Results 91 to 100 of about 23,776 (268)

Diastereoselective congested β-amido ketone synthesis via NHC-catalyzed radical–radical coupling

open access: yes, 2023
N-Heterocyclic carbene catalysis merging with photoredox PCET enabled amidoacylation of alkenes to construct sterically congested cyclic β-amido ketone skeleton bearing α-tertiary or quaternary carbon centers with high diastereoselectivity.
Takanori , Matsui   +4 more
core   +1 more source

N‐Aryl Acridone Derivatives as Effective Catalysts for Energy Transfer Reactions

open access: yesChemistry – A European Journal, EarlyView.
Acridones derivatives have high triplet energy, are simple accessible, and could be used in challenging [2+2] ENT reactions. ABSTRACT Organic photocatalysts capable of promoting high‐energy triplet energy transfer (EnT) remain limited, particularly for demanding [2+2] photocycloaddition reactions.
Francesco Calogero   +8 more
wiley   +1 more source

Computational ligand design in enantio- and diastereoselective ynamide [5+2] cycloisomerization

open access: yesNature Communications, 2016
Using a chiral catalyst to override the innate stereochemical outcome of a diastereoselective process is a challenging task. Here, the authors use theory and experiment to develop a cycloisomerization where the enantioselectivity is driven by the ...
R. N. Straker   +4 more
doaj   +1 more source

Highly Diastereoselective Alkylation of 3-Substituted Tetrahydroisoquinolines

open access: yes, 2016
Highly Diastereoselective Alkylation of 3-Substituted ...
Sabine Laschat (1642789)   +3 more
core   +1 more source

Flipping the Card With Enantiodivergent Organocatalysis

open access: yesChemistry – A European Journal, EarlyView.
This minireview elaborates on recent organocatalytic strategies for achieving enantiodivergence—the ability to access both product enantiomers using a single chiral catalyst. It highlights how achiral stimuli, such as solvent polarity and chemical additives, along with minimal catalyst modifications, trigger stereochemical inversions in reactions ...
Debora Iapadre   +3 more
wiley   +1 more source

Formal Synthesis of (±)-Coriolin by Diastereocontrolled Nickel(0)-Catalyzed 'Metallo-ene-type' Cyclization/Methoxycarbonylation

open access: yesCHIMIA, 1992
Bicyclooctanone (±)-2, an advanced intermediate for the synthesis of (±)-coriolin, has been synthesized in ten steps starting from 2,2-dimethylpent-4-enal (7). The key step 6 ?
Wolfgang Oppolzer, Akira Ando
doaj   +2 more sources

Hoch effiziente, präparative chromatographische Enantiomerentrennung von 2-Phenyl-1,3-dioxin-4-onen an Cellulose-triacetat und Cuprat-Additionen zu ?-Hydroxycarbonsäure-Derivaten

open access: yesCHIMIA, 1991
The 2-Phenyl-dioxinones 1 and 2 are resolved on cellulose-triacetate columns (medium pressure, eluent MeOH, separation factors ? = 2.0–2.3, injection of g amounts).
Dieter Seebach   +2 more
doaj   +2 more sources

Brønsted-Acid Catalyzed Diastereoselective Synthesis of Spiroisoindolinones from Enamides

open access: yes
A highly diastereoselective synthesis of spiroisoindolinones from enamides and 3-hydroxy-isoindolinones is reported. The reaction proceeds rapidly in the presence of para-toluenesulfonic acid as Brønsted acid-catalyst and affords a variety of densely ...
Miro , Halaczkiewicz   +3 more
core   +1 more source

Covalent Insertion of a Mn(Salen) Type Complex in Cross‐Linked Protein Crystals: Design of an Enantioselective Artificial Epoxidase

open access: yesChemistry – A European Journal, EarlyView.
An Artificial metalloenzyme was designed by a Michael addition between a MnSalen complex and a cysteine residue within NikA crystals. The heterogeneous catalyst was found capable of an enantioselective and stereospecific epoxidation of cis‐β‐methylstyrene in cristallo.
Manel Boukhallat   +8 more
wiley   +1 more source

Titanium‐Catalyzed Diastereoselective Keto‐ and Iminonitrile Cyclizations

open access: yesChemistry – A European Journal, EarlyView.
The titanium(III)‐catalyzed diastereoselective cyclization of readily‐available substituted ketonitriles gives cyclopentanones in good yield and stereoselectivity. Subsequent 1,2‐addition allows the preparation of cyclopentyls with three consecutive stereocenters.
Christoph Kern   +4 more
wiley   +1 more source

Home - About - Disclaimer - Privacy