Abstract

We describe here our results on the addition of 2-amino-benzeneselenol, generated in situ by reaction of bis(2-aminophenyl)-diselenide with H3PO2, to β-dicarbonyl compounds using glycerol as solvent. Depending on the nature of β-dicarbonyl compounds used in reactions, benzoselenazoles or benzoselenazolines were obtained in good yields under mild conditions. When the reactions of in situ generated 2-amino-benzeneselenol were performed with 1,3-diketones, benzoselenazoles were formed in good yields, whereas reactions carried out with β-keto-esters provided benzoselenazolines in high yields.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.