Results 21 to 30 of about 30,942 (194)

High chemoselectivity in the phenol synthesis

open access: yesBeilstein Journal of Organic Chemistry, 2011
Efforts to trap early intermediates of the gold-catalyzed phenol synthesis failed. Neither inter- nor intramolecularly offered vinyl groups, ketones or alcohols were able to intercept the gold carbenoid species. This indicates that the competing steps of
Matthias Rudolph   +3 more
doaj   +1 more source

Interaction between maleic acid and N-R-furfurylamines: crystal structure of 2-methyl-N-[(5-phenylfuran-2-yl)methyl]propan-2-aminium (2Z)-3-carboxyacrylate and N-[(5-iodofuran-2-yl)methyl]-2-methylpropan-2-aminium (2Z)-3-carboxyprop-2-enoate

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2017
The title molecular salts, C15H20NO+·C4H3O4−, (I), and C9H15INO+·C4H3O4−, (II), have very similar molecular geometries for both cation and anion. The anions of both (I) and (II) are practically planar (r.m.s. deviations = 0.062 and 0.072 Å, respectively)
Elisaveta A. Kvyatkovskaya   +5 more
doaj   +1 more source

QSTR Models in Dioxins and Dioxin-like Compounds Provide Insights into Gene Expression Dysregulation

open access: yesToxics
Polychlorinated dibenzo-p-dioxins and polychlorinated dibenzo-p-furans (PCDD/Fs) are a group of organic chemicals containing three-ring structures that can be substituted with one to eight chlorine atoms, leading to 75 dioxin and 135 furan congeners.
Elisa G. Eleazar   +4 more
doaj   +1 more source

Gold(I)-catalyzed formation of furans by a Claisen-type rearrangement of ynenyl allyl ethers

open access: yesBeilstein Journal of Organic Chemistry, 2011
A series of ynenyl allyl ethers were rearranged into polysubstituted furans in the presence of a gold(I) catalyst. It is proposed that the transformation involves a Claisen-type rearrangement that allows the efficient creation of quaternary centers under
Florin M. Istrate, Fabien Gagosz
doaj   +1 more source

Recent Trends in the Production, Combustion and Modeling of Furan-Based Fuels

open access: yesEnergies, 2018
There is growing interest in the use of furans, a class of alternative fuels derived from biomass, as transportation fuels. This paper reviews recent progress in the characterization of its combustion properties.
Mazen A. Eldeeb, Benjamin Akih-Kumgeh
doaj   +1 more source

Widespread distribution of hmf genes in Proteobacteria reveals key enzymes for 5-hydroxymethylfurfural conversion

open access: yesComputational and Structural Biotechnology Journal, 2021
Furans represent a class of promising chemicals, since they constitute valuable intermediates in conversion of biomass into sustainable products intended to replace petroleum-derivatives.
Raúl A. Donoso   +2 more
doaj   +1 more source

Chemotaxis to Furan Compounds by Furan-Degrading Pseudomonas Strains [PDF]

open access: yesApplied and Environmental Microbiology, 2012
ABSTRACT Two Pseudomonas strains known to utilize furan derivatives were shown to respond chemotactically to furfural, 5-hydroxymethylfurfural, furfuryl alcohol, and 2-furoic acid. In addition, a LysR-family regulatory protein known to regulate furan metabolic genes was found to be involved in regulating ...
Nancy N, Nichols   +7 more
openaire   +3 more sources

Transition Metal-Free Synthesis of Halobenzo[b]furans from O-Aryl Carbamates via o-Lithiation Reactions

open access: yesMolecules, 2022
A straightforward and transition metal-free one-pot protocol to synthesize halobenzo[b]furans has been developed employing simple and easily available starting materials such as O-aryl carbamates and alkynylsulfones.
Claudia Feberero   +5 more
doaj   +1 more source

A Diels–Alder probe for discovery of natural products containing furan moieties

open access: yesBeilstein Journal of Organic Chemistry
Natural products (NPs) are fantastic sources of inspiration for novel pharmaceuticals, oftentimes showing unique bioactivity against interesting targets.
Alyssa S. Eggly   +5 more
doaj   +1 more source

Gold-Catalyzed Propargylic Substitution Followed by Cycloisomerization in Ionic Liquid: Environmentally Friendly Synthesis of Polysubstituted Furans from Propargylic Alcohols and 1,3-Dicarbonyl Compounds

open access: yesMolecules
Gold-catalyzed propargylic substitution of propargylic alcohols 1 with 1,3-dicarbonyl compounds 2 followed by cycloisomerization in ionic liquid enables the environmentally friendly synthesis of polysubstituted furans 3 in good-to-high yields.
Hitomi Chiaki   +2 more
doaj   +1 more source

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