A convenient preparation of bipyridines through ligand coupling reaction with a-sulfurane formed by treatment of methyl 2-pyridyl sulfoxide with grignard reagents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. Ligand coupling through σ-sulfurane — complete retention of configuration of 1-phenylethyl group in the reaction of 1-phenylethyl 2-pyridyl sulfoxide with grignard reagent1
2. The Mechanism of the Alkaline Decomposition of Triarylsulfonium Bromide with Phenyllithium
3. The reaction of p,p'-ditolyl sulfoxide with p-tolyllithium evidence for an aryne intermediate
4. Hypervalent sulfur chemistry. Evidence for tetracoordinate sulfur(IV) and tricoordinate sulfur(II) intermediates in the reaction of p-tolyl sulfoxide with p-tolyllithium
5. Pentacoordinate Sulfur Compounds as Intermediates in Organic Reactions
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1. Recent Progress on the Synthesis of Bipyridine Derivatives;Molecules;2024-01-24
2. Alkyl sulfinates as cross-coupling partners for programmable and stereospecific installation of C(sp3) bioisosteres;Nature Chemistry;2023-03-02
3. Recent Progress in C(sp2)–C(sp2) Bond Formation Using Ligand Coupling on Sulfur(IV);Synthesis;2022-07-28
4. Divergent reactivities of 2-pyridyl sulfonate esters. Exceptionally mild access to alkyl bromides and 2-substituted pyridines;Canadian Journal of Chemistry;2021-07
5. Synthesis of Pyridylsulfonium Salts and Their Application in the Formation of Functionalized Bipyridines;Organic Letters;2020-10-22
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