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Asymmetric Catalysis [PDF]

open access: hybridProceedings of the National Academy of Sciences, 2004
The demand for chiral compounds, often as single enantiomers, has escalated sharply in recent years, driven particularly by the demands of the pharmaceutical industry, but also by other applications, including agricultural chemicals, flavors, fragrances, and materials.
Barry M. Trost, Jack Halpern
openaire   +4 more sources

Multifunctional Asymmetric Catalysis.

open access: bronzeChemical and Pharmaceutical Bulletin, 2001
Two types of general and practical enantioselective catalysts, namely, bimetallic complexes and Lewis acid-Lewis base bifunctional catalysts were developed based on the concept of multifunctional catalysis. In the first part of this review, the first example of a catalytic enatioselective nitro-Mannich reaction as well as a direct catalytic ...
Motomu Kanai, Masakatsu Shibasaki
openaire   +4 more sources

A unified machine-learning protocol for asymmetric catalysis as a proof of concept demonstration using asymmetric hydrogenation. [PDF]

open access: yesProc Natl Acad Sci U S A, 2020
Significance Development of suitable machine-learning (ML) approaches by using molecular descriptors can provide significant impetus to current efforts in asymmetric catalysis, wherein one strives to make a desired stereoisomer of a given handedness ...
Singh S   +6 more
europepmc   +2 more sources

Ultra-high-throughput mapping of the chemical space of asymmetric catalysis enables accelerated reaction discovery [PDF]

open access: yesNature Communications, 2023
The discovery of highly enantioselective catalysts and elucidating their generality face great challenges due to the complex multidimensional chemical space of asymmetric catalysis and inefficient screening methods.
Wenjing Nie   +5 more
doaj   +2 more sources

Cooperative Photoredox and Asymmetric Catalysis

open access: yesCHIMIA, 2016
Chemical processes combining visible-light-activated redox catalysis with asymmetric catalysis are reviewed, including enamine catalysis in the presence or absence of an additional photoredox sensitizer, phase transfer catalysis exploiting an in
Haohua Huo, Eric Meggersa
doaj   +5 more sources

Synthesis of Homochiral N‐Heterocyclic Carbene‐Based Nanosheets for Enhanced Asymmetric Catalysis [PDF]

open access: yesAdvanced Science
Utilizing ultrathin 2D metal–organic framework nanosheets (2D MONs) as supports for incorporating chiral catalysts represents a highly promising avenue in the field of asymmetric catalysis.
Xinchao Wang   +6 more
doaj   +2 more sources

Asymmetric 1,4-functionalization of 1,3-enynes via dual photoredox and chromium catalysis

open access: yesNature Communications, 2022
In contrast to the better-studied ionic pathway, radical-involved asymmetric 1,4-functionalization of 1,3-enynes remains a prominent challenge. Here, the authors describe the asymmetric three-component 1,4-dialkylation of 1,3-enynes via dual photoredox ...
Feng-Hua Zhang   +3 more
doaj   +2 more sources

Photothermal conversion triggered thermal asymmetric catalysis within metal nanoparticles loaded homochiral covalent organic framework

open access: yesNature Communications, 2019
Achieving both high stereoselectivity and yield is a challenge for conventional asymmetric catalysis. Here, the authors report two metal nanoparticle-loaded and porphyrin-containing homochiral covalent organic framework-based composite catalysts that ...
Hui-Chao Ma   +3 more
doaj   +2 more sources

Strategies in asymmetric catalysis [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2017
Tehshik P. Yoon
doaj   +3 more sources

Synthesis of novel phthalimido oxime pseudoesters and evaluation of their cytotoxicity [PDF]

open access: yesJournal of the Serbian Chemical Society, 2020
A series of novel optically pure oxime pseudoesters derivatives were synthesized by the reaction of substitute keto oximes with various N-substituted α-amino acids chlorides in the presence of triethylamine and dichloromethane at 0°C, and their ...
Mehrez Asma   +4 more
doaj   +1 more source

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