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.

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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
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article

A Simple and Facile Conjugate Addition of Cyclic and Acyclic 1,3‐Diketones to β‐Nitrostyrenes

Payal Malvi, Dharmista Mistry, Nikunjana Benjamin Macwan
2 citations
Asian Journal of Organic Chemistry
Chemical Reaction Mechanisms
0.50
article

A Simple and Facile Conjugate Addition of Cyclic and Acyclic 1,3‐Diketones to β‐Nitrostyrenes

Payal Malvi, Dharmista Mistry, Nikunjana Benjamin Macwan
article en
2 citations

Abstract

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.

Asian Journal of Organic ChemistryVol. 13(11)
Algoma University (CA), Central University of Gujarat (IN)
Openalex Percentile: Top 40%
Chemical Reaction Mechanisms
0.50
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