Highly stereoselective and catalyst-free synthesis of annulated tetrahydropyridines by intramolecular imino-Diels–Alder reaction under microwave irradiation in water-Reference-Cited by-同舟云学术

Highly stereoselective and catalyst-free synthesis of annulated tetrahydropyridines by intramolecular imino-Diels–Alder reaction under microwave irradiation in water

Published:2016 Issue:13 Volume:18 Page:3712-3717
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Lezana Nicolás¹²³⁴⁵,Matus-Pérez Massiel¹²³⁴⁵,Galdámez Antonio¹²³⁴⁵,Lühr Susan⁶⁷⁸⁹⁵,Vilches-Herrera Marcelo¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. Faculty of Sciences

3. University of Chile

4. 7800024 Nuñoa

5. Chile

6. Department of Materials Science

7. Faculty of Chemistry and Biology

8. University of Santiago of Chile

9. 9170022 Estación Central

Abstract

Highly stereoselective intramolecular imino-Diels–Alder reaction without any catalyst in water and under microwave irradiation for the synthesis of complex organic systems.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/GC/C6GC00912C

Reference33 articles.

1. Catalytic enantioselective [4 + 2]-cycloaddition: a strategy to access aza-hexacycles

2. Understanding the mechanism of the Povarov reaction. A DFT study

3. Intramolecular Hetero-Diels-Alder Reaction of Prolinal-Derived N-Arylimines Lewis Acid-Dependent Reversal of the Diastereoselectivity

4. Lewis Acid Activated Aza-Diels-Alder Reaction ofN-(3-Pyridyl)aldimines: An Experimental and Computational Study

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