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Literature DB >> 16288550

Selective 4-arylation of pyridines by a nonmetalloorganic process.

Abstract

[reaction: see text] Mild and position-selective nucleophilic 4-arylation of pyridines has been accomplished by the use of triflic anhydride N-activation.

Entities: Chemical

Year: 2005 PMID： 16288550 DOI： 10.1021/ol052476z

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

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Cited

6 in total

1. Total synthesis of (+/-)- and (-)-actinophyllic acid.

Authors: Connor L Martin; Larry E Overman; Jason M Rohde
Journal: J Am Chem Soc Date: 2010-04-07 Impact factor: 15.419

2. Azine Activation via Silylium Catalysis.

Authors: Carla Obradors; Benjamin List
Journal: J Am Chem Soc Date: 2021-04-28 Impact factor: 15.419

3. C-H Cyanation of 6-Ring N-Containing Heteroaromatics.

Authors: Bryony L Elbert; Alistair J M Farley; Timothy W Gorman; Tarn C Johnson; Christophe Genicot; Bénédicte Lallemand; Patrick Pasau; Jakub Flasz; José L Castro; Malcolm MacCoss; Robert S Paton; Christopher J Schofield; Martin D Smith; Michael C Willis; Darren J Dixon
Journal: Chemistry Date: 2017-09-22 Impact factor: 5.236

Selective 4-arylation of pyridines by a nonmetalloorganic process.

1. Total synthesis of (+/-)- and (-)-actinophyllic acid.

2. Azine Activation via Silylium Catalysis.

3. C-H Cyanation of 6-Ring N-Containing Heteroaromatics.

4. Practical synthesis of 3-aryl anthranils via an electrophilic aromatic substitution strategy.

5. Practical and Regioselective Synthesis of C-4-Alkylated Pyridines.

6. Synthesis of eunicellane-type bicycles embedding a 1,3-cyclohexadiene moiety.