Synthesis of β-alkoxy-N-protected phenethylamines via one-pot copper-catalyzed aziridination and ring opening-Reference-Cited by-同舟云学术

Synthesis of β-alkoxy-N-protected phenethylamines via one-pot copper-catalyzed aziridination and ring opening

Published:2018 Issue:49 Volume:8 Page:27919-27923
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Saavedra-Olavarría Jorge¹²³⁴⁵,Madrid-Rojas Matías⁶⁷⁸⁴⁵,Almodovar Iriux⁶⁷⁸⁴⁵,Hermosilla-Ibáñez Patricio⁶⁷⁸⁴⁵,Pérez Edwin G.¹²³⁴⁵^ORCID

Affiliation:

1. Department of Organic Chemistry

2. Faculty of Chemistry

3. Pontificia Universidad Católica de Chile

4. Santiago

5. Chile

6. Facultad de Química y Biología

7. Universidad de Santiago de Chile

8. USACh

Abstract

An efficient, regioselective and rapid copper-catalyzed one-pot aminoalkoxylation of styrenes has been developed using different alcohols and phenyl iminoiodinanes.

Funder

Fondo Nacional de Desarrollo Científico y Tecnológico

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA03815E

Reference45 articles.

1. P. A. S.Lowden , in Aziridine Natural Products , ed. A. K. Yudin , Wiley-VCH , Weinheim , 2006 , pp. 399–442

2. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

3. Organocatalytic Asymmetric Epoxidation and Aziridination of Olefins and Their Synthetic Applications

4. Enzymatic Chemistry of Cyclopropane, Epoxide, and Aziridine Biosynthesis

5. Recent advances in the transformations of cycloalkane-fused oxiranes and aziridines

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