Results 61 to 70 of about 42,977 (261)

1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives

open access: yesMolecules, 2016
We provide a comprehensive account of the 1,3-dipolar cycloaddition reactions of azomethine ylides with carbonyl dipolarophiles. Many different azomethine ylides have been studied, including stabilized and non-stabilized ylides.
A. G. Meyer, J. H. Ryan
semanticscholar   +1 more source

Reactivity mapping: electrochemical gradients for monitoring reactivity at surfaces in space and time [PDF]

open access: yes, 2013
Studying and controlling reactions at surfaces is of great fundamental and applied interest in, among others, biology, electronics and catalysis.
Chen, P.   +3 more
core   +2 more sources

Synthesis of Novel Spiro-Isoxazolidine Derivatives of 9α-Hydroxyparthenolide

open access: yesMolbank
The 1,3-dipolar cycloaddition reaction was applied to 9α-hydroxyparthenolide, an important sesquiterpene component of Anvillea radiata that was extracted directly from plant material collected in Morocco.
Mohamed Zaki   +2 more
doaj   +1 more source

Dimerization of propargyl and homopropargyl 6-azido-6-deoxy-glycosides upon 1,3-dipolar cycloaddition

open access: yesBeilstein Journal of Organic Chemistry, 2008
Copper-catalyzed, thermal or microwave promoted 1,3-dipolar cycloaddition (Click Reaction) of 2-propynyl and 3-butynyl 2,3,4-tri-O-acetyl-6-azido-6-deoxy-glycopyranosides in the D-gluco, D-galacto and D-manno series afford the corresponding dimeric ...
Nikolas Pietrzik   +2 more
doaj   +1 more source

Influence of activated carbons on the kinetics and mechanisms of aromatic molecules ozonation [PDF]

open access: yes, 2010
Companies have been looking for new methods for treating toxic or refractory wastewaters; which can mainly be used prior to or after or in connexion with biological treatment processes.This paper compares conventional ozone oxidation with activatedcarbon
Debellefontaine, Hubert   +4 more
core   +2 more sources

Synthesis of New bis 1- and 5-Substituted 1H-Tetrazoles via Huisgen-Type 1,3-Dipolar Cycloadditions

open access: yesProceedings, 2019
The synthesis and characterization of one symmetrical bis-1-substituted-1H-tetrazole (69%) via a Huisgen-type 1,3-dipolar cycloaddition, as well as, one symmetrical aza-linked bis-5-substituted-1H-tetrazole (57%) via a classic Huisgen 1,3-dipolar ...
Roberto E. Blanco-Carapia   +8 more
doaj   +1 more source

Advancing from MOFs and COFs to Functional Macroscopic Porous Constructs

open access: yesAdvanced Materials, EarlyView.
This review study investigates the recent progress and methodologies for manufacturing metal–organic framework (MOF) or covalent–organic framework (COF)‐based 3D structured macroscopic porous constructs with high structural integrity, providing the possibility to control their porosity across dimensions.
Seyyed Alireza Hashemi   +8 more
wiley   +1 more source

1,3-Dipolar cycloadditions of fluorinated nitrones with thioketones [PDF]

open access: yesJournal of Fluorine Chemistry, 2014
AbstractReadily available fluorinated nitrones (IV) and (XIV) are used in 1,3‐dipolar cycloadditions with thioketones affording 1,4,2 oxathiazolidines in a regioselective manner.
Mlostoń, Grzegorz   +5 more
openaire   +3 more sources

Inverse electron-demand 1,3-dipolar cycloaddition of nitrile oxide with common nitriles leading to 3-functionalized 1,2,4-oxadiazoles [PDF]

open access: yes, 2011
A carbamoyl-substituted nitrile oxide was generated upon treatment of easily available 2-methyl-4-nitro-3-isoxazolin-5(2H)-one with THF (not dried); the reaction proceeded efficiently even in the absence of any special reagents and reaction conditions ...
1020   +15 more
core   +1 more source

Ultrasound-promoted synthesis of novel fused heterocycles by criss-cross cycloaddition

open access: yesJournal of Saudi Chemical Society, 2016
This work reports a novel and highly efficient methodology for the synthesis of perhydrotriazolotriazoledithions from two successive 1,3-dipolar cycloaddition under ultrasound irradiation.
Javad Safari   +2 more
doaj   +1 more source

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