The reaction of arylmethyl isocyanides and arylmethylamines with xanthate esters: a facile and unexpected synthesis of carbamothioates

An unexpected formation of carbamothioates by a sodium hydride-mediated reaction of arylmethyl isocyanides with xanthate esters in DMF is reported. The products thus obtained were compared with the carbamothioates obtained by the sodium hydride-mediated condensation of the corresponding benzylamines...

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Detalles Bibliográficos
Autores principales: Rajeev, Narasimhamurthy, Swaroop, Toreshettahally R, Alrawashdeh, Ahmad I, Rahman, Shofiur, Alodhayb, Abdullah, Anil, Seegehalli M, Kiran, Kuppalli R, Chandra, Georghiou, Paris E, Rangappa, Kanchugarakoppal S, Sadashiva, Maralinganadoddi P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034244/
https://www.ncbi.nlm.nih.gov/pubmed/32117472
http://dx.doi.org/10.3762/bjoc.16.18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034244/
https://www.ncbi.nlm.nih.gov/pubmed/32117472
http://dx.doi.org/10.3762/bjoc.16.18

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