| Literature DB >> 35275430 |
Daniel J Nasrallah1, Troy E Zehnder1, Jacob R Ludwig1, Daniel C Steigerwald1, John J Kiernicki1,2, Nathaniel K Szymczak1, Corinna S Schindler1.
Abstract
We describe the development of an efficient method for the olefination of hydrazones and oximes. The key design approach that enables this transformation is tuning of the energy/polarity of C=N π-bonds by employing heteroatom functionalities (NR2 , OR). The resulting hydrazones or oximes facilitate olefination with ruthenium alkylidenes. Through this approach, we show that air-stable, commercially available ruthenium alkylidenes provide access to functionalized alkenes (20 examples) in ring-closing reactions with yields up to 88 %.Entities:
Keywords: Alkylidenes; Hydrazones; Olefination; Oximes; Ruthenium
Year: 2022 PMID: 35275430 PMCID: PMC9117432 DOI: 10.1002/anie.202112101
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 16.823