Publication

Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides

Jérôme Waser
2005
Journal paper

Abstract

Conversion of unactivated olefins to azides was achieved with high Markovnikov selectivity for a broad range of alkenes by using 6 mol % Co(BF4).6H2O and ligand I, with 3 equiv of tosyl azide as the nitrogen source and simple silanes (e.g., PhSiH3, tetramethyldisiloxane). [on SciFinder (R)]

Official source

https://infoscience.epfl.ch/record/114962?ln=en

About this result

This page is automatically generated and may contain information that is not correct, complete, up-to-date, or relevant to your search query. The same applies to every other page on this website. Please make sure to verify the information with EPFL's official sources.

Graph Chatbot

Chat with Graph Search

Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.

DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.

Cobalt-Catalyzed Hydroazidation of Olefins: Convenient Access to Alkyl Azides

Graph Chatbot

Chat with Graph Search

Multiple Surface Site Three-Dimensional Structure Determination of a Supported Molecular Catalyst

Ring-Opening Reactions of Aminocyclopropanes and Aminocyclobutanes

Diamine Synthesis via the Nitrogen-Directed Azidation of sigma- and pi-C-C Bonds

Ring-Opening Reactions of Aminocyclopropanes and Aminocyclobutanes

Multiple Surface Site Three-Dimensional Structure Determination of a Supported Molecular Catalyst

Diamine Synthesis via the Nitrogen-Directed Azidation of sigma- and pi-C-C Bonds