<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>D'yakonov VA</submitter><pubmed_abstract>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'PCl2). Hydrogen peroxide oxidation and treatment with S8 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 </pubmed_abstract><journal>Beilstein journal of organic chemistry</journal><pagination>406-12</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4902032</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes.</pubmed_title><pmcid>PMC4902032</pmcid><pubmed_authors>D'yakonov VA</pubmed_authors><pubmed_authors>Agliullina RA</pubmed_authors><pubmed_authors>Dzhemilev UM</pubmed_authors><pubmed_authors>Makhamatkhanova AL</pubmed_authors><pubmed_authors>Tyumkina TV</pubmed_authors><pubmed_authors>Dilmukhametova LK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aluminacyclopentanes in the synthesis of 3-substituted phospholanes and α,ω-bisphospholanes.</name><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'PCl2). Hydrogen peroxide oxidation and treatment with S8 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 </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2025-04-25T19:16:38.824Z</modification><creation>2019-03-27T02:15:47Z</creation></dates><accession>S-EPMC4902032</accession><cross_references><pubmed>27340436</pubmed><doi>10.3762/bjoc.12.43</doi></cross_references></HashMap>