Nucleophilic Additions of Organolithium Reagents to Heterocyclic Aldimines

The addition of alkyllithium reagents to heterocyclic aldimines is described. This method is a straightforward two-step procedure from the starting aldehyde and amine with one purification. The ability to use unprotected indole carboxaldehydes as substrates is a key feature of this method that make it an attractive way to synthesize the corresponding amine products.

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Publication Details

Journal
Synlett
Published
2025-04-23
DOI
https://doi.org/10.1055/a-2593-6446
Primary Topic
Coordination Chemistry and Organometallics
Type
article
Field-Weighted Citation Impact
0.00

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article

Nucleophilic Additions of Organolithium Reagents to Heterocyclic Aldimines

Ellen Schneider, Timothy J. Barker, J . M . Baek, Walker Hoisington et al.
Synlett
Coordination Chemistry and Organometallics
article

Nucleophilic Additions of Organolithium Reagents to Heterocyclic Aldimines

Ellen Schneider, Timothy J. Barker, J . M . Baek, Walker Hoisington, Evelyn Galgano
article en

Abstract

The addition of alkyllithium reagents to heterocyclic aldimines is described. This method is a straightforward two-step procedure from the starting aldehyde and amine with one purification. The ability to use unprotected indole carboxaldehydes as substrates is a key feature of this method that make it an attractive way to synthesize the corresponding amine products.

SynlettVol. 36(13)
College of Charleston (US)
National Institute of General Medical Sciences, National Center for Research Resources
Openalex Percentile: Top 94%
Coordination Chemistry and Organometallics
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