Results 41 to 50 of about 736,450 (179)

Chapter As in trans art

open access: yes, 2023
This article engages with trans artistic practices: both trans in art as well as trans as art. It takes as its point of departure the artistic work of Ro Robertson, Tama Sharman, and Erica Rutherford, each of whom works with trans in different ways.
Hettinga, Lieks   +2 more
core   +1 more source

(2E,4E)-1-(2-Hydroxyphenyl)-5-phenylpenta-2,4-dien-1-one

open access: yesActa Crystallographica Section E, 2011
In the structure of the title chalcone, C17H14O2, derived from cinnamaldehyde, the olefine group has a trans configuration. The molecular conformation is stabilized by an intramolecular O—H...O hydrogen-bond interaction with graph-set motif S(6)
W. A. Silva, C. C. Gatto, G. R. Oliveira
doaj   +1 more source

Chalcone-Thiazole Hybrids: Rational Design, Synthesis, and Lead Identification against 5‑Lipoxygenase

open access: yes, 2019
A hybrid pharmacophore approach is used to design and synthesize novel chalcone-thiazole hybrid molecules. Herein, thiazole has been hybridized with chalcone to obtain a new class of 5-LOX inhibitors.
Mukesh Doble (412086)   +2 more
core   +1 more source

(E)-3-{4,6-Dimethoxy-2-[(E)-4-methoxystyryl]-3-methylphenyl}-1-(2-hydroxy-5-methoxyphenyl)prop-2-en-1-one

open access: yesIUCrData, 2020
In the title compound, C28H28O6, the benzene rings in the resveratrol moiety are connected by a trans C=C double bond, and the hydroxyl group containing a benzene ring and the central benzene ring are linked through a C=(O)—C=C (enone) moiety to form a ...
Miri Yoo, Dongsoo Koh
doaj   +1 more source

Apple scar skin viroid causes dapple and scar skin apple diseases by disrupting phenylpropanoid‐mediated metabolic pathways

open access: yesNew Plant Protection, EarlyView.
Dapple apple and scar skin apple diseases are closely associated with suppression of anthocyanin biosynthesis and enhancement of suberin biosynthesis. Apple scar skin viroid (ASSVd) infection represses anthocyanin biosynthesis in apple callus. Abstract Apple scar skin viroid (ASSVd) causes dapple and scar skin apple diseases, posing serious threats to ...
Lingzhu He   +9 more
wiley   +1 more source

Strategies Toward Accessing Enantioenriched (Hetero)Benzo‐Fused 5‐ and 6‐ Membered Rings via Intermolecular Carbometalation

open access: yesAngewandte Chemie, Volume 138, Issue 23, 1 June 2026.
The use of transition‐metal catalysts and design of chiral ligands have allowed chemists to access highly functionalized benzofused 5‐ and 6‐ membered rings in high yield and enantioselectivity. A common strategy used relies on an intermolecular carbometalation across alkynes and olefins, usually followed by a subsequent intramolecular carbometalation.
Clara Jans   +3 more
wiley   +2 more sources

Crystal structure of (E)-3-(2-hydroxy-4-methylphenyl)-1-(2,4,6-trimethoxyphenyl)prop-2-en-1-one

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2019
The title chalcone derivative, C19H20O5, adopts a trans configuration with respect to the olefinic C=C double bond. The 2-hydroxy-4-methylphenyl ring is coplanar with the attached enone bridge [torsion angle = −179.96 (14)°], where this plane is nearly ...
Maadh Jumaah   +2 more
doaj   +1 more source

Natural Products as Modulators of ABC Transporters in Breast Cancer

open access: yesPhytotherapy Research, EarlyView.
ABSTRACT Breast cancer remains a significant global health challenge, with high incidence and mortality rates despite advancements in early detection and treatment. Multidrug resistance (MDR), particularly in aggressive subtypes like triple‐negative breast cancer (TNBC), continues to hinder effective therapy.
Yoganishalini Sagadevan   +2 more
wiley   +1 more source

Synthesis, Characterization, Antioxidant Activity and Conformational Study of 4-Hydroxychalcone

open access: yesOrbital: The Electronic Journal of Chemistry, 2021
The objective of this work was to develop a synthesis, characterization, and conformational study of 4-hydroxychalcone. The chalcone was obtained using Claisen-Schmidt reaction. The product was characterized by IR and NMR spectroscopy.
André Luis Kerek   +2 more
doaj   +3 more sources

(E)-3-(4-Bromophenyl)-1-(3,4-dichlorophenyl)prop-2-en-1-one

open access: yesActa Crystallographica Section E, 2009
The molecule of the title compound, C15H9BrCl2O, is shown to be the E isomer, with the 3,4-dichlorobenzoyl and p-bromophenyl substituents in trans positions with respect to the chalcone olefin bond.
Rajni Kant   +4 more
doaj   +1 more source

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