Betson M - Search Results

1

Novel C-7 carbon substituted fourth generation fluoroquinolones targeting N. Gonorrhoeae infections.

Kirk R, Betson M, Bingham M, Doyle P, Harvey R, Huxley A, Moat J, Pesnot T, Tait M, Hallworth S, Nelson G. Kirk R, et al. Among authors: betson m. Bioorg Med Chem Lett. 2020 Oct 15;30(20):127428. doi: 10.1016/j.bmcl.2020.127428. Epub 2020 Jul 23. Bioorg Med Chem Lett. 2020. PMID: 32799032

2

Design and synthesis of fluorescent SGLT2 inhibitors.

Lansdell MI, Burring DJ, Hepworth D, Strawbridge M, Graham E, Guyot T, Betson MS, Hart JD. Lansdell MI, et al. Among authors: betson ms. Bioorg Med Chem Lett. 2008 Sep 15;18(18):4944-7. doi: 10.1016/j.bmcl.2008.08.036. Epub 2008 Aug 14. Bioorg Med Chem Lett. 2008. PMID: 18755586

3

A review of methods to synthesise 4'-substituted nucleosides.

Betson M, Allanson N, Wainwright P. Betson M, et al. Org Biomol Chem. 2014 Dec 14;12(46):9291-306. doi: 10.1039/c4ob01449a. Epub 2014 Oct 10. Org Biomol Chem. 2014. PMID: 25302570 Review.

4

Conformational preference in aromatic amides bearing chiral ortho substituents: its origin and application to relayed stereocontrol.

Betson MS, Clayden J, Helliwell M, Johnson P, Lai LW, Pink JH, Stimson CC, Vassiliou N, Westlund N, Yasin SA, Youssef LH. Betson MS, et al. Org Biomol Chem. 2006 Feb 7;4(3):424-43. doi: 10.1039/b514557k. Epub 2005 Dec 22. Org Biomol Chem. 2006. PMID: 16446800

5

The Ireland-Claisen rearrangement as a probe for the diastereoselectivity of nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group.

Betson MS, Fleming I. Betson MS, et al. Org Biomol Chem. 2003 Nov 21;1(22):4005-16. doi: 10.1039/b305881f. Org Biomol Chem. 2003. PMID: 14664389

6

Diastereocontrol in open-chain nucleophilic attack on a double bond adjacent to a stereogenic centre carrying a silyl group.

Betson MS, Fleming I, Ouzman JV. Betson MS, et al. Org Biomol Chem. 2003 Nov 21;1(22):4017-24. doi: 10.1039/b305882d. Org Biomol Chem. 2003. PMID: 14664390

7

Kinetic and thermodynamic stereocontrol in the atroposelective formation of sulfoxides by oxidation of 2-sulfanyl-1-naphthamides.

Betson MS, Clayden J, Helliwell M, Mitjans D. Betson MS, et al. Org Biomol Chem. 2005 Nov 7;3(21):3898-904. doi: 10.1039/b511452g. Epub 2005 Sep 28. Org Biomol Chem. 2005. PMID: 16240006

8

Achieving conformational control over C-C, C-N and C-O bonds in biaryls, N,N'-diarylureas and diaryl ethers: advantages of a relay axis.

Betson MS, Bracegirdle A, Clayden J, Helliwell M, Lund A, Pickworth M, Snape TJ, Worrall CP. Betson MS, et al. Chem Commun (Camb). 2007 Feb 21;(7):754-6. doi: 10.1039/b614618j. Epub 2006 Dec 18. Chem Commun (Camb). 2007. PMID: 17392973

9

Using dipoles to control the directionality of functional groups: syn- and anti-oriented benzene-1,3-dicarboxamides.

Betson MS, Clayden J, Lam HK, Helliwell M. Betson MS, et al. Angew Chem Int Ed Engl. 2005 Feb 11;44(8):1241-4. doi: 10.1002/anie.200461787. Angew Chem Int Ed Engl. 2005. PMID: 15651012 No abstract available.

10

Three groups good, four groups bad? Atropisomerism in ortho-substituted diaryl ethers.

Betson MS, Clayden J, Worrall CP, Peace S. Betson MS, et al. Angew Chem Int Ed Engl. 2006 Sep 4;45(35):5803-7. doi: 10.1002/anie.200601866. Angew Chem Int Ed Engl. 2006. PMID: 16874829 No abstract available.

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