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Regiodivergent Synthesis of Oxadiazocines via Dirhodium-Catalyzed Reactivity of Oxazolidines and α-Imino Carbenes

Published inSynlett, vol. 34, no. 12, p. 1472-1476
Publication date2023-04-12
First online date2023-05-31
Abstract

Using electron-rich or electron-poor N-substituted oxazolidines as substrates, selective formation of either ammonium or oxonium ylides is possible in the presence of α-imino carbenes. As such, treatment of 5-membered oxazolidine precursors with N-sulfonyl-1,2,3-triazoles under dirhodium catalysis (2 mol%) affords the regiodivergent synthesis of either 8-membered 1,3,6- or 1,4,6-oxadiazocines upon the initial N or O reactivity with the carbene.

Citation (ISO format)
VIUDES, Olivier et al. Regiodivergent Synthesis of Oxadiazocines via Dirhodium-Catalyzed Reactivity of Oxazolidines and α-Imino Carbenes. In: Synlett, 2023, vol. 34, n° 12, p. 1472–1476. doi: 10.1055/a-2072-4537
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Journal ISSN0936-5214
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