Photoredox Catalytic Pentafluorosulfanylative Domino Cyclization of α‐Substituted Alkenes to Oxaheterocycles by Using SF 6-Reference-Cited by-同舟云学术

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Photoredox Catalytic Pentafluorosulfanylative Domino Cyclization of α‐Substituted Alkenes to Oxaheterocycles by Using SF 6

Published:2021-05-11 Issue:31 Volume:27 Page:8088-8093
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Rombach David¹^ORCID,Birenheide Bernhard²,Wagenknecht Hans‐Achim³^ORCID

Affiliation:

1. Laboratory of Inorganic Chemistry Swiss Federal Institute of Technology (ETH) Vladimir-Prelog-Weg 1–5/10 8093 Zürich Switzerland

2. Institute of Inorganic Chemistry Kalsruhe Institute of Technology (KIT) Engesserstr. 15 76131 Karlsruhe Germany

3. Institute of Organic Chemistry Karlsruhe Institute of Technology (KIT) Fritz-Haber-Weg 6 76131 Karlsruhe Germany

Funder

Deutsche Forschungsgemeinschaft

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202100767

Reference63 articles.

1. Trifluoromethylsulfur Pentafluoride

2. Application of the Pentafluorosulfanyl Group as a Bioisosteric Replacement

3. The synthesis and biological activity of pentafluorosulfanyl analogs of fluoxetine, fenfluramine, and norfenfluramine

4. The pentafluorosulfanyl group in cannabinoid receptor ligands: synthesis and comparison with trifluoromethyl and tert-butyl analogues

5. Decomposition of Potent Greenhouse Gas Sulfur Hexafluoride (SF6) by Kirschsteinite-dominant Stainless Steel Slag

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