Skip to main navigation Skip to search Skip to main content

Trapping Reactive Intermediates by Mechanochemistry: Elusive Aryl N-Thiocarbamoylbenzotriazoles as Bench-Stable Reagents

  • Vjekoslav Štrukil
  • , Davor Gracin
  • , Oxana V. Magdysyuk
  • , Robert E. Dinnebier
  • , Tomislav Friščic*
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Abstract

Monitoring of mechanochemical thiocarbamoylation by in situ Raman spectroscopy revealed the formation of aryl N-thiocarbamoylbenzotriazoles, reactive intermediates deemed unisolable in solution. The first-time isolation and structural characterization of these elusive molecules demonstrates the ability of mechanochemistry to access otherwise unobtainable intermediates and offers a new range of masked isothiocyanate reagents.

Original languageEnglish
Pages (from-to)8440-8443
Number of pages4
JournalAngewandte Chemie - International Edition
Volume54
Issue number29
DOIs
Publication statusPublished - 13 Jul 2015

Bibliographical note

Publisher Copyright:
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords

  • mechanochemistry
  • reactive intermediates
  • thiocarbamoylation
  • thiourea

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry

Fingerprint

Dive into the research topics of 'Trapping Reactive Intermediates by Mechanochemistry: Elusive Aryl N-Thiocarbamoylbenzotriazoles as Bench-Stable Reagents'. Together they form a unique fingerprint.

Cite this