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Reynolds et al., 1961 - Google Patents

Mercaptoethylation. III. Reactions of 2-Mercaptoethyl Carbamates

Reynolds et al., 1961

Document ID
8764713648004815497
Author
Reynolds D
Fields D
Johnson D
Publication year
Publication venue
The Journal of Organic Chemistry

External Links

Snippet

Three representative examples of 2-mercaptoethyl carbamates and four different types of S- substituted 2-mercaptoethyl carbamates are shown to be mercaptoethyfating agents for moderately to strongly basic primary and secondary amines. Side reactions encountered in …
Continue reading at pubs.acs.org (other versions)

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    • C07C323/24—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
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