October 25, 2014 11:24 am
I.R. Baxendale, S.C. Schou, J. Sedelmeier, S.V. Ley, Chem. Eur. J. 2010, 16, 89-94.
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http://onlinelibrary.wiley.com/doi/10.1002/chem.200902906/abstract
Multi-step in flow: The palladium-catalysed acylation of terminal alkynes for the synthesis of yne
ones as well as their further transformation to various heterocycles in a continuous-flow mode is presented. Furthermore, an extension of the simple flow configuration that allows for easy batch splitting and the generation of a heterocyclic library is described (see scheme).
Posted by DR ANTHONY MELVIN CRASTO Ph.D
Categories: organic chemistry
Tags: flow reactors, FLOW SYNTHESIS, J. Sedelmeier, S.C. Schou
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Reblogged this on ORGANIC CHEMISTRY SELECT.
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By DR ANTHONY MELVIN CRASTO Ph.D on October 25, 2014 at 11:36 am
Reblogged this on SynthFlow and commented:
Addition from New Drug Approvals — flow chemistry in action
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By totallymicrowave on October 25, 2014 at 1:43 pm