Results 91 to 100 of about 26,606 (255)

diastereoselectivity

Citation: 'diastereoselectivity' in the IUPAC Compendium of Chemical Terminology, 5th ed.; International Union of Pure and Applied Chemistry; 2025. Online version 5.0.0, 2025. 10.1351/goldbook.08162 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for
openaire   +1 more source

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

CHIMIA, 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, Urs Gysel, Joachim N. Kinkel   +2 more
doaj   +2 more sources

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

Nature 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, Q. Peng, A. Mekareeya, R. S. Paton, E. A. Anderson   +4 more
doaj   +1 more source

FLP Mediated Conversion of Difluorobenzylalkynes to Fluoroallenyl Oniums via an SN1’ Pathway

Chemistry – A European Journal, EarlyView.
Frustrated Lewis pair (FLP) selective C‒F activation of difluorobenzylalkynes allows the formation of fluoroallenic oniums via an SN1’ substitution pathway. The fluoroallenic onium salts are synthetic precursors that allow subsequent functionalization at allenic and onium positions.
Max Coles, Tianhong Wang, Rubi McLennan, Long Kit Kwan, Bivas Mondal, Chakyu Richard Chan, Rowan D. Young   +6 more
wiley   +1 more source

Nitrooxylation in Organic Synthesis: From Classical Nitrate Ester Formation to Modern Catalytic Strategies

Chemistry – A European Journal, EarlyView.
Nitrooxylation—the installation of nitrate esters (–ONO2) has evolved from classical mixed‐acid protocols to catalytic and mechano‐, flow‐, photo‐, and electrochemical strategies. This review delineates ionic and radical manifolds for C–ONO2 bond formation, emphasizing mechanistic control, selected substrate scope, and selectivity.
Jayanta Dey, Dmitry Katayev
wiley   +1 more source

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

CHIMIA, 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

Scope and mechanism of the highly stereoselective metal-mediated domino aldol reactions of enolates with aldehydes

Beilstein Journal of Organic Chemistry, 2016
A one-pot transformation, which involves the reaction of ketones with aldehydes in the presence of metal halides to furnish tetrahydro-2H-pyran-2,4-diols in a highly diastereoselective manner, is investigated thoroughly by experiments and computations ...
M. Emin Cinar, Bernward Engelen, Martin Panthöfer, Hans-Jörg Deiseroth, Jens Schlirf, Michael Schmittel   +5 more
doaj   +1 more source

Highly Efficient and Diastereoselective Synthesis of New Pyrazolylpyrrolizine and Pyrazolylpyrrolidine Derivates by a Three-Component Domino Process

Molecules, 2014
Diastereoselective reactions between 4-formylpyrazoles, N-substituted maleimides and glycine derivates led to new series of pyrazolyldipyrrolo [3,4-a:3',4'-f]pyrrolizines and pyrazolylpyrrolo[3,4-c]pyrroles in good yields.
Jairo Quiroga, Jaime Gálvez, Rodrigo Abonia, Braulio Insuasty, Alejandro Ortíz, Justo Cobo, Manuel Nogueras   +6 more
doaj   +1 more source

Diastereoselective Total Synthesis of Salvileucalin C

, 2016
A concise and efficient approach for the diastereoselective total synthesis of salvileucalin C, as well as their biosynthetically related diterpenoids salvileucalin D, salvipuberulin, isosalvipuberulin, and dugesin B, has been reported for the first time.
Hanfeng Ding (1743382), Jun Xuan (1546138), Chenchen Fu (1789324), Yuanbao Zhang (394924), Bingnan Wang (1789330), Chenlong Zhu (1789327)   +5 more
core   +1 more source

Stereochemical Control in the Matteson Reaction

Chemistry – A European Journal, EarlyView.
The Matteson homologation is a highly versatile method for the stereoselective insertion of carbenoids into boronic esters. Through iterative application of the process, complex chiral molecules can be synthesized. The stereoselectivity of the reaction is determined by a chiral diol incorporated in the boronic ester.
Hae Mo Lee, Christoph Hirschhäuser
wiley   +1 more source