Top Tweets for #thioesters
In a new study published in @OrgBiomolChem, #TUS scientists develop a new #efficient #synthesis route to produce #SulfinateEsters, a type of #organosulfur compound, using #thioesters.
Issue 11: Cover: #Rh-catalysis (Cui, Wu); Reviews: C-H functionalization of #heterocycles (Krylov, Terent'ev), 3-membered rings (Li, Jin); #OA: unsaturated #thioesters (Kudo), diazomethanes (Schembri, Odell), #photobiocatalysis (Lavandera,Gotor-Fernández): https://t.co/4LiBvT1CP9
Direct Synthesis of Thioesters from Feedstock Chemicals and Elemental Sulfur @ChemNUS @NUSingapore @TotalSynthesis #Thioesters #Feedstock #Sulfur https://t.co/QTiM4xV0FJ
Enzyme-Responsive Peptide Thioesters for Targeting Golgi Apparatus @BrandeisInquiry @BrandeisU @brandeischem #Enzyme #Peptide #Thioesters #Golgi https://t.co/nv2G7ushft
Yahui Li et al. report a mild, efficient, functional group tolerant, and highly #chemoselective N-acylation of #indoles using #thioesters as a stable acyl source.
🔗 https://t.co/loiuxi5FHi
#DiamondOpenAccess 💎🔓 in the #BJOC – no fees for authors and readers!
#decarbonylations #crosscoupling Check out our recent method for decarbonylative #aryl #exchange between #amides & #thioesters with Chengwei Liu’s group @ChengweiGood #thioether synthesis using #palladium in the absence of nucleophilic thiols. @JOC_OL
https://t.co/cN0UMTNt9x
#decarbonylations #thioethers Check out our recent concept on #decarbonylative C–S #bond synthesis. #Thioesters as a novel & orthogonal class of substrates for the synthesis of #thioethers! @ChengweiGood @ChemCatChem
https://t.co/ElWwsvUciI
Just accepted communication by Xiao-Feng Wu and co-authors: #Palladium‐Catalyzed Thiocarbonylation of Benzyl #Chlorides with #Sulfonyl Chlorides for the Synthesis of Arylacetyl #Thioesters https://t.co/NgZ7P65Fwp
💡 Realizing that unprotected peptide #thioesters react chemoselectively with unprotected N-terminal cysteine residues to form amide linkages was an important advancement in #proteinsynthesis. Check out Stephen Kent's results in SYNFACTS: https://t.co/b5N3vsfAcj @scrippsresearch
Wang and co-workers @BIO5 @UofA report the #organocatalytic transformation of aldehydes to #thioesters by using #VisibleLight https://t.co/202rAaAKMU
@Wiley_Chemistry Sulfur 🤗 as it the essential atom in #thiols for adsorption at metals and useful handles in peptides, as well as in #thioesters, versatile compounds in chemistry and much more exciting in biochemistry #acetyl-CoA
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