Diels–Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control-Reference-Cited by-同舟云学术

Diels–Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control

Published:2018 Issue:23 Volume:54 Page:2850-2853
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Borisova Kseniya K.¹²³⁴⁵^ORCID,Nikitina Eugeniya V.¹²³⁴⁵^ORCID,Novikov Roman A.⁶⁷⁴⁵^ORCID,Khrustalev Victor N.¹²³⁴⁵^ORCID,Dorovatovskii Pavel V.⁸⁴⁹^ORCID,Zubavichus Yan V.⁸⁴⁹^ORCID,Kuznetsov Maxim L.¹⁰¹¹¹²¹³¹⁴^ORCID,Zaytsev Vladimir P.¹²³⁴⁵^ORCID,Varlamov Alexey V.¹²³⁴⁵^ORCID,Zubkov Fedor I.¹²³⁴⁵^ORCID

Affiliation:

1. Organic Chemistry Department

2. Faculty of Science

3. Peoples’ Friendship University of Russia (RUDN University)

4. Moscow

5. Russian Federation

6. V. A. Engelhardt Institute of Molecular Biology

7. Russian Academy of Sciences

8. National Research Center “Kurchatov Institute”

9. Russia

10. Centro de Química Estrutural

11. Instituto Superior Técnico

12. Universidade de Lisboa

13. Lisbon 1049-001

14. Portugal

Abstract

The tandem [4+2] cycloaddition between hexafluoro-2-butyne and bis-furyl diens can lead to “pincer” or “domino”-adducts.

Funder

Ministry of Education and Science of the Russian Federation

Fundação para a Ciência e a Tecnologia

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C7CC09466C

Reference44 articles.

1. Tandem Intramolecular Diels–Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles: Initial Scope and Applications

2. Intramolecular Diels–Alder reaction as a key step in tandem or sequential processes: a versatile tool for the synthesis of fused and bridged bicyclic or polycyclic compounds

3. The domino way to heterocycles

4. Microwave-assisted tandem Wittig–intramolecular Diels–Alder cycloaddition. Product distribution and stereochemical assignment

5. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions

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