4893-4900
Formation of valuable spiroheterocycles with multiple contiguous stereogenic centres from palladium-catalysed enantioselective (3 + 2) cycloaddition reactions of sulfamidate-derived azadienes and vinylcyclopropanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a0e3a774c0a007d755c9742f9df6640
https://doi.org/10.1039/d3sc01510f
https://doi.org/10.1039/d3sc01510f
Autor:
Yi-Min Fan, Madison J. Sowden, Nicholas L. Magann, Erik J. Lindeboom, Michael G. Gardiner, Michael S. Sherburn
Publikováno v:
Journal of the American Chemical Society. 144:20090-20098
The first general synthesis of branched tetraenes ([4]dendralenes) involves two or three steps from inexpensive, commodity chemicals. It involves an unprecedented variation on Suzuki-Miyaura cross-coupling, generating two new C-C bonds in a one-flask
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7f54d0018cafa881ae6d9f18aa35297
https://doi.org/10.1021/jacs.2c09360
https://doi.org/10.1021/jacs.2c09360
Autor:
Liangguang Yi, Yu-Tao He, Shen Tan, Lorenzo V. White, Ping Lan, Michael G. Gardiner, Zhipeng Pei, Michelle L. Coote, Martin G. Banwell
Publikováno v:
The Journal of Organic Chemistry. 87:12287-12296
The readily prepared and vinylated β-carboline
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e7b37f201888833bebaa8fa4c9705d0
https://doi.org/10.1021/acs.joc.2c01477
https://doi.org/10.1021/acs.joc.2c01477
Publikováno v:
ChemistrySelect. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0efe2d0e24f88a7c91bd28ae4b31f955
https://doi.org/10.1002/slct.202300735
https://doi.org/10.1002/slct.202300735
Publikováno v:
Synlett.
A chemoenzymatic approach to the title framework is reported. The reaction sequence starts with the whole-cell biotransformation of iodobenzene and the conversion of the resulting homochiral metabolite into a triene that engages in an intramolecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09c31c07087f1fbb032adb19beef60a7
https://doi.org/10.1055/a-2058-3385
https://doi.org/10.1055/a-2058-3385
Publikováno v:
The Journal of Organic Chemistry. 87:6146-6160
α-Iodo-α,β-unsaturated ketones such as compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d82262e4ce0caca6ba13edaa9cae4ffd
https://doi.org/10.1021/acs.joc.2c00383
https://doi.org/10.1021/acs.joc.2c00383
Publikováno v:
Organic Letters. 24:1268-1273
Acyl bicyclobutanes are shown to engage in strain-promoted cycloaddition reactions with a diverse array of triazolinedione reagents. The synthesis of an orthogonally protected urazole building block enabled the facile preparation of amino acid- and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d02e3a5fdeb8afb8582394336d23bff
https://doi.org/10.1021/acs.orglett.1c04071
https://doi.org/10.1021/acs.orglett.1c04071