Rhodium-catalyzed C–H Annulation of Aldonitrones with Allyl Methyl Carbonate

Abstract The Rh(III)-catalyzed, nitrone-directed C–H activation/allylation/1,3-dipolar cycloaddition sequence with C-aryl-N-tert-butyl nitrones and allyl methyl carbonate gives polycyclic isoxazolidines, in many cases with high or complete regioselectivity for products with a condensed ring system (containing a 1-amino-2-hydroxymethyl-indane skeleton).

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Publication Details

Journal
Synlett
Published
2025-11-20
DOI
https://doi.org/10.1055/a-2752-7699
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Rhodium-catalyzed C–H Annulation of Aldonitrones with Allyl Methyl Carbonate

Sylwia Ostrowska, Rafał Loska, Barbara Stańska
1 citations
Synlett
Catalytic C–H Functionalization Methods
0.94
article

Rhodium-catalyzed C–H Annulation of Aldonitrones with Allyl Methyl Carbonate

Sylwia Ostrowska, Rafał Loska, Barbara Stańska
article en
1 citations

Abstract

Abstract The Rh(III)-catalyzed, nitrone-directed C–H activation/allylation/1,3-dipolar cycloaddition sequence with C-aryl-N-tert-butyl nitrones and allyl methyl carbonate gives polycyclic isoxazolidines, in many cases with high or complete regioselectivity for products with a condensed ring system (containing a 1-amino-2-hydroxymethyl-indane skeleton).

SynlettVol. 37(05)
Institute of Organic Chemistry (PL), Adam Mickiewicz University in Poznań (PL), Polish Academy of Sciences (PL)
Openalex Percentile: Top 20%
Catalytic C–H Functionalization Methods
0.94
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