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Ian R. Baxendale
Ian R. Baxendale
Department of Chemistry, University of Durham
Verified email at durham.ac.uk
Title
Cited by
Cited by
Year
Multi-step organic synthesis using solid-supported reagents and scavengers: a new paradigm in chemical library generation
SV Ley, IR Baxendale, RN Bream, PS Jackson, AG Leach, ...
Journal of the Chemical Society, Perkin Transactions 1, 3815-4195, 2000
9582000
An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles
M Baumann, IR Baxendale
Beilstein journal of organic chemistry 9 (1), 2265-2319, 2013
7932013
An overview of the key routes to the best selling 5-membered ring heterocyclic pharmaceuticals
M Baumann, IR Baxendale, SV Ley, N Nikbin
Beilstein Journal of Organic Chemistry 7 (1), 442-495, 2011
5962011
The molecular basis for selective inhibition of unconventional mRNA splicing by an IRE1-binding small molecule
BCS Cross, PJ Bond, PG Sadowski, BK Jha, J Zak, JM Goodman, ...
Proceedings of the National Academy of Sciences 109 (15), E869-E878, 2012
5772012
The synthesis of active pharmaceutical ingredients (APIs) using continuous flow chemistry
M Baumann, IR Baxendale
Beilstein journal of organic chemistry 11 (1), 1194-1219, 2015
3882015
The use of gases in flow synthesis
CJ Mallia, IR Baxendale
Organic Process Research & Development 20 (2), 327-360, 2016
3472016
New tools and concepts for modern organic synthesis
SV Ley, IR Baxendale
Nature Reviews Drug Discovery 1 (8), 573-586, 2002
3472002
Flow ozonolysis using a semipermeable Teflon AF-2400 membrane to effect gas− liquid contact
M O’Brien, IR Baxendale, SV Ley
Organic letters 12 (7), 1596-1598, 2010
3382010
Microwave‐assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous‐flow transformations
IR Baxendale, CM Griffiths‐Jones, SV Ley, GK Tranmer
Chemistry–A European Journal 12 (16), 4407-4416, 2006
3062006
ReactIR flow cell: a new analytical tool for continuous flow chemical processing
CF Carter, H Lange, SV Ley, IR Baxendale, B Wittkamp, JG Goode, ...
Organic Process Research & Development 14 (2), 393-404, 2010
2972010
The integration of flow reactors into synthetic organic chemistry
IR Baxendale
Journal of Chemical Technology & Biotechnology 88 (4), 519-552, 2013
2952013
Multistep synthesis using modular flow reactors: Bestmann–Ohira reagent for the formation of alkynes and triazoles
IR Baxendale, SV Ley, AC Mansfield, CD Smith
Angewandte Chemie 121 (22), 4077-4081, 2009
2632009
The continuous‐flow synthesis of carboxylic acids using CO2 in a tube‐in‐tube gas permeable membrane reactor
A Polyzos, M O'Brien, TP Petersen, IR Baxendale, SV Ley
Angewandte Chemie-International Edition 50 (5), 1190, 2011
2602011
A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly
IR Baxendale, J Deeley, CM Griffiths-Jones, SV Ley, S Saaby, ...
Chemical communications, 2566-2568, 2006
2422006
Hydrogenation in flow: Homogeneous and heterogeneous catalysis using Teflon AF-2400 to effect gas–liquid contact at elevated pressure
M O'Brien, N Taylor, A Polyzos, IR Baxendale, SV Ley
Chemical Science 2 (7), 1250-1257, 2011
2372011
KMnO4-Mediated Oxidation as a Continuous Flow Process
J Sedelmeier, SV Ley, IR Baxendale, M Baumann
Organic letters 12 (16), 3618-3621, 2010
2292010
A flow-based synthesis of Imatinib: the API of Gleevec
MD Hopkin, IR Baxendale, SV Ley
Chemical communications 46 (14), 2450-2452, 2010
2182010
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, ...
Journal of pharmaceutical sciences 104 (3), 781-791, 2015
1962015
Total syntheses of natural products containing spirocarbocycles
LK Smith, IR Baxendale
Organic & Biomolecular Chemistry 13 (39), 9907-9933, 2015
1922015
Total synthesis of the amaryllidaceae alkaloid (+)‐plicamine and its unnatural enantiomer by using solid‐supported reagents and scavengers in a multistep sequence of reactions
IR Baxendale, SV Ley, C Piutti
Angewandte Chemie 114 (12), 2298-2301, 2002
1862002
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Articles 1–20