Results 111 to 120 of about 23,430 (289)

Crystal structure of 2-chloro-1-(3-ethyl-2,6-diphenylpiperidin-1-yl)ethanone

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2015
In the racemic title compound, C21H24ClNO, the dihedral angle between the planes of the benzene rings is 86.52 (14)° and those between the benzene rings and the piperidine ring are 61.66 (14) and 86.39 (14)°.
V. Shreevidhyaa Suressh   +4 more
doaj   +1 more source

Crystallization of the Racemic Conglomerate and Racemic Compound of Efonidipine [PDF]

open access: yesProceedings of the 2016 International Conference on Biological Engineering and Pharmacy (BEP 2016), 2017
Wen LI   +3 more
openaire   +1 more source

(1aR*,2R*,7S*,7aS*)-rel-3,6-Dimethoxy-2-methyl-1a,2,7,7a-tetrahydro-2,7-epoxy-1H-cyclopropa[b]naphthalene

open access: yesIUCrData, 2016
In the racemic title compound, C14H16O3, the dihedral angle formed by the mean planes of the cyclopropane and benzene rings is 5.0 (2)°. In the crystal, a pair of weak C—H...O hydrogen bonds connect two molecules related by a twofold rotation axis, thus ...
Alan J. Lough   +2 more
doaj   +1 more source

Unraveling hidden symmetry breaking in racemic compounds

open access: yesProceedings of the National Academy of Sciences
Racemic compounds, consisting of an equimolar mixture of enantiomers in crystalline form, are conventionally regarded as fully symmetric and are often dismissed as a trivial phenomenon due to their abundance—as they account for a substantial fraction (90 to 95%) of entries in structural databases.
Weihao Wang   +5 more
openaire   +3 more sources

Application of crystallization inhibitors to chiral separations. 1. Design of additives to discriminate between the racemic compound and the pure enantiomer of mandelic acid

open access: yes, 2007
In the context of the potential use of crystallization for spontaneous separation of racemates, it is well-known that the frequent appearance of racemic solid forms (racemic compounds) is a serious obstacle.
Davey, R. J.; id_orcid   +2 more
core   +1 more source

(Acetato-κ2O,O′)[2′-(di-tert-butylphosphanyl)-1,1′-biphenyl-κ2P,C2]palladium(II)

open access: yesActa Crystallographica Section E, 2012
The structure of the title compound, [Pd(C2H3O2)(C20H26P)], shows a distorted square-planar geometry for the PdII atom, with significant deviations being evident owing to the asymmetric coordination mode of the acetate ligand. A weak intramolecular C&
Charmaine Arderne, Cedric W. Holzapfel
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

Synthesis and Biological Evaluation of Benzochromenopyrimidinones as Cholinesterase Inhibitors and Potent Antioxidant, Non-Hepatotoxic Agents for Alzheimer’s Disease

open access: yesMolecules, 2016
We report herein the straightforward two-step synthesis and biological assessment of novel racemic benzochromenopyrimidinones as non-hepatotoxic, acetylcholinesterase inhibitors with antioxidative properties.
Youssef Dgachi   +14 more
doaj   +1 more source

Toward Continuous Deracemization via Racemic Crystal Transformation Monitored by in Situ Raman Spectroscopy

open access: yes, 2019
In this work, we demonstrate a semibatch solid-state deracemization process for N-(2-chlorobenzylidene)­henylglycine amide­ (NCPA), a complex chiral polymorphic system that involves three types of crystalline racemates (racemic compound and conglomerate ...
Raghunath Venkatramanan (7349708)   +15 more
core   +1 more source

Preferential crystallization of a racemic compound via its conglomerate co-crystals

open access: yes, 2016
Preferential crystallization, as a powerful chiral resolution technique, is intrinsically limited to chiral molecules that crystallize as conglomerates.
Villamil Ramirez, O.F. (author)
core  

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