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This article is cited in 9 scientific papers (total in 9 papers)
Annelation of furan rings to arenes
O. A. Omelchukab, A. S. Tikhomirovab, A. E. Shchekotikhinab a D. Mendeleev University of Chemical Technology of Russia
b G. F. Gause Institute of New Antibiotics, Moscow
Abstract:
Benzo[b]furans have been used in various fields of chemistry and technology due to their unique physical, chemical and biological properties. It is primarily a wide range of biological activities of natural and synthetic benzo[b]furan derivatives and their polyfused analogues (naphthofurans, anthrafurans, etc.) that attracts a significant scientific interest in the context of using these heterocycles as privileged scaffolds in drug design. This survey covers those methods for the annelation of a furan ring to arenes that have been developed mostly during the last decade. We also analyze trends in synthetic methods of benzo[b]furans. Some synthetic schemes are highly efficient in the synthesis of polyfunctionalized furan derivatives. The bibliography includes 110 references.
Received: 18.10.2015
Citation:
O. A. Omelchuk, A. S. Tikhomirov, A. E. Shchekotikhin, “Annelation of furan rings to arenes”, Usp. Khim., 85:8 (2016), 817–835; Russian Chem. Reviews, 85:8 (2016), 817–835
Linking options:
https://www.mathnet.ru/eng/rcr4121https://doi.org/10.1070/RCR4613 https://www.mathnet.ru/eng/rcr/v85/i8/p817
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