
Shared posts
[ASAP] Nickel-Catalyzed Arylation of C(sp3)–O Bonds in Allylic Alkyl Ethers with Organoboron Compounds
Berthold Hoge
“My favorite saying is ‘diamonds are created under pressure’. … My first experiment was to blow up a tin can using a mixture of sugar and saltpeter . …” Find out more about Berthold Hoge in his Author Profile.
[ASAP] Citrofulvicin, an Antiosteoporotic Polyketide from Penicillium velutinum
Hydrodehalogenation of Haloarenes by a Sodium Hydride–Iodide Composite
Abstract
A simple protocol for hydrodebromination and -deiodination of halo(hetero)arenes was enabled by sodium hydride (NaH) in the presence of lithium iodide (LiI). Mechanistic studies showed that an unusual concerted nucleophilic aromatic substitution operates in the present process.
A simple protocol for hydrodebromination and -deiodination of halo(hetero)arenes was enabled by sodium hydride (NaH) in the presence of lithium iodide (LiI). Mechanistic studies show that an unusual concerted nucleophilic aromatic substitution operates in the present process.
Direct assembly of multiply oxygenated carbon chains by decarbonylative radical–radical coupling reactions

Nature Chemistry. doi:10.1038/nchem.2639
Authors: Kengo Masuda, Masanori Nagatomo & Masayuki Inoue
Pentoses and hexoses represent important structural motifs in bioactive secondary metabolites, though their synthesis often requires several elongation steps. Now, a method for radical–radical coupling reactions of sugar derivatives enables the single-step preparation of the oxygenated carbon chains of several natural products, including sagittamide D, maitotoxin and hikizimycin.

