Results 21 to 30 of about 62,486 (246)

Synthesis of α-Heterosubstituted Ketones Through Sulfur Mediated Difunctionalization of Internal Alkynes [PDF]

open access: yes, 2019
Synthesis of α-heterosubstituted ketones was achieved through sulfur mediated difunctionalization of internal alkynes in one-pot. The reaction design involves: phenyl substituted internal alkyne attacking the triflic anhydride activated diphenyl ...
Hongguang, Du   +3 more
core   +1 more source

Alkynes as Synthetic Equivalents of Ketones and Aldehydes: A Hidden Entry into Carbonyl Chemistry

open access: yesMolecules, 2019
The high energy packed in alkyne functional group makes alkyne reactions highly thermodynamically favorable and generally irreversible. Furthermore, the presence of two orthogonal π-bonds that can be manipulated separately enables flexible synthetic ...
Igor V. Alabugin   +4 more
doaj   +1 more source

Occupational exposure to ketones [PDF]

open access: yes
"Recommended standards and criteria to prevent hazardous workplace exposure to ketones are presented. Information on the biological effects of ketones is included along with data on environmental sampling, analysis, and control.

core   +1 more source

Generating structural diversity in \(\alpha\)[alpha],\(\alpha\)[alpha]-difluoromethyl ketones [PDF]

open access: yes, 2003
This thesis describes attempts to use palladium-catalysed cross-coupling methodology in the synthesis of \(\alpha\),\(\alpha\)-difluoroketones contained within a diverse array of molecular motifs.
Fullbrook, Jeremy Jon
core   +7 more sources

Mechanically induced oxidation of alcohols to aldehydes and ketones in ambient air: Revisiting TEMPO-assisted oxidations

open access: yesBeilstein Journal of Organic Chemistry, 2017
The present work addresses the development of an eco-friendly and cost-efficient protocol for the oxidation of primary and secondary alcohols to the corresponding aldehydes and ketones by mechanical processing under air. Ball milling was shown to promote
Andrea Porcheddu   +4 more
doaj   +1 more source

Enantioselective Oxidative Multi-Functionalization of Terminal Alkynes with Nitrones and Alcohols for Expeditious Assembly of Chiral Alkoxy--amino-ketones

open access: yes, 2021
Catalytic oxidative functionalization of alkynes has emerged as an effective method in synthetic chemistry in recent decades. However, enantioselective transformations via metal carbene intermediates are quite rare due to the lack of robust chiral ...
Wenhao Hu   +11 more
core   +1 more source

Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-induced cyclizations

open access: yesBeilstein Journal of Organic Chemistry, 2010
A series of γ-oxo esters suitably substituted with various styrene subunits was subjected to samarium diiodide-induced 8-endo-trig cyclizations. Efficacy, regioselectivity and stereoselectivity of these reactions via samarium ketyls strongly depend on ...
Jakub Saadi   +2 more
doaj   +1 more source

Naturally occurring long-chain β-hydroxyketones

open access: yesJournal of Lipid Research, 1971
A fraction comprising about 0.7% of the extractable surface lipids of cabbage (Brassica oleracea) leaves was isolated and identified as a mixture of isomeric βhydroxyketones consisting mainly of 14-keto-16-hydroxynonacosane and 15-keto-13 ...
HARALD H.O. SCHMID, PATRICIA C. BANDI
doaj   +1 more source

Comparison of the structure and thermal properties of a poly(aryl ether ketone ether ketone naphthyl ketone) with those of poly(aryl ether ketone ether ketone ketone)

open access: yese-Polymers, 2007
Abstract Poly(oxy-1,4-phenylene carbonyl-1,4-phenylene oxy-1,4-phenylene carbonyl-2,6-naphthalene carbonyl-1,4-phenylene) or 2,6-PEKEKNK is a polymer of the poly(aryl ether ketone) family differing from PEKEKK by the presence of a naphthyl group linked at positions 2 and 6 to the two ketone groups.
Dosière, Marcel   +3 more
openaire   +1 more source

Simple synthesis of pyrrolo[3,2-e]indole-1-carbonitriles

open access: yesBeilstein Journal of Organic Chemistry, 2013
Alkylation of 5-nitroindol-4-ylacetonitriles with ethyl chloroacetate, α-halomethyl ketones, and chloroacetonitrile followed by a treatment of the products with chlorotrimethylsilane in the presence of DBU gives 1-cyanopyrrolo[3,2-e]indoles substituted ...
Adam Trawczyński   +3 more
doaj   +1 more source

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