Metal- and base-free spirocyclization of alkylidene oxindoles <i>via</i> photo- and mechanochemically-generated nitrile ylides and nitrile imines as 1,3-dipoles

We report an efficient, metal- and base-free synthesis of spiro[pyrrolidine-3,3′-oxindoles] and spiro[indoline-3,3′-pyrazol]-2-ones via 3 + 2 cycloadditions of in situ generated nitrile ylides and nitrile imines with alkylidene oxindoles.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00851d
Citations
1
Primary Topic
Advanced Synthetic Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.94
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article

Metal- and base-free spirocyclization of alkylidene oxindoles via photo- and mechanochemically-generated nitrile ylides and nitrile imines as 1,3-dipoles

Rakesh Ganguly, Subhabrata Sen, Mahesh Kumar Ravva, R. Pandey et al.
1 citations
Organic Chemistry Frontiers
Advanced Synthetic Organic Chemistry
0.94
article

Metal- and base-free spirocyclization of alkylidene oxindoles via photo- and mechanochemically-generated nitrile ylides and nitrile imines as 1,3-dipoles

Rakesh Ganguly, Subhabrata Sen, Mahesh Kumar Ravva, R. Pandey, Shweta Singh, Varun Christopher
article en
1 citations

Abstract

We report an efficient, metal- and base-free synthesis of spiro[pyrrolidine-3,3′-oxindoles] and spiro[indoline-3,3′-pyrazol]-2-ones via 3 + 2 cycloadditions of in situ generated nitrile ylides and nitrile imines with alkylidene oxindoles.

Organic Chemistry FrontiersVol. 12(17)
Shiv Nadar University (IN), SRM University (IN)
Openalex Percentile: Top 24%
Advanced Synthetic Organic Chemistry
0.94
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