{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Kumar M"],"funding":["European Research Council","Engineering and Physical Sciences Research Council"],"pagination":["16753-16756"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6348375"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["24(63)"],"pubmed_abstract":["The inthomycins are a family of structurally and biologically rich natural products isolated from Streptomyces species. Herein the implementation of a modular synthetic route is reported that has enabled the enantioselective synthesis of all three inthomycins. Key steps include Suzuki and Sonogashira cross-couplings and an enantioselective Kiyooka aldol reaction."],"journal":["Chemistry (Weinheim an der Bergstrasse, Germany)"],"pubmed_title":["Short, Tin-Free Synthesis of All Three Inthomycins."],"pmcid":["PMC6348375"],"funding_grant_id":["708354","EP/J004499/1"],"pubmed_authors":["Anderson Z","Kumar M","Overy A","Burton JW","Bromhead L"],"additional_accession":[]},"is_claimable":false,"name":"Short, Tin-Free Synthesis of All Three Inthomycins.","description":"The inthomycins are a family of structurally and biologically rich natural products isolated from Streptomyces species. Herein the implementation of a modular synthetic route is reported that has enabled the enantioselective synthesis of all three inthomycins. Key steps include Suzuki and Sonogashira cross-couplings and an enantioselective Kiyooka aldol reaction.","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 Nov","modification":"2026-05-07T06:29:22.162Z","creation":"2025-05-29T22:28:48.278Z"},"accession":"S-EPMC6348375","cross_references":{"pubmed":["30338587"],"doi":["10.1002/chem.201803794"]}}