<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(35)</volume><submitter>Iyer MR</submitter><pubmed_abstract>We report the development of a one-pot Bunte's reaction-enabled expeditious platform under aqueous conditions for the scalable conversion of sulfonylureas to synthetically versatile thio-sulfonylureas. The reaction was further propagated in the same pot to yield diverse chiral and achiral isothiosulfonyl analogs. The protocol enabled the synthesis of various drug-like molecules and was applied to an enantiomeric synthesis of a cannabinoid receptor antagonist SLV326.</pubmed_abstract><journal>ACS omega</journal><pagination>31612-31620</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9453971</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>One-Pot Synthesis of Thio-Augmented Sulfonylureas via a Modified Bunte's Reaction.</pubmed_title><pmcid>PMC9453971</pmcid><pubmed_authors>Kundu B</pubmed_authors><pubmed_authors>Bhattacharjee P</pubmed_authors><pubmed_authors>Rutland N</pubmed_authors><pubmed_authors>Iyer MR</pubmed_authors><pubmed_authors>Wood CM</pubmed_authors></additional><is_claimable>false</is_claimable><name>One-Pot Synthesis of Thio-Augmented Sulfonylureas via a Modified Bunte's Reaction.</name><description>We report the development of a one-pot Bunte's reaction-enabled expeditious platform under aqueous conditions for the scalable conversion of sulfonylureas to synthetically versatile thio-sulfonylureas. The reaction was further propagated in the same pot to yield diverse chiral and achiral isothiosulfonyl analogs. The protocol enabled the synthesis of various drug-like molecules and was applied to an enantiomeric synthesis of a cannabinoid receptor antagonist SLV326.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-18T15:35:23.11Z</modification><creation>2025-04-07T02:21:00.733Z</creation></dates><accession>S-EPMC9453971</accession><cross_references><pubmed>36092569</pubmed><doi>10.1021/acsomega.2c04816</doi></cross_references></HashMap>