Results 121 to 130 of about 14,649 (249)
Purple‐light activation of aggregated diphenyl disulfide unlocks the photocatalyst‐free racemization of 1‐arylethanols. The resulting sulfur radical process operates under mild conditions and couples with the enzymatic acylation by Candida antarctica lipase B in a photobiocatalytic dynamic kinetic resolution, revealing new opportunities for sulfur ...
Cristina Guolo +2 more
wiley +1 more source
Copper-Catalyzed Enantioselective Synthesis of Chiral Selenium-Based Versatile Synthons. [PDF]
Huang Q +6 more
europepmc +1 more source
Copper‐Catalyzed α‐Carbamoylation of Cyclic β‐Ketoesters
Cu(II) salt‐catalyzed reaction of cyclic β‐ketoesters with isocyanates afforded hitherto inaccessible α‐substituted β,β’‐dicarbonyl amides possessing an all‐carbon quaternary center. A copper‐catalyzed, base‐free α‐carbamoylation of cyclic β‐ketoesters with isocyanates has been developed.
Yihao Shi, Akihiro Sakama, Kazuaki Kudo
wiley +1 more source
Diarylethene‐containing cyclic tubulysin analogues were designed, synthesized, and evaluated as light‐responsive cytotoxic agents. One analogue showed reversible photoswitching, photoregulated tubulin polymerization inhibition, and photoform‐dependent cytotoxicity.
Anna Iampolska +9 more
wiley +1 more source
Catalytic Enantioselective Synthesis of 1,1-Disubstituted Isochromans. [PDF]
Li Z +7 more
europepmc +1 more source
Cyclodextrins are the most often applied chiral selectors in CE enantioseparations. In combination with NMR spectroscopy and molecular modeling, studies for an understanding of chiral recognition underlying enantioseparations have been performed.
Gerhard K. E. Scriba
wiley +1 more source
Enantioselective Synthesis of Spirolactones and Spirolactams Under Low Catalyst Loadings. [PDF]
Saito T, Navarro A, Davies HML.
europepmc +1 more source
Natural compound phosphonothrixin's herbicidal activity resides exclusively in its (S)‐enantiomer, yet existing enantioselective syntheses are cumbersome, and direct chiral LC separation is hampered by the compound's high polarity, lack of aromatic groups, and metal chelation–induced peak tailing.
Mirna Maalouf +8 more
wiley +1 more source
Enantioselective synthesis of configurationally stable [5]helicenes containing 1,2-azaborine units. [PDF]
Olguin C +10 more
europepmc +1 more source
The acyclic mucobromic acid, activated by (1S)‐(+)‐10‐camphorsulfonic acid, afforded the chiral compound 1b, precursor for aza‐Michael addition/elimination on the butenolide yielding tetronamides 2b‐7b. Their relative SRSR configuration was confirmed by the spectrometric methods, DFT calculation and statistical methods.
Kamylla CF Faria +2 more
wiley +1 more source

