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Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes
An efficient one-pot process for the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes was developed. The method involves the replacement of aluminium in aluminacyclopentanes, prepared in situ by catalytic cycloalumination of α-olefins and α,ω-diolefins, by phosphorus atoms on treatmen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902032/ https://www.ncbi.nlm.nih.gov/pubmed/27340436 http://dx.doi.org/10.3762/bjoc.12.43 |
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author | D’yakonov, Vladimir A Makhamatkhanova, Alevtina L Agliullina, Rina A Dilmukhametova, Leisan K Tyumkina, Tat’yana V Dzhemilev, Usein M |
author_facet | D’yakonov, Vladimir A Makhamatkhanova, Alevtina L Agliullina, Rina A Dilmukhametova, Leisan K Tyumkina, Tat’yana V Dzhemilev, Usein M |
author_sort | D’yakonov, Vladimir A |
collection | PubMed |
description | An efficient one-pot process for the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes was developed. The method involves the replacement of aluminium in aluminacyclopentanes, prepared in situ by catalytic cycloalumination of α-olefins and α,ω-diolefins, by phosphorus atoms on treatment with dichlorophosphines (R′PCl(2)). Hydrogen peroxide oxidation and treatment with S(8) of the synthesized phospholanes and α,ω-bisphospholanes afforded the corresponding 3-alkyl(aryl)-1-alkyl(phenyl)phospholane 1-oxides, 3-alkyl(aryl)-1-alkyl(phenyl)phospholane 1-sulfides, bisphospholane 1,1'-dioxides, and bisphospholane 1,1'-disulfides in nearly quantitative yields. The complexes LMo(CO)(5) (L = 3-hexyl-1-phenylphospholane, 3-benzyl-1-methylphospholane, 1,2-bis(1-phenylphospholan-3-yl)ethane, and 1,6-bis(1-phenylphospholan-3-yl)hexane were prepared by the reaction of 3-substituted phospholanes and α,ω-bisphospholanes with molybdenum hexacarbonyl. The structure of the complexes was proved by multinuclear (1)H, (13)C, and (31)P spectroscopy. |
format | Online Article Text |
id | pubmed-4902032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-49020322016-06-23 Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes D’yakonov, Vladimir A Makhamatkhanova, Alevtina L Agliullina, Rina A Dilmukhametova, Leisan K Tyumkina, Tat’yana V Dzhemilev, Usein M Beilstein J Org Chem Full Research Paper An efficient one-pot process for the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes was developed. The method involves the replacement of aluminium in aluminacyclopentanes, prepared in situ by catalytic cycloalumination of α-olefins and α,ω-diolefins, by phosphorus atoms on treatment with dichlorophosphines (R′PCl(2)). Hydrogen peroxide oxidation and treatment with S(8) of the synthesized phospholanes and α,ω-bisphospholanes afforded the corresponding 3-alkyl(aryl)-1-alkyl(phenyl)phospholane 1-oxides, 3-alkyl(aryl)-1-alkyl(phenyl)phospholane 1-sulfides, bisphospholane 1,1'-dioxides, and bisphospholane 1,1'-disulfides in nearly quantitative yields. The complexes LMo(CO)(5) (L = 3-hexyl-1-phenylphospholane, 3-benzyl-1-methylphospholane, 1,2-bis(1-phenylphospholan-3-yl)ethane, and 1,6-bis(1-phenylphospholan-3-yl)hexane were prepared by the reaction of 3-substituted phospholanes and α,ω-bisphospholanes with molybdenum hexacarbonyl. The structure of the complexes was proved by multinuclear (1)H, (13)C, and (31)P spectroscopy. Beilstein-Institut 2016-03-02 /pmc/articles/PMC4902032/ /pubmed/27340436 http://dx.doi.org/10.3762/bjoc.12.43 Text en Copyright © 2016, D’yakonov et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper D’yakonov, Vladimir A Makhamatkhanova, Alevtina L Agliullina, Rina A Dilmukhametova, Leisan K Tyumkina, Tat’yana V Dzhemilev, Usein M Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes |
title | Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes |
title_full | Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes |
title_fullStr | Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes |
title_full_unstemmed | Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes |
title_short | Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes |
title_sort | aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902032/ https://www.ncbi.nlm.nih.gov/pubmed/27340436 http://dx.doi.org/10.3762/bjoc.12.43 |
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