700-96-9Relevant articles and documents
Facile introduction of SH group on aromatic substrates via electrophilic substitution reactions
Becht, Jean-Michel,Wagner, Alain,Mioskowski, Charles
, p. 5758 - 5761 (2007/10/03)
Herein, we describe a mild and efficient two-step procedure to introduce a thiol group on aromatic substrates. First, reaction with an activated sulfoxide leads to an arylsulfonium salt intermediate. Then, two successive β-elimination-based dealkylation reactions afford the desired arylthiols in good to excellent yields.
Synthesis and Conformational Analysis of Dibenzodithiocin Derivatives
Sohar, P.,Koevesdi, I.,Szabo, J.,Katocs, A,Fodor, L.,et al.
, p. 760 - 766 (2007/10/02)
N-(3,4-Dialkoxyphenylthiomethyl)aroylamides (1a, b) reacted with phosphoryl chloride to give not only the expected 4H- and 2H-1,3-benzothiazine derivatives (4a, b and 5a, b), but also dibenzodithiocins of new (dibenzodithiocins 2a, b) and known (dibenzodithiocins 3a, b) types.The analogous reaction of the 4-methylaroylamide 8a furnished the 4H-1,3-benzothiazine 9a, the dibenzodithiocin derivative 10a and benzonitrile.In contrast, 8b (the chloro analogue of 8a) furnished only benzonitrile and bis(4-chlorophenylmercapto)methane (11).The structures of the new compounds were confirmed by IR, 1H and 13C NMR, and (in part) by mass spectrometry.Temperature-dependent 1H NMR studies were used for the conformational analysis of 2a and its disulphone 6a; the nature and free enthalpies of activation of the two different conformational motions occuring at higher temperatures were determined.KEY WORDS - Dibenzodithiocins Synthesis 1H and 13C NMR Conformation Structural isomerism
Benzo[b]thiophene derivatives. XXIII. Derivatives of 5,6-dihydroxy-3-benzo[b]thienylacetic acid
Campaigne,Homfeld,Mais
, p. 1351 - 1359 (2007/10/05)
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