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Molecules 2016, 21(11), 1573; doi:10.3390/molecules21111573

Chiral Hypervalent, Pentacoordinated Phosphoranes

1
Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland
2
Department of Chemistry, Environment Protection and Biotechnology, Jan Dlugosz University in Czestochowa, Armii Krajowej Ave. 13/15, 42-200 Czestochowa, Poland
These authors contributed equally to this work.
*
Authors to whom correspondence should be addressed.
Academic Editor: György Keglevich
Received: 29 September 2016 / Revised: 2 November 2016 / Accepted: 16 November 2016 / Published: 21 November 2016
(This article belongs to the Special Issue Recent Advances in Organophosphorus Chemistry)

Abstract

This review presents synthetic procedures applied to the preparation of chiral (mainly optically active) pentacoordinated, hypervalent mono and bicyclic phosphoranes. The mechanisms of their stereoisomerization and their selected interconversions are also presented. View Full-Text
Keywords: hypervalency; chirality; phosphoranes; Berry pseudorotation; turnstile rotation hypervalency; chirality; phosphoranes; Berry pseudorotation; turnstile rotation
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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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MDPI and ACS Style

Krasowska, D.; Chrzanowski, J.; Kiełbasiński, P.; Drabowicz, J. Chiral Hypervalent, Pentacoordinated Phosphoranes. Molecules 2016, 21, 1573.

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