7426-81-5Relevant articles and documents
NHC-CDI Betaine Adducts and Their Cationic Derivatives as Catalyst Precursors for Dichloromethane Valorization
Sánchez-Roa, David,Mosquera, Marta E. G.,Cámpora, Juan
, p. 16725 - 16735 (2021/11/18)
Zwitterionic adducts of N-heterocyclic carbene and carbodiimide (NHC-CDI) are an emerging class of organic compounds with promising properties for applications in various fields. Herein, we report the use of the ICyCDI(p-Tol) betaine adduct (1a) and its cationic derivatives2aand3aas catalyst precursors for the dichloromethane valorization via transformation into high added value products CH2Z2(Z = OR, SR or NR2). This process implies selective chloride substitution of dichloromethane by a range of nucleophiles Na+Z-(preformed or generatedin situfrom HZ and an inorganic base) to yield formaldehyde-derived acetals, dithioacetals, or aminals with full selectivity. The reactions are conducted in a multigram-scale under very mild conditions, using dichloromethane both as a reagent and solvent, and very low catalyst loading (0.01 mol %). The CH2Z2derivatives were isolated in quantitative yields after filtration and evaporation, which facilitates recycling the dichloromethane excess. Mechanistic studies for the synthesis of methylal CH2(OMe)2rule out organocatalysis as being responsible for the CH2transfer, and a phase-transfer catalysis mechanism is proposed instead. Furthermore, we observed that1aand2areact with NaOMe to form unusual isoureate ethers, which are the actual phase-transfer catalysts, with a strong preference for sodium over other alkali metal nucleophiles.
Synthesis and antimicrobial evaluation of 6-azauracil non-nucleosides
El-Brollosy, Nasser R.
scheme or table, p. 1483 - 1490 (2009/12/26)
The present study describes synthesis and antimicrobial evaluation of a series of novel 6-azauracil non-nucleosides. Reaction of silylated 6-azauracils with the appropriate chloroethers gave the corresponding non-nucleosides. 1-(Allyloxymethy)-6-azauracils and non-nucleosides bearing indanyl, cyclohexenyl, and cyclohexyl moieties were obtained via silylation of 6-azauracils followed by treatment with the appropriate acetals. Selected compounds were tested for their in vitro antimicrobial activity against a panel of standard strains of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Four compounds showed marked inhibitory activity particularly against the tested Gram-positive bacteria.
A novel synthesis of diallyloxymethanes
Kulkarni, G. Mukund,Davawala, Saryu I.,Doke, Aniruddha K.,Doke, Ajit V.
, p. 2121 - 2123 (2007/10/03)
Allylic alcohols on heating with sodium hydride and dihalomethanes furnish corresponding diallyloxymethanes in good yields.
Synthesis of novel N-1 (allyloxymethyl) analogues of 6-benzyl-1-(ethoxymethyl)-5-isopropyluracil (MKC-442, emivirine) with improved activity against HIV-1 and its mutants
El-Brollosy, Nasser R.,J?rgensen, Per T.,Dahan, Berit,Boel, Anne Marie,Pedersen, Erik B.,Nielsen, Claus
, p. 5721 - 5726 (2007/10/03)
This paper reports the synthesis and the antiviral activities of a series of 6-arylmethyl-1-(allyloxymethyl)-5-alkyluracil derivatives, which can be viewed as analogues of the anti-HIV-1 drug emivirine (formerly MKC-442) from which they differ in the repl
QUATERNARY AMMONIUM SALTS IN ALKYLATION REACTIONS (SYNTHESIS OF FORMALDEHYDE ACETALS).
Nazaretyan,Torosyan,Babayan
, p. 2396 - 2400 (2007/10/02)
The influence of the nature of the catalyst on the reaction yields was studied in the synthesis of formaldehyde bis( beta -methoxyethyl) and dibenzyl acetals. The acetal yields were not greatly influenced by the nature of the catalyst. The synthesis was also effected in presence of polymeric ammonium salts. In comparison with earlier results, the polymeric salts in this case were more effective than their monomeric analogs.
