Peter Koos
University of Cambridge
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Publication
Featured researches published by Peter Koos.
Organic and Biomolecular Chemistry | 2012
Philippa B. Cranwell; Matthew O'Brien; Duncan L. Browne; Peter Koos; Anastasios Polyzos; Miguel Peña-López; Steven V. Ley
Using a simple and accessible Teflon AF-2400 based tube-in-tube reactor, a series of pyrroles were synthesised in flow using the Paal-Knorr reaction of 1,4-diketones with gaseous ammonia. An inline flow titration technique allowed measurement of the ammonia concentration and its relationship to residence time and temperature.
Chemcatchem | 2013
Samuel L. Bourne; Matthew O'Brien; Sivarajan Kasinathan; Peter Koos; Paeivi Tolstoy; Dennis X. Hu; Roderick W. Bates; Benjamin Martin; Berthold Schenkel; Steven V. Ley
Two tandem flow chemistry processes have been developed. A single palladium‐catalysed Heck reaction with ethylene gas provides an efficient synthesis for functionalised styrenes. Through further elaboration the catalyst becomes multi‐functional and performs a second Heck reaction providing a single continuous process for the synthesis of unsymmetrical stilbenes. In addition, the continuous, rhodium‐catalysed, hydroformylation of styrene derivatives with syngas affords branched aldehydes with good selectivity. Incorporation of an in‐line aqueous wash and liquid–liquid separation allowed for the ethylene Heck reaction to be telescoped into the hydroformylation step such that a single flow synthesis of branched aldehydes directly from aryl iodides was achieved. The tube‐in‐tube semi‐permeable membrane‐based gas reactor and liquid–liquid separator both play an essential role in enabling these telescoped flow processes.
Journal of Organic Chemistry | 2013
Paidi Venkatram Reddy; Julien Smith; Anushree Kamath; Hélène Jamet; Amaël Veyron; Peter Koos; Christian Philouze; Andrew E. Greene; Philippe Delair
Naturally occurring hyacinthacines B1 and B2 have been prepared from a common, easily available, advanced intermediate. The approach features several highly stereoselective transformations: inter alia, a dichloroketene-enol ether [2 + 2] cycloaddition, a Bruylants alkylation, and an amino-nitrile alkylation-reduction.
Organic and Biomolecular Chemistry | 2012
Matthew O'Brien; Peter Koos; Duncan L. Browne; Steven V. Ley
Organic and Biomolecular Chemistry | 2011
Peter Koos; Ulrike Gross; Anastasios Polyzos; Matthew O'Brien; Ian R. Baxendale; Steven V. Ley
Organic Process Research & Development | 2012
Tobias Brodmann; Peter Koos; Albrecht Metzger; Paul Knochel; Steven V. Ley
European Journal of Organic Chemistry | 2014
Ulrike Gross; Peter Koos; Matthew O'Brien; Anastasios Polyzos; Steven V. Ley
Synlett | 2012
Duncan L. Browne; Matthew O'Brien; Peter Koos; Philippa B. Cranwell; Anastasios Polyzos; Steven V. Ley
Synlett | 2011
Samuel L. Bourne; Peter Koos; Matthew O’Brien; Benjamin Martin; Berthold Schenkel; Ian R. Baxendale; Steven V. Ley
Tetrahedron Letters | 2012
Dennis X. Hu; Max Bielitza; Peter Koos; Steven V. Ley
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Commonwealth Scientific and Industrial Research Organisation
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