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Tandem and One-Pot Hydroformylation/Michael Reactions of Acrylates

Fleischer, Ivana and Quintero-Duque, Samuel (2017) Tandem and One-Pot Hydroformylation/Michael Reactions of Acrylates. Synthesis 49 (04), pp. 925-932.

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Other URL: http://doi.org/10.1055/s-0036-1588394


Abstract

The combination of various reactions in one operational step leads to many advantages in synthetic strategies, such as a lower consumption of resources, effort, arid time, when intermittent workup and purification steps can be avoided. The hydroformylation reaction of acrylates gives access to 2-formylpropanoates, which thanks to their structural features constitute useful intermediates in the ...

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Item type:Article
Date:2017
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Arbeitskreis Dr. Ivana Fleischer
Identification Number:
ValueType
10.1055/s-0036-1588394DOI
Keywords:RHODIUM-CATALYZED HYDROFORMYLATION; STEREOSELECTIVE HYDROFORMYLATION; ASYMMETRIC HYDROFORMYLATION; SELECTIVE HYDROFORMYLATION; UNSATURATED ESTERS; METHYL ACRYLATE; COMPLEXES; ALKENES; LIGANDS; OLEFINS; hydroformylation; acrylates; rhodium; one port; tandem; Michael addition
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Item ID:38771
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