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Chemical Science|April 6, 2018
Unveiling the role of boroxines in metal-free carbon-carbon homologations using diazo compounds and boronic acidsClaudio Bomio, Mikhail A Kabeshov, Arthur R Lit, et al.
ACS Chemical Biology|May 26, 2009
Cancer, chemistry, and the cell: molecules that interact with the neurotensin receptorsRebecca M Myers, James W Shearman, Matthew O Kitching, et al.
Chemmedchem|November 26, 2008
Natural-product-like spiroketals and fused bicyclic acetals as potential therapeutic agents for B-cell chronic lymphocytic leukaemiaLech-Gustav Milroy, Giovanna Zinzalla, François Loiseau, et al.
Organic & Biomolecular Chemistry|November 6, 2014
The rapid synthesis of oxazolines and their heterogeneous oxidation to oxazoles under flow conditionsSteffen Glöckner, Duc N Tran, Richard J Ingham, et al.
Organic & Biomolecular Chemistry|December 14, 2004
Preparation of enantiopure butane-2,3-diacetals of glycolic acid and alkylation reactions leading to alpha-hydroxyacid and amide derivativesSteven V Ley, Elena Diez, Darren J Dixon, et al.
Organic & Biomolecular Chemistry|December 14, 2004
Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chloridesSteven V Ley, Darren J Dixon, Richard T Guy, et al.
Organic & Biomolecular Chemistry|January 21, 2015
Cyclopropanation using flow-generated diazo compoundsNuria M Roda, Duc N Tran, Claudio Battilocchio, et al.
Organic & Biomolecular Chemistry|May 27, 2016
Synthesis of trifluoromethylated isoxazoles and their elaboration through inter- and intra-molecular C-H arylationJian-Siang Poh, Cristina García-Ruiz, Andrea Zúñiga, et al.
Organic Letters|June 17, 2015
Machines vs Malaria: A Flow-Based Preparation of the Drug Candidate OZ439Shing-Hing Lau, Alicia Galván, Rohan R Merchant, et al.
Angewandte Chemie (International Ed. in English)|October 7, 2016
Visible Light Activation of Boronic Esters Enables Efficient Photoredox C(sp2 )-C(sp3 ) Cross-Couplings in FlowFabio Lima, Mikhail A Kabeshov, Duc N Tran, et al.
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