<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(10)</volume><submitter>Hua G</submitter><pubmed_abstract>A new one-pot preparative route was developed to synthesize novel organophosphorus-sulfur heterocycles via the reaction of the four-membered ring thionation reagent [2,4-diferrocenyl-1,3,2,4-diathiadiphosphetane 2,4-disulfide (FcLR, a ferrocene analogue of Lawesson's reagent)] and alkenyl/aryl-diols and I₂ (or SOCl₂) in the presence of triethylamine. Therefore, a series of five- to ten-membered heterocycles bearing an O-P(S)-O or an O-P(S)-S-S-P(S)-O linkage were synthesized. The synthesis features a novel application of the multicomponent reaction, providing an efficient and environmentally benign method for the preparation of the unusual phosphorus-sulfur heterocycles. Seven representative X-ray structures confirm the formation of these heterocycles.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>E1687</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6151443</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phosphorus-Sulfur Heterocycles Incorporating an O-P(S)-O or O-P(S)-S-S-P(S)-O Scaffold: One-Pot Synthesis and Crystal Structure Study.</pubmed_title><pmcid>PMC6151443</pmcid><pubmed_authors>Slawin AMZ</pubmed_authors><pubmed_authors>Hua G</pubmed_authors><pubmed_authors>Cordes DB</pubmed_authors><pubmed_authors>Du J</pubmed_authors><pubmed_authors>Davidson K</pubmed_authors><pubmed_authors>Woollins JD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phosphorus-Sulfur Heterocycles Incorporating an O-P(S)-O or O-P(S)-S-S-P(S)-O Scaffold: One-Pot Synthesis and Crystal Structure Study.</name><description>A new one-pot preparative route was developed to synthesize novel organophosphorus-sulfur heterocycles via the reaction of the four-membered ring thionation reagent [2,4-diferrocenyl-1,3,2,4-diathiadiphosphetane 2,4-disulfide (FcLR, a ferrocene analogue of Lawesson's reagent)] and alkenyl/aryl-diols and I₂ (or SOCl₂) in the presence of triethylamine. Therefore, a series of five- to ten-membered heterocycles bearing an O-P(S)-O or an O-P(S)-S-S-P(S)-O linkage were synthesized. The synthesis features a novel application of the multicomponent reaction, providing an efficient and environmentally benign method for the preparation of the unusual phosphorus-sulfur heterocycles. Seven representative X-ray structures confirm the formation of these heterocycles.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Oct</publication><modification>2025-04-19T16:19:09.853Z</modification><creation>2019-03-27T00:06:43Z</creation></dates><accession>S-EPMC6151443</accession><cross_references><pubmed>28994745</pubmed><doi>10.3390/molecules22101687</doi></cross_references></HashMap>