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Transition-metal-free Intramolecular C-H amination of sulfamate esters and N-alkylsulfamides. | LitMetric

Transition-metal-free Intramolecular C-H amination of sulfamate esters and N-alkylsulfamides.

Chem Commun (Camb)

Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Yamadaoka 2-1, Suita, Osaka 565-0871, Japan.

Published: October 2019

AI Article Synopsis

  • This study presents a new method for intramolecular C-H amination of sulfamate esters without using transition metals, utilizing iodine oxidants like tert-butyl hypoiodite (t-BuOI) and N-iodosuccinimide (NIS).
  • The method with NIS is effective not only for sulfamate esters but also for the oxidative cyclization of N-alkylsulfamides.
  • This research offers a potential alternative for C-H amination reactions in organic synthesis.

Article Abstract

The transition-metal-free intramolecular C-H amination of sulfamate esters using iodine oxidants, tert-butyl hypoiodite (t-BuOI) and N-iodosuccinimide (NIS) is reported. A method using NIS was also successfully applied to the oxidative cyclization of N-alkylsulfamides.

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Source
http://dx.doi.org/10.1039/c9cc06410aDOI Listing

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