A Simple and Facile Conjugate Addition of Cyclic and Acyclic 1,3‐Diketones to β‐Nitrostyrenes
Abstract A simple synthesis of 3‐hydroxy‐2‐(2‐nitro‐1‐arylethyl)cyclohex‐2‐en‐1‐ones, 3‐hydroxy‐5,5‐dimethyl‐2‐(2‐nitro‐1‐arylethyl)cyclohex‐2‐en‐1‐ones and 4‐hydroxy‐3‐(2‐nitro‐1‐arylethyl)pent‐3‐en‐2‐ones via conjugate addition of cyclic 1,3‐diketones, 1,3‐cyclohexanedione and 5,5‐dimethyl‐1,3‐cyclohexanedione and acyclic 1,3‐diketone, pentane‐2,4‐dione to β‐Nitrostyrenes were reported. This methodology is pleasing with reliability and scalability with gram scale products that can be synthesized.
Authors
- Payal Malvi (ORCID: https://orcid.org/0000-0003-1668-2950)
- Dharmista Mistry (ORCID: https://orcid.org/0009-0009-4006-4547)
- Nikunjana Benjamin Macwan
Institutions
- Algoma University (CA)
- Central University of Gujarat (IN)
Publication Details
- Journal
- Asian Journal of Organic Chemistry
- Published
- 2024-08-13
- DOI
- https://doi.org/10.1002/ajoc.202400355
- Citations
- 2
- Primary Topic
- Chemical Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.50