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L. Mojovic

Bio: L. Mojovic is an academic researcher from Intelligence and National Security Alliance. The author has contributed to research in topics: Metalation & Pyridazine. The author has an hindex of 3, co-authored 8 publications receiving 92 citations.

Papers
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Journal ArticleDOI
TL;DR: In this article, 3,6-Dichloropyridazine was ortho-lithiated by lithium 2,2,6,6tetramethylpiperidide.

36 citations

Journal ArticleDOI
TL;DR: In this article, conditions for the metalation of 2,6-dichloro and 2, 6-dimethoxy-pyrazine are defined and the lithio-derivatives are shown to react with some electrophiles.

34 citations


Cited by
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Journal ArticleDOI
TL;DR: These TMP(n)MX(m)⋅p LiCl reagents are excellent reagents for converting a wide range of aromatic and heterocyclic substrates into valuable organometallic reagents with broad applications in organic synthesis.
Abstract: The preparation of highly functionalized organometallic compounds can be achieved by direct C-H activation of a broad range of unsaturated substrates using lithium chloride solubilized 2,2,6,6-tetramethylpiperidide bases (TMP(n)MX(m)⋅p LiCl). These are excellent reagents for converting a wide range of aromatic and heterocyclic substrates into valuable organometallic reagents with broad applications in organic synthesis.

331 citations

Journal ArticleDOI
TL;DR: A wide range of polyfunctional aryl and heteroaryl zinc reagents were efficiently prepared in THF via direct zincation using TMPZnCl, a new exceptionally mild and efficient base.

177 citations

Book ChapterDOI
TL;DR: In this article, the directed ortho metalation (DoM) reaction of pyridines, quinolines, pyrimidines and pyrazines has been extensively studied.
Abstract: Publisher Summary This chapter updates the directed ortho metalation (DoM) reaction of pyridines, quinolines, pyrimidines, pyrazines, and pyridazines. Various directed metalation group (DMGs) (halo, NHCOR and NHC02R, OR and OCONR2, 2-oxazolino, CONHR, CONR2, and masked RCHO and RCOR, SO2NR2) have been described, with major emphasis given to the metalation of halo pyridines, an area in which selectivity and mechanistic aspects have been extensively studied. Reactions of powerful alkyllithiums with halo pyridines, quinolines, and diazines may lead to nucleophilic substitution (by addition-elimination or hetaryne mechanisms), ring opening, halogen-scrambling, and coupling reactions that compete with the desired DoM process. Lithiation chemistry of bare pyridines and pyridine N-oxides is presented, followed by the use of the DoM strategy for the synthesis of natural products and biologically active molecules. The exploration of DoM chemistry in haloheteroaromatics is valuable for two reasons: (a) halo derivatives can be readily prepared from accessible amino, hydroxy, and, at times, unsubstituted systems, and (b) halogens can be subsequently induced to undergo a variety of funcionalizations via addition-elimination, metal-halogen exchange, and cross coupling reactions. Some of these transformations are more facile than in the aromatic series. Thus, DoM tactics may lead to diverse substituted heteroaromatics, which can be difficult to obtain by more classical means.

161 citations