A number of 2- and 3-amino-alkanethiols, disulphides, and related substances have been prepared from the corresponding amino-alcohols. The conversion involves esterification with sulphuric acid to aminoalkyl sulphates, cyclisation with carbon disulphide and alkali to thiazolidinethiones, and acid or alkaline hydrolysis of these.
T. C. Owen, J. Chem. Soc. C, 1967, 1373 DOI: 10.1039/J39670001373
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...