Results 51 to 60 of about 10,075 (214)

Redox-enabled direct stereoconvergent heteroarylation of simple alcohols

open access: yesNature Communications, 2021
Synthesizing complex structures of high enantiomeric excess from racemic feedstock is an enduring challenge. Here, the authors couple racemic secondary alcohols with pyrroles to form enantioenriched 2-substituted heteroarenes, via a borrowing hydrogen ...
Yongbing Liu   +4 more
doaj   +1 more source

Novel Chiral Switching Ligands for Enantioselective Asymmetric Reductions of Prochiral Ketones

open access: yesMolecules, 2001
The newly developed chiral ligands 1 and 4 show opposite enantioselectivity in the asymmetric reduction of prochiral ketones resulting in the production of either enantiomer depending on the metal complex with high enantiomeric excess.
S. Velmathi   +3 more
doaj   +1 more source

Chiral symmetry breaking and information accumulation in pre-biological protocell evolution

open access: yesScientific Reports
We study a linear evolutionary model based on the two-dimensional distribution of protocells by total enantiomeric excess and the amount of stored information, which they can pass from generation to generation, and without any mutual inhibition.
Konstantin K. Konstantinov   +1 more
doaj   +1 more source

Highly Efficient Lipase-Catalyzed Kinetic Resolution of Chiral Amines

open access: yesCHIMIA, 1994
The lipase Candida antarctica catalyzes the enantioselective acetylation of chiral primary amines, kinetic resolution leading to an enantiomeric excess (ee) of 90–98%.
Manfred T. Reetz, Claus Dreisbach
doaj   +2 more sources

On One Hand: The Optical Sensing of Enantiomeric Excess [PDF]

open access: yesChem, 2019
Download : Download high-res image (220KB) Download : Download full-size image Matt graduated from DeMatha Catholic High School in 2005. He earned his BS degree in chemistry at Texas Southern University while simultaneously playing college football. After spending 2 years as a high school chemistry teacher and coach, he decided to deepen
openaire   +1 more source

Prediction of Enantiomeric Excess in a Combinatorial Library of Catalytic Enantioselective Reactions [PDF]

open access: yesJournal of Combinatorial Chemistry, 2005
A quantitative structure-enantioselectivity relationship was established for a combinatorial library of enantioselective reactions performed by addition of diethyl zinc to benzaldehyde. Chiral catalysts and additives were encoded by their chirality codes and presented as input to neural networks.
João, Aires-de-Sousa, Johann, Gasteiger
openaire   +2 more sources

Calcium(II)-mediated resolution of methyl o-chloromandelate with chiral O,O′-dibenzoyltartaric acid in preparative scale

open access: yesMain Group Metal Chemistry, 2019
We report here the coordination-mediated resolution of methyl o-chloromandelate, which is a key intermediate for clopidogrel, in preparative scale. The reaction of CaO, optically pure (2R, 3R)-O,O′-dibenzoyltartaric acid, and methyl o-chloromandelate in ...
Xu Hong-Wu   +4 more
doaj   +1 more source

Hydroformylation of Vinylferrocene with Rhodium and Platinum Catalysts

open access: yesCHIMIA, 1986
2- and 3-ferrocenylpropionaldehydes (2 and 3) have been prepared by highly regioselective hydroformylation of vinylferrocene (1) using rhodium and platinum catalysts.
László Kollár   +2 more
doaj   +1 more source

Photogenerated Oxetanes as a Gateway to Uphill Cyclopropanation

open access: yesAngewandte Chemie International Edition, EarlyView.
An atom‐economical route to densely functionalized cyclopropanes from furans and photochemically activated aldehydes is enabled by a unique oxetane‐to‐cyclopropane rearrangement. These cyclopropanes can be used to access complex bioactive scaffolds and serve as a platform for asymmetric cyclopropane synthesis.
Tim Köglmeier   +2 more
wiley   +1 more source

Enantioselective desymmetrization of cyclohexadienones via an intramolecular Rauhut–Currier reaction of allenoates

open access: yesNature Communications, 2016
The Rauhut-Currier reaction is a powerful method to form carbon-carbon bonds. Here, the authors report an enantioselective intramolecular variant between alkenes and allenoates, giving access to highly functionalised bicyclic lactones in excellent ...
Weijun Yao   +5 more
doaj   +1 more source

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