Menu
 
Research menu
Jump to menu

Publications:  Dr Christopher Jones

Fang L, Trigiante G, Crespo-Otero R, Philpott MP, Jones CR, Watkinson M(2019). An alternative modular 'click-SNAr-click' approach to develop subcellular localised fluorescent probes to image mobile Zn2+ . Organic and Biomolecular Chemistry
10.1039/c9ob01855g
https://qmro.qmul.ac.uk/xmlui/handle/123456789/60986
Fang L, Trigiante G, Crespo-Otero R, Hawes CS, Philpott M, Jones CR, Watkinson M(2019). Endoplasmic reticulum targeting fluorescent probes to image mobile Zn2+. Chemical Science
10.1039/c9sc04300d
https://qmro.qmul.ac.uk/xmlui/handle/123456789/60990
Yang Y, Xu Y, Jones C(2019). A Ring Expansion Route to Benzofused N-Heterocycles via Aryne Insertion into 1,3-Diaza-heterocycles. European Journal of Organic Chemistry
10.1002/ejoc.201900570
https://qmro.qmul.ac.uk/xmlui/handle/123456789/57784
Clement P, Trinchera P, Cervantes-Salguero K, Ye Q, Jones CR, Palma M(2019). One‐step chemical strategy for the formation of carbon nanotube junctions in aqueous solution: The Reaction of DNA‐WrappedCarbon Nanotubes with Diazonium Salts. ChemPlusChem Article cplu.201900151,
10.1002/cplu.201900151
https://qmro.qmul.ac.uk/xmlui/handle/123456789/57723
JONES CR, TRINCHERA P, SUN W, kurdi N, Crespo-Otero R, Palomas D, Javid F, Saeed A(2018). Aryne-Mediated Arylation of Hantzsch Esters: Access to Highly Substituted Aryl-dihydropyridines, Aryl-tetrahydropyridines and Spiro[benzocyclobutene-1,1′-(3′,4′-dihydropyridines)]. SYNTHESIS vol. 50, (23)
10.1055/s-0037-1611065
https://qmro.qmul.ac.uk/xmlui/handle/123456789/49943
JONES CR, IDIRIS F, Majesté C, Craven G(2018). Intramolecular hydride transfer onto arynes: redox-neutral and transition metal-free C(sp3)-H functionalization of amines. Chemical Science
10.1039/C8SC00181B
https://qmro.qmul.ac.uk/xmlui/handle/123456789/33651
JONES CR, Idiris FIM(2017). Recent advances in fluoride-free aryne generation from arene precursors. Organic & Biomolecular Chemistry
10.1039/c7ob01947e
https://qmro.qmul.ac.uk/xmlui/handle/123456789/28553
JONES CR, Trinchera P, Sun W, Smith JE, Palomas D, Crespo-Otero R(2017). Intermolecular Aryne Ene Reaction of Hantzsch Esters: Stable Co-valent Ene Adducts from a 1,4-Dihydropyridine Reaction. Organic Letters
10.1021/acs.orglett.7b02272
https://qmro.qmul.ac.uk/xmlui/handle/123456789/25450
Donohoe TJ, Jones CR, Kornahrens AF, Barbosa LCA, Walport LJ, Tatton MR, O'Hagan M, Rathi AH et al.(2013). Total synthesis of the antitumor antibiotic (±)-streptonigrin: first- and second-generation routes for de novo pyridine formation using ring-closing metathesis. J Org Chem vol. 78, (24) 12338-12350.
10.1021/jo402388f
Donohoe TJ, O'Riordan TJC, Peifer M, Jones CR, Miles TJ(2012). Asymmetric synthesis of the fully elaborated pyrrolidinone core of oxazolomycin A. Organic Letters vol. 14, (21) 5460-5463.
10.1021/ol302541j
Jones CR, Baruah PK, Thompson AL, Scheiner S, Smith MD(2012). Can a C-H•••O interaction be a determinant of conformation?. Journal of the American Chemical Society vol. 134, (29) 12064-12071.
10.1021/ja301318a
Neier R, Journot G, R. Jones C, Blangy V(2012). The Hydrogenation of Heterocyclic Calix[4]arenes, a Transformation Leading to Novel Macrocyclic Ligands. HETEROCYCLES vol. 85, (4) 749-749.
10.3987/rev-11-sr(p)8
Donohoe TJ, Jones CR, Barbosa LCA(2011). Total synthesis of (±)-streptonigrin: De novo construction of a pentasubstituted pyridine using ring-closing metathesis. Journal of the American Chemical Society vol. 133, (41) 16418-16421.
10.1021/ja207835w
Jones CR, Dan Panto G, Morrison AJ, Smith MD(2009). Plagiarizing proteins: enhancing efficiency in asymmetric hydrogenbonding catalysis through positive cooperativity. Angewandte Chemie - International Edition vol. 48, (40) 7391-7394.
10.1002/anie.200903063
Jones CR, Qureshi MKN, Truscott FR, Hsu STD, Morrison AJ, Smith MD(2008). A nonpeptidic reverse turn that promotes parallel sheet structure stabilized by C-H⋯O hydrogen bonds in a cyclopropane γ-peptide. Angewandte Chemie - International Edition vol. 47, (37) 7099-7102.
10.1002/anie.200802648
Return to top