Results 141 to 150 of about 39,817 (294)
Stereocontrol in Conformationally Stable C(sp2)─C(sp3) Atropisomers
Building in our expertize in the synthesis of trans‐dihydrobenzofurans via organocatalyzed domino Michael/O‐cyclization between β‐naphthols and nitroalkenes, we developed an efficient strategy to access a new family of atropisomers bearing a conformationally stable C(sp2)─C(sp3) bond and two stereogenic centers through simple and highly ...
Antoine Domain+10 more
wiley +2 more sources
Aziridination of alkenes is an important route to chiral nitrogen‐containing building blocks. We report that carbamate‐functionalized allylic alcohols undergo highly enantioselective aziridination using achiral dimeric Rh complexes ion‐paired with cinchona alkaloid‐derived chiral cations.
Arthur R. Lit+4 more
wiley +2 more sources
Hexabromocyclododecanes (HBCDs) are globally produced brominated flame retardant (BFR) and are used primarily as an additive FR in thermal insulation building materials, upholstery textiles, and electronics.
TIAN Qin+5 more
doaj +1 more source
Catalyst screening without catalysis. By combining cyclic voltammetry and DFT calculations we were able to identify a highly active catalyst for the radical arylation of epoxides without performing any reactions. The prevention of chloride binding that leads to catalyst inhibition was established as the key structural feature.
Niklas Schmickler+6 more
wiley +2 more sources
The chiral pesticide hexythiazox was extensively employed in agricultural activities and has garnered growing concern for its harmful impact on the ecosystem.
Ningying Song+5 more
doaj
Asymmetric Intramolecular α‐Arylation of Polar Amino Acids Bearing β‐Leaving Groups
Use of enolate chemistry to functionalise amino acids with β‐heteroatom side‐chains (serine, cysteine, threonine, etc.) is hampered by β‐elimination. We show that α‐arylation can be achieved by incorporating the side chain into a saturated heterocycle, making the unwanted elimination a disfavoured 5‐endo‐trig reaction.
Ömer Taspinar+6 more
wiley +2 more sources
Summary: Optically active α-quaternary amino acids have received much attention because of the important biomedical applications implicated for compounds containing this structure.
Chao-Yang Zhao+5 more
doaj
Structural shaping of a highly reactive chiral Mn‐oxo species translates into exceptionally enantioselective C─H oxidation catalyst of cyclohexyl 1,3‐meso diethers (up to >99% ee) leading to polyfunctionalized cyclohexanes. Abstract Chiral polyoxygenated cyclohexanes are valuable constituents of biologically relevant products.
Andrea Palone+7 more
wiley +2 more sources
Rapid Access to an Enantioenriched Spiro Bisindole Directly from Indole and Acetone
A catalytic enantioselective one‐pot “self‐assembly” strategy was developed for the exceedingly convenient access to a spiro bisindole directly from indole and acetone. The obtained enantiopure C2‐symmetric bisindole showed exceptional performance as a chiral backbone of diverse effective catalysts or ligands. Abstract Disclosed here is a “one‐pot self‐
Jing‐Yi Wang+3 more
wiley +2 more sources
Catalytic enantioselective synthesis of quaternary carbon stereocentres. [PDF]
Quaternary carbon stereocentres-carbon atoms to which four distinct carbon substituents are attached-are common features of molecules found in nature. However, before recent advances in chemical catalysis, there were few methods of constructing single ...
Overman, Larry E, Quasdorf, Kyle W
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