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Hydroformylation of Olefinic Derivatives of Isosorbide and Isomannide

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journal contribution
posted on 29.07.2016, 00:00 by Piret Villo, Livia Matt, Lauri Toom, Ilme Liblikas, Tõnis Pehk, Lauri Vares
The first time application of hydroformylation on olefinic derivatives of isosorbide and isomannide is shown by which a new carbon–carbon bond is formed. Depending on the ligand and reaction conditions used, the C6 regioisomer a can be obtained in 4:1 ratio and excellent yield, whereas C5 isomer b is achieved in almost complete regioselectivity (46:1) and good yield. In the majority of cases only the exo orientation is observed for the obtained aldehydes, and the method is easily applicable also on a 1 g scale.

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