Direct synthesis of bicyclic guanidines through unprecedented palladium(ii) catalysed diamination with copper chloride as oxidant
Palladium catalysed intramolecular guanidine transfer to alkenes can be accomplished with copper chloride as the oxidant to give bicyclic guanidines with complete selectivity and in high yields.
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2008-05 (20), p.2334 |
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container_title | Chemical communications (Cambridge, England) |
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creator | Hövelmann, Claas H Streuff, Jan Brelot, Lydia Muñiz, Kilian |
description | Palladium catalysed intramolecular guanidine transfer to alkenes can be accomplished with copper chloride as the oxidant to give bicyclic guanidines with complete selectivity and in high yields. |
doi_str_mv | 10.1039/b719479j |
format | Article |
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ispartof | Chemical communications (Cambridge, England), 2008-05 (20), p.2334 |
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language | eng |
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source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Amination Catalysis Copper - chemistry Crystallography, X-Ray Cyclization Guanidines - chemical synthesis Guanidines - chemistry Oxidants - chemistry Palladium - chemistry |
title | Direct synthesis of bicyclic guanidines through unprecedented palladium(ii) catalysed diamination with copper chloride as oxidant |
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