Synthesis of Spirocyclic‐1,2‐Benzisothiazoles by Rh(III)‐Catalyzed [4+1] Annulation of Sulfoximines with Maleimides

Abstract Rh(III)‐catalyzed spiro‐annulation of sulfoximines with maleimides leads to the diastereoselective synthesis of spirocyclic‐1,2‐benzisothiazole heterocycles is disclosed here. This strategy rapidly assembles five‐membered sulfur‐nitrogen‐containing spirocyclic molecules in one‐step. Moreover, the method is scalable and exhibits favourable diastereoselectivity, moderate functional group tolerance, and excellent site‐selectivity.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2024-11-08
DOI
https://doi.org/10.1002/ajoc.202400537
Citations
1
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.25
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article

Synthesis of Spirocyclic‐1,2‐Benzisothiazoles by Rh(III)‐Catalyzed [4+1] Annulation of Sulfoximines with Maleimides

S. N. Reddy, Kandikere Ramaiah Prabhu, Vinayak Hanchate, Anil Kumar
1 citations
Asian Journal of Organic Chemistry
Synthesis and Catalytic Reactions
0.25
article

Synthesis of Spirocyclic‐1,2‐Benzisothiazoles by Rh(III)‐Catalyzed [4+1] Annulation of Sulfoximines with Maleimides

S. N. Reddy, Kandikere Ramaiah Prabhu, Vinayak Hanchate, Anil Kumar
article en
1 citations

Abstract

Abstract Rh(III)‐catalyzed spiro‐annulation of sulfoximines with maleimides leads to the diastereoselective synthesis of spirocyclic‐1,2‐benzisothiazole heterocycles is disclosed here. This strategy rapidly assembles five‐membered sulfur‐nitrogen‐containing spirocyclic molecules in one‐step. Moreover, the method is scalable and exhibits favourable diastereoselectivity, moderate functional group tolerance, and excellent site‐selectivity.

Asian Journal of Organic ChemistryVol. 14(1)
Indian Institute of Science Bangalore (IN)
Openalex Percentile: Top 47%
Synthesis and Catalytic Reactions
0.25
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