Tetrasubstituted Chromanone Synthesis by a Tandem Oxa‐Michael/Michael Addition Reaction of 2‐Hydroxyacetophenones and Alkynyl Nitriles

Abstract An efficient transition metal‐free approach for the synthesis of chroman‐4‐ones via double conjugate addition of 2‐hydroxyacetophenones on alkynyl nitriles utilizing NaH as a base has been realized. This operationally simple protocol offers library of 4‐chromanones in moderate to good yields.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-10-02
DOI
https://doi.org/10.1002/ejoc.202401061
Citations
1
Primary Topic
Synthesis of Organic Compounds
Type
article
Field-Weighted Citation Impact
0.45
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article

Tetrasubstituted Chromanone Synthesis by a Tandem Oxa‐Michael/Michael Addition Reaction of 2‐Hydroxyacetophenones and Alkynyl Nitriles

Avijit Goswami, Madan Kumar, Chandresh Kumari, Narendra Prasad Sahoo
1 citations
European Journal of Organic Chemistry
Synthesis of Organic Compounds
0.45
article

Tetrasubstituted Chromanone Synthesis by a Tandem Oxa‐Michael/Michael Addition Reaction of 2‐Hydroxyacetophenones and Alkynyl Nitriles

Avijit Goswami, Madan Kumar, Chandresh Kumari, Narendra Prasad Sahoo
article en
1 citations

Abstract

Abstract An efficient transition metal‐free approach for the synthesis of chroman‐4‐ones via double conjugate addition of 2‐hydroxyacetophenones on alkynyl nitriles utilizing NaH as a base has been realized. This operationally simple protocol offers library of 4‐chromanones in moderate to good yields.

European Journal of Organic ChemistryVol. 28(3)
Indian Institute of Technology Ropar (IN)
Openalex Percentile: Top 31%
Synthesis of Organic Compounds
0.45
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