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<field name="value">A straightforward and efficient synthesis of the two less explored types of indolocarbazoles has been&#xd;
developed. Two different processes for the carbazole nucleus preparation, a gold-catalysed regioselective&#xd;
cyclization followed by the dioxomolybdenum-catalysed version of Cadogan reductive cyclization,&#xd;
enables the sequential construction of two carbazole cores. The procedure features total regioselectivity&#xd;
and high overall yields. The required starting α-indol-3-ylalkyl propargylic alcohols are easily and efficiently&#xd;
accessed from commercially available reagents. In addition, the photoluminescent properties of two&#xd;
indolo[2,3-c]carbazoles, with fluorescence quantum yields around 0.7, have been studied.</field>
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<field name="value">Organic Chemistry Frontiers. 2020, v. 7, n. 14, p. 1869-1877</field>
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