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Petr Sehnal

Researcher at Academy of Sciences of the Czech Republic

Publications -  23
Citations -  1080

Petr Sehnal is an academic researcher from Academy of Sciences of the Czech Republic. The author has contributed to research in topics: Helicene & Enantioselective synthesis. The author has an hindex of 12, co-authored 23 publications receiving 993 citations. Previous affiliations of Petr Sehnal include University of York.

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Emergence of palladium(IV) chemistry in synthesis and catalysis.

TL;DR: The need to comprehensively review catalytic PdIV chemistry, particularly in organic synthesis, was identified, which draws on aspects from both inorganic (organometallic) and organic chemistry fields, and the historical background to organopalladium(IV) chemistry is detailed.
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An organometallic route to long helicenes

TL;DR: An organometallic approach to the derivatives of undecacyclic helicene is reported on, based on intramolecular [2 + 2 + 2] cycloisomerization of aromatic hexaynes under metal catalysis closing 6 new cycles of a helicene backbone in a single operation.
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Asymmetric Synthesis of [7]Helicene-Like Molecules†

TL;DR: A new approach to nonracemic [7]helicene-like molecules has been developed that can be controlled by the absolute configuration at the asymmetric center and by the presence of carbon substituents.
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On the origin of diastereoselectivity in [2 + 2 + 2] cycloisomerization of chiral triynes: controlling helicity of helicene-like compounds by thermodynamic factors.

TL;DR: Diastereoselective CoI-mediated [2 + 2 + 2] cycloisomerization of CH(3)O-substituted optically pure aromatic triynes to obtain nonracemic functionalized helicene-like compounds was studied.
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Helicene‐Based Phosphite Ligands in Asymmetric Transition‐Metal Catalysis: Exploring Rh‐Catalyzed Hydroformylation and Ir‐Catalyzed Allylic Amination

TL;DR: In this article, the first use of helicene-like ligands in asymmetric reactions, including hydroformylation and allylic amination, was presented. And the promising results indicate the potential of the helicene moieties as chiral inductors.