Multicomponent synthesis of α-branched amines using organozinc reagents generated from alkyl bromides

• Baptiste Leroux,
• Alexis Beaufils,
• Federico Banchini,
• Olivier Jackowski,
• Alejandro Perez-Luna,
• Fabrice Chemla,
• Marc Presset and
• Erwan Le Gall

Beilstein J. Org. Chem. 2024, 20, 2834–2839, doi:10.3762/bjoc.20.239

• nucleophilic organozincate complexes (e.g., LiBuZnBrCl), which is a well-established process in THF [29][30]. Due to the hygroscopic character of LiCl and the necessity to determine the amount of organozinc by iodolysis [20] in order to adjust the stoichiometry of the reagents for the multicomponent coupling

Deproto-metallation of N-arylated pyrroles and indoles using a mixed lithium–zinc base and regioselectivity-computed CH acidity relationship

• Mohamed Yacine Ameur Messaoud,
• Ghenia Bentabed-Ababsa,
• Madani Hedidi,
• Aïcha Derdour,
• Floris Chevallier,
• Yury S. Halauko,
• Oleg A. Ivashkevich,
• Vadim E. Matulis,
• Laurent Picot,
• Valérie Thiéry,
• Thierry Roisnel,
• Vincent Dorcet and
• Florence Mongin

Beilstein J. Org. Chem. 2015, 11, 1475–1485, doi:10.3762/bjoc.11.160

• deprotonative metallation using the base in situ prepared from LiTMP and ZnCl2·TMEDA (1/3 equiv). With N-phenylpyrrole and -indole, the reactions were carried out in hexane containing TMEDA which regioselectively afforded the 2-iodo derivatives after subsequent iodolysis. With pyrroles and indoles bearing N

• using the DFT B3LYP method in order to rationalize the experimental results. Keywords: CH acidity; indoles; iodolysis; mixed lithium–zinc bases; pyrroles; Introduction Pyrrole occurs in very important natural products such as tetrapyrrolic (linear) bilirubinoids, and (cyclic) porphyrins and corrins

• N-phenylpyrrole (1c). The result has been evidenced by subsequent iodolysis (Scheme 2). Nevertheless, for numerous substrates, THF is an alternative solvent that allows the reactions to be finished after 2 h contact at room temperature [33][34][36]. Among the different methods of trapping that can

Radical zinc-atom-transfer-based carbozincation of haloalkynes with dialkylzincs

• Fabrice Chemla,
• Florian Dulong,
• Franck Ferreira and
• Alejandro Pérez-Luna

Beilstein J. Org. Chem. 2013, 9, 236–245, doi:10.3762/bjoc.9.28

• warming, the zinc carbenoid is stereochemically labile and isomerizes to its more stable form. In the absence of added air, no decomposition of the carbenoid intermediate is observed at room temperature for at least 24 h. Deuterium labeling and iodolysis experiments evidence that the zinc carbenoids

Stereoselective synthesis of tetrasubstituted alkenes via a sequential carbocupration and a new sulfur–lithium exchange

• Andreas Unsinn,
• Cora Dunst and
• Paul Knochel

Beilstein J. Org. Chem. 2012, 8, 2202–2206, doi:10.3762/bjoc.8.248

• iodolysis leading to the iodide 10 in 93% yield. Treatment of 1,2-dibromobenzene with iPrMgCl·LiCl at −15 °C for 2 h followed by a transmetalation with ZnCl2 gives the required zinc reagent 11, which undergoes a Negishi cross-coupling with the iodide 10 at 50 °C (5 h) leading to the alkynyl thioether 1a in