Electron transfer processes. reactions of 5-nitrofuryl derivatives going by anionradical mechanism
1980 ◽
Vol 45
(12)
◽
pp. 3347-3353
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Keyword(s):
5-Nitrofurfuryl nitrate and bromide (Ia,b) react with electron donors to give 1,2-bis(5-nitro-2-furyl)ethane (II), 1,2-bis(5-nitro-2-furyl)ethylene (III), 5-nitro-2-methylfurane (IV), products of SRN1 reactions Va, Vb and other derivatives. Formation of the derivatives II to V is discussed on the basis of anionradical mechanism. 4-Nitrobenzyl bromide reacts by a SRN1 reaction with 5-nitrofurfuryl phenyl sulphone (Va) in basic medium to give 1-(5-nitro-2-furyl)-1-phenylsulphonyl-2-(4-nitrophenyl)ethane (VIII) and 1-(5-nitro-2-furyl)-2-(4-nitrophenyl)ethylene (IX).
2001 ◽
Vol 5
(2)
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pp. 136-140
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2007 ◽
Vol 11
(05)
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pp. 342-347
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2010 ◽
Vol 11
(2-3)
◽
pp. 73-92
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2018 ◽
Vol 6
(34)
◽
pp. 9065-9070
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2004 ◽
Vol 49
(3)
◽
pp. 445-453
◽
2019 ◽
Vol 16
(2)
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pp. 026018
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