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Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes
In the course of an ongoing synthetic project on cyclic diferrocenylphosphines, we obtained a group of planar–chiral diferrocenyl compounds useful as precursors for subsequent cyclization. Here we report the crystal structures of two symmetric compounds [(Fc(A))(2)(Ph)P], one of which contains fo...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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International Union of Crystallography
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941264/ https://www.ncbi.nlm.nih.gov/pubmed/33664166 http://dx.doi.org/10.1107/S2053229621001996 |
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author | Honegger, Philipp Roller, Alexander Widhalm, Michael |
author_facet | Honegger, Philipp Roller, Alexander Widhalm, Michael |
author_sort | Honegger, Philipp |
collection | PubMed |
description | In the course of an ongoing synthetic project on cyclic diferrocenylphosphines, we obtained a group of planar–chiral diferrocenyl compounds useful as precursors for subsequent cyclization. Here we report the crystal structures of two symmetric compounds [(Fc(A))(2)(Ph)P], one of which contains four stereogenic centres (two C chiral and two planar chiral centres), i.e. 1,1′-(phenylphosphanediyl)bis{(2S (p))-2-[(1R)-1-(acetyloxy)ethyl]ferrocene}, [Fe(2)(C(5)H(5))(2)(C(24)H(25)O(4)P)], and the other phosphine sulfide is a purely planar–chiral compound (two planar chiral centres), i.e. bis[(2S (p))--2-ethenylferrocen-1-yl]phenylphosphane sulfide, [Fe(2)(C(5)H(5))(2)(C(20)H(17)PS)]. Owing to the stereocentres present, reactions performed on [(Fc(A))(2)(Ph)P]-type compounds strongly favour one ferrocene unit over the other due to diastereoselectivity. Furthermore, we present four related structures where the ferrocene units are not identical [(Fc(A))(Fc(B))(Ph)P]. These are {(2S (p))-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}[(2S (p))-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(22)H(21)O(2)PS)], [(2S (p))-2-ethenylferrocen-1-yl]{(2S (p))-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(S)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(20)H(19)OPS)], {(2S (p))-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}{(2S (p))-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(R)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(22)H(23)O(3)PS)], and {(2S (p))-2-[(1R)-1-benzylamino)ethyl]ferrocen-1-yl}[(2S (p))-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(27)H(26)NPS)]. All of the structures are accessible in one step from known precursors. |
format | Online Article Text |
id | pubmed-7941264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-79412642021-03-24 Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes Honegger, Philipp Roller, Alexander Widhalm, Michael Acta Crystallogr C Struct Chem Research Papers In the course of an ongoing synthetic project on cyclic diferrocenylphosphines, we obtained a group of planar–chiral diferrocenyl compounds useful as precursors for subsequent cyclization. Here we report the crystal structures of two symmetric compounds [(Fc(A))(2)(Ph)P], one of which contains four stereogenic centres (two C chiral and two planar chiral centres), i.e. 1,1′-(phenylphosphanediyl)bis{(2S (p))-2-[(1R)-1-(acetyloxy)ethyl]ferrocene}, [Fe(2)(C(5)H(5))(2)(C(24)H(25)O(4)P)], and the other phosphine sulfide is a purely planar–chiral compound (two planar chiral centres), i.e. bis[(2S (p))--2-ethenylferrocen-1-yl]phenylphosphane sulfide, [Fe(2)(C(5)H(5))(2)(C(20)H(17)PS)]. Owing to the stereocentres present, reactions performed on [(Fc(A))(2)(Ph)P]-type compounds strongly favour one ferrocene unit over the other due to diastereoselectivity. Furthermore, we present four related structures where the ferrocene units are not identical [(Fc(A))(Fc(B))(Ph)P]. These are {(2S (p))-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}[(2S (p))-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(22)H(21)O(2)PS)], [(2S (p))-2-ethenylferrocen-1-yl]{(2S (p))-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(S)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(20)H(19)OPS)], {(2S (p))-2-[(1R)-1-(acetyloxy)ethyl]ferrocen-1-yl}{(2S (p))-2-[(1R)-1-hydroxyethyl]ferrocen-1-yl}phenyl-(R)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(22)H(23)O(3)PS)], and {(2S (p))-2-[(1R)-1-benzylamino)ethyl]ferrocen-1-yl}[(2S (p))-2-ethenylferrocen-1-yl]phenyl-(S)-phosphine sulfide, [Fe(2)(C(5)H(5))(2)(C(27)H(26)NPS)]. All of the structures are accessible in one step from known precursors. International Union of Crystallography 2021-02-25 /pmc/articles/PMC7941264/ /pubmed/33664166 http://dx.doi.org/10.1107/S2053229621001996 Text en © Honegger et al. 2021 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Research Papers Honegger, Philipp Roller, Alexander Widhalm, Michael Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes |
title | Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes |
title_full | Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes |
title_fullStr | Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes |
title_full_unstemmed | Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes |
title_short | Synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes |
title_sort | synthesis and characterization of enantiopure planar–chiral phosphorus-linked diferrocenes |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941264/ https://www.ncbi.nlm.nih.gov/pubmed/33664166 http://dx.doi.org/10.1107/S2053229621001996 |
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