Results 51 to 60 of about 16,892 (273)

Acylation of trans-2-substituted cyclohexanols: the impact of substituent variation on the pyridine-induced reversal of diastereoselectivity

open access: yes, 2015
Diastereoselectivity in chemical reactions can arise from differences in activation energies associated with the reactants, if the process is kinetically controlled.
Sven Hackbusch   +3 more
core   +1 more source

Diastereoselective Transfer Hydrogenation of Cyclic and Bicyclic Ketones over Selected Metal Oxides as Catalysts

open access: yesMolecules
The diastereoselectivity of the liquid- and vapor-phase Catalytic Transfer Hydrogenation (CTH) of cyclic ketones: x-methylcyclohexanones (x = 2, 3 or 4), 4-t-butylcyclohexanone, and bicyclic ketones: 2-norbornanone, camphor, fenchone, and a tricyclic ...
Marek Gliński   +6 more
doaj   +1 more source

A Chiral Saddle‐Shaped Nanographene With Two Heptagon‐Embedded [4]Helicenes

open access: yesAngewandte Chemie International Edition, EarlyView.
We present a novel synthetic strategy toward a chiral saddle‐shaped nanographene (cSNG) via a two‐step oxidation of a prochiral anthracene precursor. The Scholl‐type oxidation first yields a key intermediate with sp3‐defect heptagons, and subsequent oxidative dehydrogenation affords fully conjugated cSNG.
Felix Trautner   +11 more
wiley   +1 more source

Intra- and Intermolecular Diastereoselectivity of 5-Hydroxy-2-adamantylidene

open access: yes, 2016
Intra- and Intermolecular Diastereoselectivity of 5-Hydroxy-2-adamantylidene†
Udo H. Brinker (1470559)   +1 more
core   +1 more source

Additions to Fe(CO)3−Dienal Complexes:  Dependence of Diastereoselectivity on Lewis Acid

open access: yes, 2016
Lewis acid mediated additions to Fe(CO)3−2,4-dienal complexes are explored. Silyl enol ether and allylstannane nucleophiles both undergo aldehyde addition with good diastereoselectivity.
Daniel F. Harvey (3031866)   +1 more
core   +1 more source

Monovalent chiral-at-copper complexes: halide-controlled diastereoselectivity [PDF]

open access: yes, 2012
An unusual example of diastereoselectivity has been observed in Cu(κ3-P,C,P′-1)X complexes where 1 is an asymmetric tridentate ligand containing a bicyclic NHC framework and X is a halide.
Newman, Paul David   +2 more
core   +1 more source

Diastereoselective synthesis of highly substituted cyclohexanones and tetrahydrochromene-4-ones via conjugate addition of curcumins to arylidenemalonates

open access: yesBeilstein Journal of Organic Chemistry
A cascade inter–intramolecular double Michael strategy for the synthesis of highly functionalized cyclohexanones from curcumins and arylidenemalonates is reported. This strategy works in the presence of aqueous KOH using TBAB as a suitable phase transfer
Deepa Nair   +3 more
doaj   +1 more source

diastereoselectivity

open access: yes, 2019
Citation: 'diastereoselectivity' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.D01684 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

Solvent-controlled diastereoselectivity in tryptophan-catalyzed Mannich reactions [PDF]

open access: yes, 2018
Solvent effects in the L-tryptophan-catalyzed Mannich reaction between hydroxyacetone and glyoxylate imines have been examined. The use of a DMSO/1-butanol (4:1 v/v) mixture as solvent at rt provided the expected Mannich adducts in good yields, high anti-
Moyano i Baldoire, Albert   +2 more
core   +1 more source

Predicting the Diastereoselectivity of Rh-Mediated Intramolecular C−H Insertion

open access: yes, 2016
Rhodium-mediated cyclization of the α-diazo ester 1 proceeds with high diastereoselectivity, to give the trisubstituted cyclopentane 5. A computational model (ZINDO and Molecular Mechanics) based on our current mechanistic understanding of the reaction ...
Arnold L. Rheingold (1274736)   +2 more
core   +2 more sources

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