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Convenient Route to Super-Expanded Calixpyrroles: Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4)
meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyc...
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Published in: | Organic letters 2000-10, Vol.2 (20), p.3115-3117 |
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container_end_page | 3117 |
container_issue | 20 |
container_start_page | 3115 |
container_title | Organic letters |
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creator | Arumugam, Nagarajan Jang, Yong-Sung Lee, Chang-Hee |
description | meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyclic dodcamer. Effects of catalysts, temperature, inorganic additives, solvent, and reaction concentration were examined. |
doi_str_mv | 10.1021/ol0063196 |
format | article |
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Lett</addtitle><description>meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyclic dodcamer. 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Lett</addtitle><date>2000-10-05</date><risdate>2000</risdate><volume>2</volume><issue>20</issue><spage>3115</spage><epage>3117</epage><pages>3115-3117</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>meso-Alkylporphyrinogen-like cyclic oligomers containing furans and pyrroles have been synthesized by “3 + 2” and “4 + 2” approaches. Condensation of 5,5,10,10,15,15-hexaethyl-21,22-dioxatetrapyrromethane with 2,5-bis[(α-hydroxy-α,α-dimethyl)furan] resulted in the formation of cyclic hexamer and cyclic dodcamer. Effects of catalysts, temperature, inorganic additives, solvent, and reaction concentration were examined.</abstract><pub>American Chemical Society</pub><doi>10.1021/ol0063196</doi><tpages>3</tpages></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Convenient Route to Super-Expanded Calixpyrroles: Synthesis of Calix[n]furano[m]pyrroles (n = 3, 4, 6, 8 and m = 2, 4) |
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