A new synthetic alternative to the synthesis of 3-methyl indoles and 3-methyl indoline-2-ols with an excellent atomic economy is presented in this study. It is demonstrated that the intramolecular interrupted hydroaminomethylation (HAM) reaction is a powerful tool for the formation of these compounds, which exhibit wide-ranging biological activity. Several -Protected-2-vinyl anilines were synthesized and involved in the reaction producing the corresponding 3-methylindole or 3-methyl indoline-2-ol depending on the nature of the -protecting groups.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840357 | PMC |
http://dx.doi.org/10.3390/molecules27031074 | DOI Listing |
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