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Journal ArticleDOI

New One-Pot Synthesis of (E)-β-Aryl Vinyl Halides from Styrenes

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TLDR
A new, efficient protocol for the highly stereoselective one-pot synthesis of (E)-beta-aryl vinyl iodides and (E-beta- Daryl vinyl bromides from styrenes based on sequential ruthenium-catalyzed silylative coupling-N-halosuccinimide-mediated halodesilylation reactions is reported.
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This article is published in Organic Letters.The article was published on 2009-07-02. It has received 51 citations till now. The article focuses on the topics: Aryl & One-pot synthesis.

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Journal ArticleDOI

Use of Bromine and Bromo-Organic Compounds in Organic Synthesis

TL;DR: The use of bromine and different bromo-organic compounds in organic synthesis is outlined and the scope of these reagents for various organic transformations such as bromination, cohalogenation, oxidation, cyclization, ring-opening reactions, substitution, rearrangement, hydrolysis, catalysis, etc is described briefly.
Journal ArticleDOI

General Copper‐Catalyzed Transformations of Functional Groups from Arylboronic Acids in Water

TL;DR: This study should provide a useful strategy for interconversions of the functional groups on aromatic rings in water under air.
Journal ArticleDOI

Direct synthesis of Z -alkenyl halides through catalytic cross-metathesis

TL;DR: It is shown that previously unknown halo-substituted molybdenum alkylidene species are exceptionally reactive and are able to participate in high-yielding olefin metathesis reactions that afford acyclic 1,2-disubstituting Z-alkenyl halides.
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Room Temperature Copper(II)-Catalyzed Oxidative Cyclization of Enamides to 2,5-Disubstituted Oxazoles via Vinylic C–H Functionalization

TL;DR: A copper-II-catalyzed oxidative cyclization of enamides to oxazoles via vinylic C-H bond functionalization at room temperature is described in this paper.

Direct synthesis of Z-alkenyl halides through catalytic cross-metathesis

TL;DR: In this paper, it was shown that Halo-substituted molybdenum alkylidene species are exceptionally reactive and are able to participate in high-yielding olefin metathesis reactions that afford acyclic 1,2-disubstitized Z-alkenyl halides.
References
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Journal ArticleDOI

Hydrozirconation: A New Transition Metal Reagent for Organic Synthesis

TL;DR: In this article, a procedure for functionalizing alkenes, alkynes, and 1,3-dienes via organozirconium(IV) intermediates is described.
Journal ArticleDOI

Catalysis by transition metal complexes of alkene silylation – recent progress and mechanistic implications

TL;DR: In this article, the mechanism of homogeneous catalysis for silylation of alkenes and silylalkynes with late transition metal complexes is discussed. But the authors focus on the synthesis of substituted vinyl-silicon functionalities.
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