Literature DB >> 26352796

Metal-Free C-Arylation of Nitro Compounds with Diaryliodonium Salts.

Chandan Dey1, Erik Lindstedt1, Berit Olofsson1,2.   

Abstract

An efficient, mild, and metal-free arylation of nitroalkanes with diaryliodonium salts has been developed, giving easy access to tertiary nitro compounds. The reaction proceeds in high yields without the need for excess reagents and can be extended to α-arylation of nitroesters. Nitroalkanes were selectively C-arylated in the presence of other easily arylated functional groups, such as phenols and aliphatic alcohols.

Entities:  

Year:  2015        PMID: 26352796     DOI: 10.1021/acs.orglett.5b02270

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  Highly Diastereoselective Michael Reactions Using β-Nitrocarbonyl Nucleophiles.

Authors:  Amber A S Gietter-Burch; Roxana E Mitrut; Donald A Watson
Journal:  Org Lett       Date:  2015-10-26       Impact factor: 6.005

2.  Competing Pathways in O-Arylations with Diaryliodonium Salts: Mechanistic Insights.

Authors:  Elin Stridfeldt; Erik Lindstedt; Marcus Reitti; Jan Blid; Per-Ola Norrby; Berit Olofsson
Journal:  Chemistry       Date:  2017-09-05       Impact factor: 5.236

3.  Enantioselective Oxidative Rearrangements with Chiral Hypervalent Iodine Reagents.

Authors:  Michael Brown; Ravi Kumar; Julia Rehbein; Thomas Wirth
Journal:  Chemistry       Date:  2016-01-21       Impact factor: 5.236

4.  One-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone-sulfuric acid.

Authors:  Natalia Soldatova; Pavel Postnikov; Olga Kukurina; Viktor V Zhdankin; Akira Yoshimura; Thomas Wirth; Mekhman S Yusubov
Journal:  Beilstein J Org Chem       Date:  2018-04-12       Impact factor: 2.883

  4 in total

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