The Total Synthesis of the Bioactive Natural Product Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B
S Fenner, ZE Wilson, SV Ley
– Chemistry (Weinheim an der Bergstrasse, Germany)
(2016)
22,
15902
(DOI: 10.1002/chem.201603157)
Flow chemistry in Europe
V Hessel, SV Ley
– Journal of Flow Chemistry
(2016)
6,
135
(DOI: 10.1556/1846.2016.22222)
Taming hazardous chemistry by continuous flow technology.
M Movsisyan, EIP Delbeke, JKET Berton, C Battilocchio, SV Ley, CV Stevens
– Chemical Society reviews
(2016)
45,
4892
(DOI: 10.1039/c5cs00902b)
A multicomponent approach for the preparation of homoallylic alcohols.
J-S Poh, S-H Lau, IG Dykes, DN Tran, C Battilocchio, SV Ley
– Chemical Science
(2016)
7,
6803
(DOI: 10.1039/c6sc02581a)
Synthesis of trifluoromethylated isoxazoles and their elaboration through inter- and intra-molecular C–H arylation
J-S Poh, C García-Ruiz, A Zúñiga, F Meroni, DC Blakemore, DL Browne, SV Ley
– Organic & biomolecular chemistry
(2016)
14,
5983
(DOI: 10.1039/c6ob00970k)
Identification and Development of 2,3-Dihydropyrrolo[1,2-<i>a</i>]quinazolin-5(1<i>H</i>)-one Inhibitors Targeting Bromodomains within the Switch/Sucrose Nonfermenting Complex
CL Sutherell, C Tallant, OP Monteiro, C Yapp, JE Fuchs, O Fedorov, P Siejka, S Müller, S Knapp, JD Brenton, PE Brennan, SV Ley
– J Med Chem
(2016)
59,
5095
(DOI: 10.1021/acs.jmedchem.5b01997)
Solvent-Free Continuous Operations Using Small Footprint Reactors: A Key Approach for Process Intensification
T Ouchi, RJ Mutton, V Rojas, DE Fitzpatrick, DG Cork, C Battilocchio, SV Ley
– ACS Sustainable Chemistry and Engineering
(2016)
4,
1912
Solvent-Free Continuous Operations Using Small Footprint Reactors: A Key Approach for Process Intensification
T Ouchi, RJ Mutton, V Rojas, DE Fitzpatrick, DG Cork, C Battilocchio, SV Ley
– ACS Sustainable Chemistry & Engineering
(2016)
4,
1912
Development of the industrial synthesis of vitamin A
GL Parker, LK Smith, IR Baxendale
– Tetrahedron
(2016)
72,
1645
(DOI: 10.1016/j.tet.2016.02.029)
The Generation of a Library of Bromodomain-Containing Protein Modulators Expedited by Continuous Flow Synthesis
P Filipponi, IR Baxendale
– European Journal of Organic Chemistry
(2016)
2016,
2000
(DOI: 10.1002/ejoc.201600222)
Enabling Technologies for the Future of Chemical Synthesis
DE Fitzpatrick, C Battilocchio, SV Ley
– ACS Cent Sci
(2016)
2,
131
(DOI: 10.1021/acscentsci.6b00015)
Iterative reactions of transient boronic acids enable sequential C-C bond formation
C Battilocchio, F Feist, A Hafner, M Simon, DN Tran, DM Allwood, DC Blakemore, SV Ley
– Nature chemistry
(2016)
8,
360
(DOI: 10.1038/NCHEM.2439)
Synthesis of Natural and Unnatural Cyclooligomeric Depsipeptides Enabled by Flow Chemistry.
D Lücke, T Dalton, SV Ley, ZE Wilson
– Chemistry – A European Journal
(2016)
22,
4206
(DOI: 10.1002/chem.201504457)
A multistep continuous flow synthesis machine for the preparation of pyrazoles<i>via</i>a metal-free amine-redox process
J-S Poh, DL Browne, SV Ley
– Reaction Chemistry & Engineering
(2016)
1,
101
(DOI: 10.1039/c5re00082c)
Editorial-Flow Chemistry and Catalysis
SV Ley
– Catalysis Science and Technology
(2016)
6,
4676
(DOI: 10.1039/c6cy90064j)
Controlled generation and use of CO in flow (vol 1, pg 280, 2016)
SVF Hansen, ZE Wilson, T Ulven, SV Ley
– Reaction Chemistry & Engineering
(2016)
1,
340
(DOI: 10.1039/c6re90010k)
Controlled generation and use of CO in flow
SVF Hansen, ZE Wilson, T Ulven, SV Ley
– Reaction Chemistry & Engineering
(2016)
1,
280
(DOI: 10.1039/c6re00020g)
Welcome to <i>Reaction Chemistry & Engineering</i>
SA Khan, IR Baxendale, JM Hawkins, SV Ley, K Jensen, V Hessel, G Luo, D Blackmond, A Katz, DG Vlachos, ME Davis
– Reaction Chemistry & Engineering
(2016)
1,
8
(DOI: 10.1039/c6re90001a)
Online quantitative mass spectrometry for the rapid adaptive optimisation of automated flow reactors
N Holmes, GR Akien, RJD Savage, C Stanetty, IR Baxendale, AJ Blacker, BA Taylor, RL Woodward, RE Meadows, RA Bourne
– Reaction Chemistry and Engineering
(2016)
1,
96
(DOI: 10.1039/c5re00083a)
Continuous photochemistry: the flow synthesis of ibuprofen via a photo-Favorskii rearrangement
M Baumann, IR Baxendale
– Reaction Chemistry and Engineering
(2016)
1,
147
(DOI: 10.1039/c5re00037h)