Mild oxidation of tosylmethylisocyanide to tosylmethylisocyanate: utility in synthetic and medicinal chemistry.

Tetrahedron Lett

Department of Chemistry & Chemical Biology, Baker Laboratory, Cornell University, Ithaca, NY 14853-1301.

Published: March 2014

A convenient and efficient (one-step) oxidation is reported of commercially available tosylmethylisocyanide (TOSMIC) to form tosylmethylisocyanate, making this highly reactive bifunctional molecule a readily available synthetic reagent. Besides engaging in nucleophilic addition reactions with alcohols, amines and thiols, tosylmethylisocyanate also reacts with carboxylic acids to form tosylmethylamides, which undergo substitution reactions in the presence of organocopper and organomagnesium reagents.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001987PMC
http://dx.doi.org/10.1016/j.tetlet.2014.02.016DOI Listing

Publication Analysis

Top Keywords

mild oxidation
4
oxidation tosylmethylisocyanide
4
tosylmethylisocyanide tosylmethylisocyanate
4
tosylmethylisocyanate utility
4
utility synthetic
4
synthetic medicinal
4
medicinal chemistry
4
chemistry convenient
4
convenient efficient
4
efficient one-step
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!