Copper-free arylation of 3,3-disubstituted allylic halides with triazene-softened aryl Grignard reagents-Reference-Cited by-同舟云学术

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Copper-free arylation of 3,3-disubstituted allylic halides with triazene-softened aryl Grignard reagents

Published:2015 Issue:22 Volume:13 Page:6333-6337
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Xu Lijun¹²³⁴,Liu Zhubo¹²³⁴,Dong Weipeng¹²³⁴,Song Jinyu¹²³⁴,Miao Maozhong¹²³⁴,Xu Jianfeng¹²³⁴,Ren Hongjun¹²³⁴

Affiliation:

1. Department of Chemistry

2. Zhejiang Sci-Tech University

3. Hangzhou 310018

4. P. R. China

Abstract

A copper-free allylic arylation reaction between 3,3-disubstituted allylic halides and triazene-softened aryl Grignard reagents has been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB00594A

Reference58 articles.

1. Antimicrobial and Antiinsectan Phenolic Metabolites of Dalea searlsiae

2. Monoisoprenylated cyclo-L-alanyl-L-tryptophanyl. Biosynthetic precursor of echinulin

3. Benzyl Derivatives with in Vitro Binding Affinity for Human Opioid and Cannabinoid Receptors from the Fungus Eurotium repens

4. Regioselective Cross-Coupling of Allylboronic Acid Pinacol Ester Derivatives with Aryl Halides via Pd-PEPPSI-IPent

5. Palladium-Catalyzed Completely Linear-Selective Negishi Cross-Coupling of Allylzinc Halides with Aryl and Vinyl Electrophiles

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