<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(30)</volume><submitter>Duflocq S</submitter><pubmed_abstract>One-pot oxime ligation under mild conditions using Pd(ii) as a shared catalyst from an aldehyde precursor (Thz) and a protected aminooxyacetyl group (Proc-Aoa) is reported. Two complementary metal-free protocols using unmasked Aoa-peptide are also described. Acetoxime-peptide can proceed to the desired oxime through an additional transoximation step.</pubmed_abstract><journal>RSC advances</journal><pagination>17681-17685</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9053634</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>One-pot oxime ligation from peptides bearing thiazolidine and aminooxyacetyl groups.</pubmed_title><pmcid>PMC9053634</pmcid><pubmed_authors>Duflocq S</pubmed_authors><pubmed_authors>Huguenot F</pubmed_authors><pubmed_authors>Vidal M</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors><pubmed_authors>Liu WQ</pubmed_authors></additional><is_claimable>false</is_claimable><name>One-pot oxime ligation from peptides bearing thiazolidine and aminooxyacetyl groups.</name><description>One-pot oxime ligation under mild conditions using Pd(ii) as a shared catalyst from an aldehyde precursor (Thz) and a protected aminooxyacetyl group (Proc-Aoa) is reported. Two complementary metal-free protocols using unmasked Aoa-peptide are also described. Acetoxime-peptide can proceed to the desired oxime through an additional transoximation step.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2025-05-18T12:06:46.699Z</modification><creation>2025-04-06T19:14:20.659Z</creation></dates><accession>S-EPMC9053634</accession><cross_references><pubmed>35515616</pubmed><doi>10.1039/d0ra03235b</doi></cross_references></HashMap>