<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Blackburn JM</submitter><funding>NIGMS NIH HHS</funding><pagination>6012-6015</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5716482</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(21)</volume><pubmed_abstract>A general approach to access sulfamate esters through preparation of sulfamic acid salts, subsequent activation with triphenylphosphine ditriflate, and nucleophilic trapping is disclosed. The method proceeds in modest to excellent yields to incorporate nucleophiles derived from aliphatic alcohols and phenols. This approach can be employed to furnish differentially substituted sulfamides.</pubmed_abstract><journal>Organic letters</journal><pubmed_title>Synthesis of N-Substituted Sulfamate Esters from Sulfamic Acid Salts by Activation with Triphenylphosphine Ditriflate.</pubmed_title><pmcid>PMC5716482</pmcid><funding_grant_id>T32 GM007105</funding_grant_id><pubmed_authors>Ayer SK</pubmed_authors><pubmed_authors>Blackburn JM</pubmed_authors><pubmed_authors>Roizen JL</pubmed_authors><pubmed_authors>Short MA</pubmed_authors><pubmed_authors>Muellers TD</pubmed_authors><pubmed_authors>Castanheiro T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis of N-Substituted Sulfamate Esters from Sulfamic Acid Salts by Activation with Triphenylphosphine Ditriflate.</name><description>A general approach to access sulfamate esters through preparation of sulfamic acid salts, subsequent activation with triphenylphosphine ditriflate, and nucleophilic trapping is disclosed. The method proceeds in modest to excellent yields to incorporate nucleophiles derived from aliphatic alcohols and phenols. This approach can be employed to furnish differentially substituted sulfamides.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Nov</publication><modification>2020-10-29T12:45:29Z</modification><creation>2019-03-27T00:04:54Z</creation></dates><accession>S-EPMC5716482</accession><cross_references><pubmed>29048913</pubmed><doi>10.1021/acs.orglett.7b03059</doi></cross_references></HashMap>