Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): efficient formation of products derived from aryl radicals
about
Organic electron donors as powerful single-electron reducing agents in organic synthesis.Hybrid super electron donors - preparation and reactivityFates of imine intermediates in radical cyclizations of N-sulfonylindoles and ene-sulfonamides.Radical cyclizations of cyclic ene sulfonamides occur with β-elimination of sulfonyl radicals to form polycyclic imines.Metal-free reductive cleavage of C-N and S-N bonds by photoactivated electron transfer from a neutral organic donor.Reversible Guest Uptake/Release by Redox-Controlled Assembly/Disassembly of a Coordination Cage.Direct arylation of N-heteroarenes with aryldiazonium salts by photoredox catalysis in water.
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Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): efficient formation of products derived from aryl radicals
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 12 January 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Reduction of arenediazonium salts by tetrakis
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Reduction of arenediazonium sa ...... cts derived from aryl radicals
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type
label
Reduction of arenediazonium salts by tetrakis
@nl
Reduction of arenediazonium sa ...... cts derived from aryl radicals
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prefLabel
Reduction of arenediazonium salts by tetrakis
@nl
Reduction of arenediazonium sa ...... cts derived from aryl radicals
@en
P2860
P356
P1476
Reduction of arenediazonium sa ...... cts derived from aryl radicals
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P2093
Franck LeStrat
Mohan Mahesh
P2860
P356
10.3762/BJOC.5.1
P577
2009-01-12T00:00:00Z