Michael John Hall

Newcastle University, Newcastle upon Tyne, England, United Kingdom 
"Michael Hall"
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Harry Anderson grad student 1999-1999 Oxford
Jeremy Robertson grad student 1999-2003 Oxford
Donal O'Shea post-doc 2003-2005 University College Dublin (Ireland)
Janine Cossy post-doc 2006-2006 ESPCI ParisTech
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Tyler AR, Ragbirsingh R, McMonagle CJ, et al. (2020) Encapsulated Nanodroplet Crystallization of Organic-Soluble Small Molecules. Chem. 6: 1755-1765
Dzeha T, Nyiro C, Kardasopoulos D, et al. (2018) UV Resistance of bacteria from the Kenyan Marine cyanobacterium Moorea producens. Microbiologyopen. e00697
Baslé A, Hewitt L, Koh A, et al. (2017) Crystal structure of NucB, a biofilm-degrading endonuclease. Nucleic Acids Research
Cowell J, Buck M, Essa AH, et al. (2017) Traceless-Cleavage of Protein-Biotin Conjugates Under Biologically-Compatible Conditions. Chembiochem : a European Journal of Chemical Biology
Tyler AR, Mosaei H, Morton S, et al. (2017) Structural Reassignment and Absolute Stereochemistry of Madurastatin C1 (MBJ-0034) and the Related Aziridine Siderophores: Madurastatins A1, B1, and MBJ-0035. Journal of Natural Products
Baksh A, Kepplinger B, Isah HA, et al. (2016) Production of 17-O-demethyl-geldanamycin, a cytotoxic ansamycin polyketide, by Streptomyces hygroscopicus DEM20745. Natural Product Research. 1-6
Abualnaja M, Waddell PG, Clegg W, et al. (2016) Synthesis of pentacyclic pyrrolo[3,4-a]carbazole-1,3(2H)-diones via an intermolecular Diels–Alder, intramolecular carbonyl-ene reaction strategy Tetrahedron. 72: 5798-5806
Alnoman RB, Rihn S, O'Connor DC, et al. (2015) Circularly Polarized Luminescence from Helically Chiral N,N,O,O-Boron Chelated Dipyrromethenes. Chemistry (Weinheim An Der Bergstrasse, Germany)
Essa AH, Lerrick RI, Çiftçi E, et al. (2015) Grignard-mediated reduction of 2,2,2-trichloro-1-arylethanones. Organic & Biomolecular Chemistry. 13: 5793-803
Cowell J, Abualnaja M, Morton S, et al. (2015) Diastereoselective synthesis of functionalised carbazoles via a sequential Diels-Alder/ene reaction strategy Rsc Advances. 5: 16125-16152
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