1-Alkyl-(or aryl-) amino-2-methylpropane-2-thiols. Bi-and tetradentate nitrogen-sulfur ligands from Schiff's base disulfides
JL Corbin, DE Work
Index: Corbin,J.L.; Work,D.E. Journal of Organic Chemistry, 1976 , vol. 41, p. 489 - 491
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Citation Number: 38
Abstract
Repetition of a published procedure for the preparation of several N-substituted l-amino-2- methylpropane-2-thiols (2a-d) for use as bidentate ligands indicated that the products characterized therein were not thiols, but the corresponding disulfides (3a-d). Preparation of the authentic thiols was accomplished by reduction of the intermediate Schiff's bases (la-d) with LiAlH4 in refluxing tetrahydrofuran. The novel tetradentate 5 was also synthesized ...
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[D'Amico,J.J.; Dahl,W.E. Journal of Organic Chemistry, 1975 , vol. 40, p. 1224 - 1227]