Results 51 to 60 of about 3,131,133 (230)

Lattice and thermodynamic characteristics of N-stearoyl-allo-threonine monolayers

open access: yes, 2020
The effect of the second chiral center of diastereomeric N-alkanoyl-allo-threonine on the main monolayer characteristics has been investigated. The characteristic features of the enantiomeric and racemic forms of N-stearoyl-allo-threonine monolayers are ...
Brezesinski, G.   +2 more
core   +1 more source

Asymmetric preparation of antifungal 1-(4 -chlorophenyl)-1-cyclopropyl methanol and 1-(4 -chlorophenyl)-2-phenylethanol. Study of the detoxification mechanism by Botrytis cinerea [PDF]

open access: yes, 2011
Chiral alcohols are important as bioactive compounds or as precursors to such molecules. On the basis of the different antifungal properties of the enantiopure alcohol derivatives of 4-chlorophenyl cyclopropyl ketone and benzyl 4-chlorophenyl ketone ...
Aleu Casatejada, Josefina   +4 more
core   +2 more sources

rac-3-[(Anilino)(naphthalen-2-yl)methyl]thian-4-one

open access: yesActa Crystallographica Section E, 2012
In the title compound, C22H21NOS, the thiopyranone ring adopts a chair-like conformation with the substituent in the axial position. The relative configuration of the racemic compound is 3R,7S according to the numbering scheme used in this publication ...
A. Wahid Mesbah   +3 more
doaj   +1 more source

rac-Ethyl rel-(2R,3R,4S)-4-hydroxy-1,2-dimethyl-5-oxopyrrolidine-3-carboxylate

open access: yesIUCrData, 2023
The asymmetric unit of the title compound, C9H15NO4, consists of a functionalized pyrrolidine ring having an envelope conformation, synthesized as an ethyl ester. The molecule has three chiral centres and crystallized as a racemic mixture. In the crystal,
Fatin Nur Ain Abdul Rashid   +6 more
doaj   +1 more source

rac-18-Methoxycoronaridine hydrochloride

open access: yesActa Crystallographica Section E, 2012
In the crystal structure of the racemic title compound, C22H29N2O3+·Cl−, both NH groups form N—H...Cl hydrogen bonds with the chloride counter-ion, forming translational chains along the a axis.
Martin E. Kuehne, Rory Waterman
doaj   +1 more source

A male-produced aggregation-sex pheromone of the beetle Arhopalus rusticus (Coleoptera: Cerambycidae, Spondylinae) may be useful in managing this invasive species. [PDF]

open access: yes, 2019
The longhorned beetle Arhopalus rusticus (Coleoptera: Cerambycidae, Spondylinae) is a common species in conifer forests of the Northern Hemisphere, but with global trade, it has invaded and become established in New Zealand, Australia, and South America.
McElfresh, J Steven   +4 more
core   +2 more sources

Recent advances in enzymatic and chemical deracemisation of racemic compounds [PDF]

open access: yesChemical Society Reviews, 2013
Deracemisation of racemic compounds is still the most important strategy to produce optically pure compounds despite many recent advances in asymmetric synthesis. Especially deracemisation approaches that give rise to single enantiomers are preferred, which can be achieved either by invoking organocatalysts, metal complexes or enzymes - leading to ...
Rachwalski, M.   +2 more
openaire   +4 more sources

N-Phenyladamantane-1-sulfinamide

open access: yesActa Crystallographica Section E, 2008
In the racemic title compound, C16H21NOS, the molecules are packed into polymeric chains in the b-axis direction and are linked along the b axis by N—H...O and C—H...O hydrogen bonds.
Mrityunjoy Datta   +3 more
doaj   +1 more source

(2SR,4aSR,8aSR)-6-Oxoperhydronaphthalene-2-carboxylic acid

open access: yesActa Crystallographica Section E, 2009
In the title racemic compound, C11H16O3, the molecule adopts a conformation that places its carboxyl group in an equatorial position. Molecules aggregate by hydrogen-bond pairing of carboxyl groups, yielding centrosymmetric dimers that are arranged into ...
Georgia Efthimiopoulos   +3 more
doaj   +1 more source

Intermolecular interactions in the chiral and racemic forms of 3-hydroxy-2-(1-oxoisoindolin-2-yl)butanoic acid derived from threonine [PDF]

open access: yes, 2000
The title compounds, C₁₂H₁₃NO₄, are derived from L-threonine and DL-threonine, respectively. Hydrogen bonding in the chiral derivative, (2S/3R)-3-hydroxy-2-(1-oxoisoindolin-2-yl)butanoic acid, consists of O-Hacid...Oalkyl-H...O=Cindole chains [O...O 2 ...
Brady, Fiona   +2 more
core   +1 more source

Home - About - Disclaimer - Privacy