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Natural product synthesis on the fly – multistep continuous reaction shows the power of automated flow synthesis
Ritter, S. K.; Chemical & Engineering News, 2006, 84(10), 17
A flow reactor process for the synthesis of peptides utilizing immobilized reagents, scavengers and catch and release protocols
Baxendale, I. R.; Ley, S. V.; Smith, C. D.; Tranmer, G. K.; Chem. Commun., 2006, 4835-4837
A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly
Baxendale, I. R.; Deeley, J.; Griffiths-Jones, C. M.; Ley, S. V.; Saaby, S.; Tranmer, G. K.; Chem. Commun., 2006, 2566-2568
The future of organic synthesis
Kundig, P.; Science, 2006, 314, 430-431
Tools for efficient high-throughput synthesis
Chighine, A.; Sechi, G.; Bradley, M.; Drug Discovery Today, 2007, 12, 459-464
The changing face of organic synthesis
Ley, S. V.; Baxendale, I. R.; Chimia, 2008, 62(3), 162-168
High pressure in organic chemistry on the way to miniaturization
Benito-Lopez, F.; Egberink, E. J. M.; Reinhoudt, D. N.; Verboom, W.; Tetrahedron, 2008, 64(43), 10023-10040
Synthesis of tetrazole analogues of amino acids using Fmoc chemistry: isolation of amino free tetrazoles and their incorporation into peptides
Sureshbabu, V. V.; Venkataramanarao, R.; Naik, S. A.; Chennakirshnareddy, G.; Tetrahedron Letters, 2007, 48(39), 7038-7041
Synthesis of a novel C2/C2′-aryl-substituted pyrrolo[2,1-c][1,4]benzodiazepine dimer prodrug with improved water solubility and reduced DNA reaction rate
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