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Published in 2022 at "Organic Letters"
DOI: 10.1021/acs.orglett.2c02983
Abstract: The dearomative (4 + 3) cycloaddition reactions of 3-alkenylindoles with in situ-generated oxyallyl cations furnish cyclohepta[b]indoles, functionality-rich frameworks found in many bioactive compounds, including all pentacyclic ambiguine alkaloids. The analogous reactions between oxyallyl cations and…
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Keywords:
reactions alkenylindoles;
alkenylpyrroles afford;
dearomative cycloaddition;
cyclohepta indoles ... See more keywords