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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...

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Autores principales: D’yakonov, Vladimir A, Makhamatkhanova, Alevtina L, Agliullina, Rina A, Dilmukhametova, Leisan K, Tyumkina, Tat’yana V, Dzhemilev, Usein M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
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.
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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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