Professor Steven V. Ley Research Group

Publications

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  • Currently displaying 141 - 160 of 1022 publications
Author(s)
Publication title
Journal Name
Publication year
Cyclopropanation using flow-generated diazo compounds.
NM Roda, DN Tran, C Battilocchio, R Labes, RJ Ingham, JM Hawkins, SV Ley
Organic and Biomolecular Chemistry
(2015)
13
(doi: 10.1039/c5ob00019j)
A monolith immobilised iridium Cp* catalyst for hydrogen transfer reactions under flow conditions.
MV Rojo, L Guetzoyan, IR Baxendale
Organic & biomolecular chemistry
(2015)
13
(doi: 10.1039/c4ob02376e)
Transition Metal Catalysis in Aerobic Alcohol Oxidation Foreword
SV Ley
(2015)
28
The rapid synthesis of oxazolines and their heterogeneous oxidation to oxazoles under flow conditions.
S Glöckner, DN Tran, RJ Ingham, S Fenner, ZE Wilson, C Battilocchio, SV Ley
Organic & biomolecular chemistry
(2015)
13
(doi: 10.1039/c4ob02105c)
Foreword
SV Ley
(2015)
2015-January
Achieving Continuous Manufacturing: Technologies and Approaches for Synthesis, Workup, and Isolation of Drug Substance May 20-21, 2014 Continuous Manufacturing Symposium
IR Baxendale, RD Braatz, BK Hodnett, KF Jensen, MD Johnson, P Sharratt, J-P Sherlock, AJ Florence
Journal of pharmaceutical sciences
(2014)
104
(doi: 10.1002/jps.24252)
Total Syntheses of Linear Polythiazole/Oxazole Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B
ZE Wilson, S Fenner, SV Ley
Angew Chem Int Ed Engl
(2014)
54
(doi: 10.1002/anie.201410063)
Sustainable synthesis of thioimidazoles via carbohydrate-based multicomponent reactions
M Baumann, IR Baxendale
Organic Letters
(2014)
16
(doi: 10.1021/ol502845h)
Flow chemistry as a discovery tool to access sp2-sp3 cross-coupling reactions via diazo compounds.
DN Tran, C Battilocchio, S-B Lou, JM Hawkins, SV Ley
Chemical science
(2014)
6
(doi: 10.1039/c4sc03072a)
Facilitating biomimetic syntheses of borrerine derived alkaloids by means of flow-chemical methods
SB Kamptmann, SV Ley
Australian Journal of Chemistry
(2014)
68
(doi: 10.1071/ch14530)
A Systems Approach towards an Intelligent and Self‐Controlling Platform for Integrated Continuous Reaction Sequences
RJ Ingham, C Battilocchio, DE Fitzpatrick, E Sliwinski, JM Hawkins, SV Ley
Angew Chem Int Ed Engl
(2014)
54
(doi: 10.1002/anie.201409356)
Design and Application of a Low-Temperature Continuous Flow Chemistry Platform
JA Newby, DW Blaylock, PM Witt, JC Pastre, MK Zacharova, SV Ley, DL Browne
Organic Process Research and Development
(2014)
18
(doi: 10.1021/op500213j)
Reconfiguration of a Continuous Flow Platform for Extended Operation: Application to a Cryogenic Fluorine-Directed ortho-Lithiation Reaction
JA Newby, DW Blaylock, PM Witt, RM Turner, PL Heider, BH Harji, DL Browne, SV Ley
Organic Process Research and Development
(2014)
18
(doi: 10.1021/op500221s)
A General Continuous Flow Method for Palladium Catalysed Carbonylation Reactions Using Single and Multiple Tube‐in‐Tube Gas‐Liquid Microreactors
U Gross, P Koos, M O'Brien, A Polyzos, SV Ley
European Journal of Organic Chemistry
(2014)
2014
(doi: 10.1002/ejoc.201402804)
Regioselective preparation of saturated spirocyclic and ring-expanded fused pyrazoles
RR Merchant, DM Allwood, DC Blakemore, SV Ley
J Org Chem
(2014)
79
(doi: 10.1021/jo501624t)
Flow chemistry meets advanced functional materials.
RM Myers, DE Fitzpatrick, RM Turner, SV Ley
Chemistry – A European Journal
(2014)
20
(doi: 10.1002/chem.201402801)
Expedient preparation of nazlinine and a small library of indole alkaloids using flow electrochemistry as an enabling technology.
MA Kabeshov, B Musio, PRD Murray, DL Browne, SV Ley
Org Lett
(2014)
16
(doi: 10.1021/ol502201d)
Process intensification for the continuous flow hydrogenation of ethyl nicotinate
T Ouchi, C Battilocchio, JM Hawkins, SV Ley
Organic Process Research and Development
(2014)
18
(doi: 10.1021/op500208j)
Synthesis of riboflavines, quinoxalinones and benzodiazepines through chemoselective flow based hydrogenations.
M Baumann, IR Baxendale, CH Hornung, SV Ley, MV Rojo, KA Roper
Molecules
(2014)
19
(doi: 10.3390/molecules19079736)
Synthesis and Use of a Trifluoromethylated Azomethine Ylide Precursor: Ethyl 1-Benzyl-trans-5- (trifluoromethyl)pyrrolidine-3-carboxylate
DM Allwood, DL Browne, SV Ley
Organic Syntheses
(2014)
91
(doi: 10.15277/orgsyn.091.0162)

Papers of Interest

Yusuf Hamied Department of Chemistry
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