Issue 6, 2023

AgSbF6-catalyzed C3 aza-Friedel–Crafts alkylation of N,O-acetals with indoles for the synthesis of N-α indole substituted pyrrolidine and piperidine derivatives

Abstract

An efficient approach to access chiral N-α indole substituted pyrrolidine and piperidine skeletons has been developed through a AgSbF6-catalyzed N-α aza-Friedel–Crafts alkylation of N,O-acetals 6a, 6b, 9, and 11a–11d with indoles. As a result, a series of 2,3-trans N-α indole substituted pyrrolidines 8a–8x and piperidines 10a–10j were prepared in moderate to excellent yields and with excellent diastereoselectivities (dr up to 99 : 1). Moreover, several 2,5-cis-N-α indole substituted pyrrolidine derivatives 12a–12k were synthesized according to this strategy with moderate to good yields and diastereoselectivities (dr up to 99 : 1).

Graphical abstract: AgSbF6-catalyzed C3 aza-Friedel–Crafts alkylation of N,O-acetals with indoles for the synthesis of N-α indole substituted pyrrolidine and piperidine derivatives

Supplementary files

Article information

Article type
Paper
Submitted
04 Dec 2022
Accepted
06 Jan 2023
First published
06 Jan 2023

Org. Biomol. Chem., 2023,21, 1303-1315

AgSbF6-catalyzed C3 aza-Friedel–Crafts alkylation of N,O-acetals with indoles for the synthesis of N-α indole substituted pyrrolidine and piperidine derivatives

Y. Zhang, Z. Yi, A. Yang, J. Guo, X. Li and B. Wei, Org. Biomol. Chem., 2023, 21, 1303 DOI: 10.1039/D2OB02213C

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