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The following term was not found in PubMed: jaratjarungkiat
Page 1
Showing results for sulfenate jaratjarungkiat
Your search for Sureenate Jaratjarungkiat retrieved no results
Sulfenate Anion Catalyzed Diastereoselective Synthesis of Aziridines.
Zheng Z, Pu Y, Adrio J, Walsh PJ. Zheng Z, et al. Angew Chem Int Ed Engl. 2023 Jun 19;62(25):e202303069. doi: 10.1002/anie.202303069. Epub 2023 May 9. Angew Chem Int Ed Engl. 2023. PMID: 37068049
Herein, we report a broadly applicable and diastereoselective synthetic method for the synthesis of trans-aziridines from imines and benzylic or alkyl halides utilizing sulfenate anions (PhSO(-) ) as the catalyst. Substrates bearing heterocyclic aromatic groups, alkyl, and …
Herein, we report a broadly applicable and diastereoselective synthetic method for the synthesis of trans-aziridines from imines and benzyli …
Palladium-Catalyzed Arylation of Alkyl Sulfenate Anions.
Jia T, Zhang M, Jiang H, Wang CY, Walsh PJ. Jia T, et al. J Am Chem Soc. 2015 Nov 4;137(43):13887-93. doi: 10.1021/jacs.5b08117. Epub 2015 Oct 27. J Am Chem Soc. 2015. PMID: 26460506
A unique palladium-catalyzed arylation of alkyl sulfenate anions is introduced that affords aryl alkyl sulfoxides in high yields. Due to the base sensitivity of the starting sulfoxides, sulfenate anion intermediates, and alkyl aryl sulfoxide products, the use of a m …
A unique palladium-catalyzed arylation of alkyl sulfenate anions is introduced that affords aryl alkyl sulfoxides in high yields. Due …
Nucleophilic covalent ligand discovery for the cysteine redoxome.
Fu L, Jung Y, Tian C, Ferreira RB, Cheng R, He F, Yang J, Carroll KS. Fu L, et al. Nat Chem Biol. 2023 Nov;19(11):1309-1319. doi: 10.1038/s41589-023-01330-5. Epub 2023 May 29. Nat Chem Biol. 2023. PMID: 37248412
With an eye toward expanding chemistries used for covalent ligand discovery, we elaborated an umpolung strategy that exploits the 'polarity reversal' of sulfur when cysteine is oxidized to sulfenic acid, a widespread post-translational modification, for selective bioconjug …
With an eye toward expanding chemistries used for covalent ligand discovery, we elaborated an umpolung strategy that exploits the 'polarity …
Palladium-Catalyzed Enantioselective Alkenylation of Sulfenate Anions.
Wu C, Berritt S, Liang X, Walsh PJ. Wu C, et al. Org Lett. 2019 Feb 15;21(4):960-964. doi: 10.1021/acs.orglett.8b03943. Epub 2019 Jan 29. Org Lett. 2019. PMID: 30694063
A novel approach to synthesize enantio-enriched alkenyl/aryl sulfoxides is achieved by using CsF to generate sulfenate anions and conducting the catalytic enantioselective alkenylation with [Pd(allyl)Cl](2)/(2 R)-1-[(1 R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(diphen …
A novel approach to synthesize enantio-enriched alkenyl/aryl sulfoxides is achieved by using CsF to generate sulfenate anions and con …
Copper-sulfenate complex from oxidation of a cavity mutant of Pseudomonas aeruginosa azurin.
Sieracki NA, Tian S, Hadt RG, Zhang JL, Woertink JS, Nilges MJ, Sun F, Solomon EI, Lu Y. Sieracki NA, et al. Proc Natl Acad Sci U S A. 2014 Jan 21;111(3):924-9. doi: 10.1073/pnas.1316483111. Epub 2014 Jan 3. Proc Natl Acad Sci U S A. 2014. PMID: 24390543 Free PMC article.
Metal-sulfenate centers are known to play important roles in biology and yet only limited examples are known due to their instability and high reactivity. ...Engineering the electron transfer protein azurin into an active copper enzyme that forms a copper-sulfenate …
Metal-sulfenate centers are known to play important roles in biology and yet only limited examples are known due to their instability …
Peptide synthesis.
Gish D. Gish D. Mol Biol Biochem Biophys. 1970;8:276-335. doi: 10.1007/978-3-662-12834-3_10. Mol Biol Biochem Biophys. 1970. PMID: 4950192 Review. No abstract available.
Advances of Sulfenate Anions in Catalytic Asymmetric Synthesis of Sulfoxides.
Yang L, Wang B, Yin X, Zeng Q. Yang L, et al. Chem Rec. 2022 Mar;22(3):e202100242. doi: 10.1002/tcr.202100242. Epub 2021 Nov 18. Chem Rec. 2022. PMID: 34796593
In recent years, sulfenate anions as key intermediates in enantioselective synthesis have attracted considerable attention. ...This review presents the in situ preparation methods and the recent applications of sulfenate anions in catalytic asymmetric synthesis of c …
In recent years, sulfenate anions as key intermediates in enantioselective synthesis have attracted considerable attention. ...This r …
Sulfenate anions as organocatalysts for benzylic chloromethyl coupling polymerization via C=C bond formation.
Li M, Berritt S, Wang C, Yang X, Liu Y, Sha SC, Wang B, Wang R, Gao X, Li Z, Fan X, Tao Y, Walsh PJ. Li M, et al. Nat Commun. 2018 May 1;9(1):1754. doi: 10.1038/s41467-018-04095-x. Nat Commun. 2018. PMID: 29717123 Free PMC article.
BCCP is catalyzed by organocatalysts not previously employed in polymerization processes (sulfenate anions), which are generated from bench-stable sulfoxide precatalysts. The sulfenate anion promotes an umpolung polycondensation via step-growth propagation cycles in …
BCCP is catalyzed by organocatalysts not previously employed in polymerization processes (sulfenate anions), which are generated from …
Reactivity of Small Oxoacids of Sulfur.
Makarov SV, Horváth AK, Makarova AS. Makarov SV, et al. Molecules. 2019 Jul 30;24(15):2768. doi: 10.3390/molecules24152768. Molecules. 2019. PMID: 31366103 Free PMC article. Review.
Key intermediates in this process are the so-called small oxoacids of sulfur (SOS)-sulfenic HSOH (hydrogen thioperoxide, oxadisulfane, or sulfur hydride hydroxide) and sulfoxylic S(OH)(2) acids. ...It is well-established that sulfoxylic acid has very strong reducing proper …
Key intermediates in this process are the so-called small oxoacids of sulfur (SOS)-sulfenic HSOH (hydrogen thioperoxide, oxadisulfane …
Sulfenate Esters of Simple Phenols Exhibit Enhanced Activity against Biofilms.
Walsh DJ, Livinghouse T, Durling GM, Chase-Bayless Y, Arnold AD, Stewart PS. Walsh DJ, et al. ACS Omega. 2020 Mar 13;5(11):6010-6020. doi: 10.1021/acsomega.9b04392. eCollection 2020 Mar 24. ACS Omega. 2020. PMID: 32226882 Free PMC article.
Some of the phenolic parent compounds are well-studied constituents of plant essential oils, for example, eugenol, menthol, carvacrol, and thymol. The potency of sulfenate ester derivatives was markedly and consistently increased toward both planktonic cells and biofilms. …
Some of the phenolic parent compounds are well-studied constituents of plant essential oils, for example, eugenol, menthol, carvacrol, and t …
1,119 results