A Mild and Efficient Method for Selective Acetylation of Amines
Shyh‐Chyun Yang, Huey‐Min Wang, Ling‐Ching Chen
Abstract
Shyh‐Chyun Yang, Huey‐Min Wang, Ling‐Ching Chen
Abstract
Abstract Primary and secondary amines were acetylated under mild conditions by means of 3‐acetyl‐1,3‐thiazolidine‐2‐thione [ATT(1)]. The reaction was successfully applied to selective acetylation of a primary amino group of diamines containing a primary and a secondary amino groups or exclusive N‐acetylation of amino alcohols.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract Primary and secondary amines were acetylated under mild conditions by means of 3‐acetyl‐1,3‐thiazolidine‐2‐thione [ATT(1)]. The reaction was successfully applied to selective acetylation of a primary amino group of diamines containing a primary and a secondary amino groups or exclusive N‐acetylation of amino alcohols.
Key concepts: Chemistry, Acetylation, Primary (astronomy), Organic chemistry, Biochemistry, Astronomy, Physics, Gene