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Beilstein J. Org. Chem. 2013, 9, 533–536, doi:10.3762/bjoc.9.58
Graphical Abstract
Figure 1: Classical conversion of tosylate and mesylate into the corresponding nitroalkanes via halides.
Beilstein J. Org. Chem. 2009, 5, No. 23, doi:10.3762/bjoc.5.23
Figure 1: The Uniqsis FlowSyn™ continuous flow reactor comprising of a column holder and heating unit (A) and...
Scheme 1: General procedure for the flow synthesis of α-ketoester products 4a–j.
Scheme 2: General procedure for the batch synthesis of nitroolefinic esters 1a–j.
Scheme 3: General procedure for the flow synthesis of nitroolefinic esters 1a,c.
Figure 2: α-Ketoesters prepared and isolated yields.