Results 191 to 200 of about 13,012 (246)
Lifecycle design of synthetic polymers: toward recyclability and sustainability. [PDF]
Xie T, Men Y.
europepmc +1 more source
Inverse stable isotopic labeling for natural product characterization and discovery.
Robes JMD, Puri AW.
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N- to C-Peptide Synthesis, Arguably the Future for Sustainable Production. [PDF]
Ghosh K, Lubell WD.
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Collective Asymmetric Total Syntheses of Musellarins A-E. [PDF]
Liu Y, Ou Y, Chang V, Yao H, Tong R.
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Making Blank Faces Expressive: Chemical Approaches to the Modification of Chemically Inert Peptides. [PDF]
Moriyama Y, Sada H, Nanjo T.
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Epimerization of Cypermethrin Stereoisomers in Alcohols
Journal of Agricultural and Food Chemistry, 2009Isomerization induced by light, heat, and organic solvents has been shown to occur for some pyrethroid insecticides. Alcohols are popular solvents that are used in sample extraction, storage, and analysis. Thus, alcohol-induced epimerization may contribute to the incorrect interpretation of results from enantioselective chemical analysis and bioassay ...
Daniel Schlenk +2 more
exaly +3 more sources
The epimerization of peptide aldehydes—a systematic study
Journal of Peptide Science, 2006AbstractPeptide aldehydes are interesting targets as enzyme inhibitors, and can be used for pseudopeptide chemistry or ligation. However, they are known to be subjected to epimerization during synthesis or purification. By 1H NMR, a model dipeptide aldehyde can be used to check the possible epimerization occurring during synthesis. Various purification
Matheo Berthet, Jean-Alain Fehrentz
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Functional Characterization and Crystal Structure of the Bifunctional Thioesterase Catalyzing Epimerization and Cyclization in Skyllamycin Biosynthesis [PDF]
The d-amino acid residues are hallmark building blocks of nonribosomal peptides. Here, we report the bifunctional thioesterase domain (TE domain) Skyxy-TE that catalyzes both epimerization and cyclization in skyllamycin biosynthesis.
Ming Ma, Suwei Dong, Liangren Zhang
exaly +2 more sources
The Epimerization of Sesamin and Asarinin
Journal of Natural Products, 2005Sesamin (1) and asarinin (2) are two C-7' epimeric lignans. Molecular modeling by semiempirical methods indicated that 1 is more stable than 2 by about 2.5 kcal/mol. However, epimerization under acidic conditions led to a 44.8/55.2 equilibrium ratio of 1 and 2.
Chia-Ying, Li +2 more
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