{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Carrillo AK"],"funding":["NIAID NIH HHS"],"pagination":["1034-7"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC4096711"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["14(4)"],"pubmed_abstract":["A chemical synthesis of the D-ring of mersacidin is reported. The synthetic route relied upon development of a method for late-stage introduction of an unusual S-[(Z)-2-aminovinyl]-(3S)-3-methyl-D-cysteine (AviMeCys) functional group via an oxidative decarbonylation/decarboxylation reaction."],"journal":["Organic letters"],"pubmed_title":["Synthesis of the AviMeCys-containing D-ring of mersacidin."],"pmcid":["PMC4096711"],"funding_grant_id":["R21 AI059327","AI 059327","R01 AI059327"],"pubmed_authors":["VanNieuwenhze MS","Carrillo AK"],"additional_accession":[]},"is_claimable":false,"name":"Synthesis of the AviMeCys-containing D-ring of mersacidin.","description":"A chemical synthesis of the D-ring of mersacidin is reported. The synthetic route relied upon development of a method for late-stage introduction of an unusual S-[(Z)-2-aminovinyl]-(3S)-3-methyl-D-cysteine (AviMeCys) functional group via an oxidative decarbonylation/decarboxylation reaction.","dates":{"release":"2012-01-01T00:00:00Z","publication":"2012 Feb","modification":"2025-04-22T01:02:38.715Z","creation":"2019-03-27T01:32:00Z"},"accession":"S-EPMC4096711","cross_references":{"pubmed":["22296295"],"doi":["10.1021/ol2034806"]}}