نتایج جستجو برای: triethyl orthoesters

تعداد نتایج: 511  

2010
Ezzatollah Najafi Mostafa M. Amini Seik Weng Ng

The reaction between benzyl-triethyl-ammonium chloride and dimethyl-tin dichloride yields the title salt, [(C(6)H(5)CH(2))(C(2)H(5))(3)N](2)[SnCl(6)]. The Sn(IV) atom, located on a center of inversion, exists in an octa-hedral coordination environment. The cation links with the anion via weak C-H⋯Cl hydrogen bonding.

Journal: :Organic & biomolecular chemistry 2013
Honorine Lebraud Celine Cano Benoit Carbain Ian R Hardcastle Ross W Harrington Roger J Griffin Bernard T Golding

Purines protected at N-9 by p-methoxybenzyl are methylated or ethylated in 2,2,2-trifluoroethanol at N-7 by trimethyl- or triethyl-oxonium borofluorate, respectively. Subjecting the resulting cationic species to microwave irradiation releases an N(7)-methyl- or ethyl-purine. This one-pot procedure is an efficient regiospecific method applicable to diverse substrates.

2011
Brahim Boualy Mohamed Anoir Harrad Larbi El Firdoussi Mustapha Ait Ali Corrado Rizzoli

The title compound, C(11)H(16)Cl(4), was synthesized by the reaction of (1S)-β-pinene with triethyl-amine in the presence of ZnCl(2). The cyclo-hexene ring assumes a half-boat conformation. The crystal packing is governed only by van der Waals inter-actions. The structure, which has been refined in P2(1), presents a striking P2(1)/m pseudosymmetry.

2013
Shingo Ishikawa Tom D Sheppard Jarryl M D'Oyley Akio Kamimura William B Motherwell

Easy as 1,2,3: Reaction of methyl carbamate, triethyl orthoformate, and readily available alkenes provides a highly practical preparation of protected aminocyclopropanes. The reaction proceeds with preferential cis addition to alkenes, and cleavage of the methyl carbamate gives the free aminocyclopropanes as their HI salts.

2015
Sandrina Oliveira Dulce Belo Isabel Cordeiro Santos Sandra Rabaça Manuel Almeida

A dissymmetric TTF-type electron donor, cyanobenzene-ethylenedithio-tetrathiafulvalene (CNB-EDT-TTF), was obtained in high yield, by a cross-coupling reaction with triethyl phosphite between 2-thioxobenzo[d][1,3]dithiole-5-carbonitrile and 5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-one. This new donor was characterized namely by single crystal X-ray diffraction, cyclic voltammetry, NMR, UV-...

Journal: :Catalysts 2021

A protocol for the coupling of potassium xanthogenates with ?-(trifluoromethyl)styrenes in presence triethyl phosphite is reported. The reaction carried out under blue light irradiation organic photocatalyst 3DPAFIPN. proceeds via formation alkyl radicals from readily available xanthogenate salts oxidative desulfurization and cleavage carbon–oxygen bond assisted by phosphite.

Journal: :Journal of lipid research 1971
Y Eto K Suzuki

Chronic triethyl tin intoxication was induced in young adult rats by oral feeding of triethyl tin sulfate. Progressively severe brain edema developed during the 3-month experimental period. The yield of myelin from the brains of the experimental animals decreased to almost half normal per brain, but the isolated myelin appeared morphologically normal. The analysis of whole brain showed correspo...

Journal: :Bulletin of the Chemical Society of Japan 1977

2008
Masumi Itazaki Masahiro Kamitani Hiroshi Nakazawa

In the title complex, [Fe(C(5)H(5)){Sn(C(2)H(5))(3)}(C(5)H(5)N)(CO)], the Fe atom is coordinated by carbonyl, pyridine, triethyl-stannyl and cyclo-penta-dienyl ligands in a typical three-legged piano-stool configuration. The Fe-Sn and Fe-N bond distances are 2.5455 (13) and 1.984 (6) Å, respectively.

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