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Organolead-Mediated Arylations: 2-(3,3-Diphenylallyloxy)phenyllead Triacetate as an Internal Free-Radical-Trap-Containing Reagent
2‐(3,3‐Diphenylprop‐2‐enyloxy)phenyllead triacetate, an arylating reagent containing an internal free radical trap, was synthesised and its behaviour studied in base‐catalysed C‐arylation reactions and in copper‐catalysed N‐arylation reactions. The absence of benzofuran derivatives among the product...
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Published in: | European journal of organic chemistry 2004-05, Vol.2004 (9), p.2040-2045 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 2‐(3,3‐Diphenylprop‐2‐enyloxy)phenyllead triacetate, an arylating reagent containing an internal free radical trap, was synthesised and its behaviour studied in base‐catalysed C‐arylation reactions and in copper‐catalysed N‐arylation reactions. The absence of benzofuran derivatives among the products of C‐ and N‐arylation reactions excludes the involvement of radical species in these two processes. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) |
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ISSN: | 1434-193X 1099-0690 |
DOI: | 10.1002/ejoc.200300784 |