Abstract
We report the use of N-2,4-dinitrophenyltetrazoles as latent active esters (LAEs) in the synthesis of amide bonds. Activating the tetrazole generates an HOBt-type active ester without the requirement for exogenous coupling agents. The methodology was widely applicable to a range of substrates, with up to quantitative yields obtained. The versatility and functional group tolerance were exemplified with the one-step synthesis of various pharmaceutical agents and the N-acylation of resin-bound peptides.
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CITATION STYLE
Elwood, J. M. L., Henry, M. C., Lopez-Fernandez, J. D., Mowat, J. M., Boyle, M., Buist, B., … Jamieson, C. (2022). Functionalized Tetrazoles as Latent Active Esters in the Synthesis of Amide Bonds. Organic Letters, 24(51), 9491–9496. https://doi.org/10.1021/acs.orglett.2c03971
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