6 research outputs found
Natural products from corals and bacteria: photochemical formation of intricarene and total synthesis of crocagin
Natural products from corals and bacteria: photochemical formation of intricarene and total synthesis of crocagin
Supplementary material for the article: Bihelovic, F.; Stichnoth, D.; Surup, F.; Müller, R.; Trauner, D. Total Synthesis of Crocagin A. Angewandte Chemie - International Edition 2017, 56 (42), 12848–12851. https://doi.org/10.1002/anie.201612641
Supporting information for: [https://doi.org/10.1002/anie.201612641]Related to published version: [http://cherry.chem.bg.ac.rs/handle/123456789/2532
Photochemical formation of intricarene
Sunlight is the ultimate driver of biosynthesis but photochemical steps late in biosynthetic pathways are very rare. They appear to play a role in the formation of certain furanocembranoids isolated from Caribbean corals. One of these compounds, intricarene, has been suspected to arise from an intramolecular 1,3-dipolar cycloaddition involving an oxidopyrylium. Here we show, by a combination of experiments and theory, that the oxidopyrylium forms under photochemical conditions and that its cycloaddition occurs via a triplet state. The formation of a complex by-product can be rationalized by another photochemical step that involves a conical intersection. Our work raises the question whether intricarene is biosynthesized in the natural habitat of the corals or is an artefact formed during workup. It also demonstrates that the determination of exact irradiation spectra, in combination with quantum chemical calculations, enables the rationalization of complex reaction pathways that involve multiple excited states
Supplementary material for the article: Bihelovic, F.; Stichnoth, D.; Surup, F.; Müller, R.; Trauner, D. Total Synthesis of Crocagin A. Angewandte Chemie - International Edition 2017, 56 (42), 12848–12851. https://doi.org/10.1002/anie.201612641
Supporting information for: [https://doi.org/10.1002/anie.201612641]Related to published version: [http://cherry.chem.bg.ac.rs/handle/123456789/2532
The crystal structure of the Dess–Martin periodinane
We report the elusive X-ray structure of the Dess–Martin periodinane (DMP), a hypervalent iodine reagent popular amongst synthetic chemists. In the solid state, the highly crystalline compound forms an intricate coordination polymer held together by intermolecular halogen and hydrogen bonds