Cp2TiCl2-catalyzed highly regioselective hydroamination of styrenes with hydroxylamines
Author:
Affiliation:
1. MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology
2. Department of Chemistry
3. Tsinghua University
4. Beijing 100084
5. China
Abstract
An efficient Cp2TiCl2-catalyzed one-pot two-step hydroamination procedure that allows the direct formation of tertiary amines from styrenes and an electrophilic nitrogen source has been reported with high regioselectivity.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/QO/C7QO01068K
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