A highly regio- and stereoselective method was developed for the preparation of -alkenylpyrazoles and chromenopyrazoles by the reaction of -tosylhydrazones and salicyl -tosylhydrazones with alkynes under neat conditions in the presence of La(OTf). The present study was found to be efficient and convenient for direct access to -alkenylpyrazoles and chromenopyrazoles through C-C, C-N, and C-O bond forming reactions. Structure assignment of -alkenylpyrazole compound was confirmed by X-ray analysis.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.joc.0c02421 | DOI Listing |
J Org Chem
February 2021
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
A highly regio- and stereoselective method was developed for the preparation of -alkenylpyrazoles and chromenopyrazoles by the reaction of -tosylhydrazones and salicyl -tosylhydrazones with alkynes under neat conditions in the presence of La(OTf). The present study was found to be efficient and convenient for direct access to -alkenylpyrazoles and chromenopyrazoles through C-C, C-N, and C-O bond forming reactions. Structure assignment of -alkenylpyrazole compound was confirmed by X-ray analysis.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!