Christopher Hüßler, Martin C. Dietl, Matthias Scherr, Emma Butigan, Robin Heckershoff, Eric F. Lopes, Justin Kahle, Petra Krämer, Frank - Rominger, Matthias Rudolph, Stephen Hashmi
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引用次数: 0
Abstract
Chalcogen-substituted π-extended indolocarbazoles were synthesized through a nucleophilic cyclization of tethered diynes with sulfur, selenium and tellurium sources, followed by a subsequent Pictet-Spengler reaction. These combined synthetic strategies enabled the facile access to heptacyclic π-extended molecules, offering a broad modularity at various stages of the synthesis route. In total, 26 novel heptacyclic compounds were synthesized. Their photophysical and structural properties were investigated experimentally as well as theoretically.
期刊介绍：
Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.
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