[4+2]-Cycloaddition of sterically hindered thiophene S-oxides to alkenes and SO extrusion reactions of the cycloadducts-Reference-Cited by-同舟云学术

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[4+2]-Cycloaddition of sterically hindered thiophene S-oxides to alkenes and SO extrusion reactions of the cycloadducts

Published:2016-04-27 Issue:6 Volume:191 Page:876-884
ISSN:1042-6507
Container-title:Phosphorus, Sulfur, and Silicon and the Related Elements
language:en
Short-container-title:Phosphorus, Sulfur, and Silicon and the Related Elements

Author:

Thiemann Thies¹,Iniesta Jesus²³,Walton David J.⁴

Affiliation:

1. Institute of Materials Chemistry, Kyushu University, Kasuga-koh-en, Kasuga-shi, Japan

2. Institute of Electrochemistry, University of Alicante, San Vicente del Raspeig, Alicante, Spain

3. Physical Chemistry Department, University of Alicante, San Vicente del Raspeig, Alicante, Spain

4. School of Health and Life Sciences, Coventry University, Coventry, United Kingdom

Publisher

Informa UK Limited

Subject

Inorganic Chemistry,Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10426507.2015.1100191

Reference67 articles.

1. An Efficient Route to Benzene and Phenol Derivatives via Ring-Closing Olefin Metathesis

2. An Efficient Route to Benzene and Phenol Derivatives via Ring-Closing Olefin Metathesis

3. Alkynylboronic Esters as Efficient Dienophiles in Cobalt-Catalyzed Diels–Alder Reactions

4. Alkynylboronic Esters as Efficient Dienophiles in Cobalt-Catalyzed Diels–Alder Reactions

5. Nickel-catalyzed [4+2] cycloaddition for highly substituted arenes

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1. An Intramolecular Diels–Alder Approach to the Isoindolinone Core of AZD8154;Organic Process Research & Development;2024-03-13

2. The Oxidation of Oxygen and Sulfur‐Containing Heterocycles by Cytochrome P450 Enzymes;Chemistry – A European Journal;2023-08-02

3. Extrusion Reactions Affording Aromatic Systems, Dienes and Polyenes;Organic Reactions;2022-03-20

4. Thiophenes and Their Benzo Derivatives: Reactivity;Comprehensive Heterocyclic Chemistry IV;2022

5. Trends in the Diels–Alder reaction in polymer chemistry;Chemical Society Reviews;2021

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