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Nucleophile- or light-induced synthesis of 3-substituted phthalides from 2-formylarylketones
(American Chemical Society, 2012-05)
The surprisingly facile conversion (isomerization) of 2-formyl-arylketones into 3-substituted phthalides, as observed for the marine natural product pestalone and its per-O-methylated derivative, was investigated using a ...
Antiproliferative effect of Baylis-Hillman adducts and a new phthalide derivative on human tumor cell lines
(Elsevier France-editions Scientifiques Medicales ElsevierParisFrança, 2006)
Expeditious synthesis of 3,4-dihydroisocoumarins and phthalides using the Heck-Matsuda reaction
(Pergamon-elsevier Science LtdOxfordInglaterra, 2011)
A new phthalide derivative from Peperomia nivalis
(Taylor and Francis, 2016)
One new phthalide (1) was isolated from aerial parts of Peperomia nivalis, along with known compounds (2 and 3), reported in this species for the first time. The structure of the new compound was characterised on the basis ...
Toxicity and sublethal effects of phthalides analogs to Rhyzopertha dominica
(Chemistry e Biodiversity, 2019)
Synthesis, characterization and phytotoxic activity of hydroxylated isobenzofuran-1(3H)-ones
(Elsevier BVAmsterdam, 2014-03)
Two hydroxylated isobenzofuranones 3 and 4 were synthesized from benzoic acids. The compounds were fully characterized by IR, NMR (1H and 13C), HRMS, and X-ray crystallography. Compounds 3 and 4 crystallized in the space ...
Computation and structural elucidation of compounds formed via epoxide alcoholysis
(Magnetic Resonance in Chemistry, 2019)
Characterization of novel isobenzofuranones by DFT calculations and 2D NMR analysis
(Magnetic Resonance in Chemistry, 2018)
[2 + 2 + 2]-Cycloaddition Reactions Using Immobilized Alkynes. A Proof of Concept for an Integral Use of the Outcoming Products in Solid-Phase Synthetic Methodologies
(American Chemical Society, 2018-09)
The transition-metal-catalyzed [2 + 2 + 2]-cycloaddition of alkynes has become a powerful atom-economical strategy for aromatic ring construction. Unfortunately, the control of the stereo-, regio-, and chemoselectivity of ...