Please use this identifier to cite or link to this item:
https://dspace.iiti.ac.in/handle/123456789/9004
| Title: | Microwave-Assisted and Base-Promoted Domino Reaction of Cyclic N-Sulfonyl Ketimines with α,β-Disubstituted Nitroalkenes: A Green Access to 2-Hydroxyarylpyridines |
| Authors: | Guin, Soumitra Majee, Debashis Biswas, Soumen Samanta, Sampak |
| Issue Date: | 2018 |
| Publisher: | Wiley-VCH Verlag |
| Citation: | Guin, S., Majee, D., Biswas, S., & Samanta, S. (2018). Microwave-assisted and base-promoted domino reaction of cyclic N-sulfonyl ketimines with α,β-disubstituted nitroalkenes: A green access to 2-hydroxyarylpyridines. Asian Journal of Organic Chemistry, 7(9), 1810-1814. doi:10.1002/ajoc.201800298 |
| Abstract: | Microwave-assisted and organobase-promoted eco-friendly one-pot protocol has been developed to construct an interesting class of pyridyl-substituted phenols/α-naphthols containing a carboxylate or aroyl group at C2 position on the pyridine ring. A series of N-sulfonyl ketimines and different kinds of bielectrophiles, such as MBH acetates of nitroalkenes/α-arylacetylenyl-β-arylnitroolefins, were involved in this cyclization process, which delivers good to high yields of aforementioned heterocycles and excels with several compatible functionalities. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim |
| URI: | https://doi.org/10.1002/ajoc.201800298 https://dspace.iiti.ac.in/handle/123456789/9004 |
| ISSN: | 2193-5807 |
| Type of Material: | Journal Article |
| Appears in Collections: | Department of Chemistry |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
Altmetric Badge: