An efficient preparative route to substituted alkyl benzenesulfenates, versatile reagents for site-selective sulfenylative cyclizations
A versatile procedure for the synthesis of alkyl benzenesulfenates possessing varied patterns of nuclear substitution is described.
Harring, Scott R.,Livinghouse, Tom
p. 893 - 902
(2007/10/03)
Mechanism of Nucleophilic Substitution Reactions of o-Nitrobenzenesulfenamides: Evidence for a Substitution Proceeding through a Sulfuranide Intermediate
o-Nitrobenzenesulfenamides (1) undergo acid-catalyzed methanolysis (eq 2) in acetonitrile-methanol, affording methyl o-nitrobenzenesulfenate (2).They also undergo acid-catalyzed reaction with a thiol, giving an alkyl o-nitrophenyl disulfide (eq 3).In MeCN
Kice, John L.,Kutateladze, Andrei G.
p. 3298 - 3303
(2007/10/02)
Studies on sulfenamides. VIII. Anodic oxidation of 2-nitrobenzene-sulfenamides derived from secondary cyclic amines
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Sayo,Yamada,Michida
p. 4530 - 4532
(2007/10/02)
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