نتایج جستجو برای: acetal formation

تعداد نتایج: 527971  

Journal: :Journal of Photopolymer Science and Technology 2002

Journal: :Beilstein Journal of Organic Chemistry 2013

Journal: :Journal of Photopolymer Science and Technology 1999

Journal: :The Journal of organic chemistry 2006
Gerry A Griffith Ian H Hillier Jonathan M Percy Ricard Roig Mark A Vincent

A simple enol acetal underwent rapid cleavage in acidic solution to generate a difluorinated enol, which was sufficiently long-lived to be characterized by 2D NMR in a protic solvent at ambient temperature. Density functional theory calculations on a model reaction suggest that there are significant differences in protonation transition state timing between the fluorinated and nonfluorinated en...

Journal: :Chemical science 2015
Cody Ross Pitts Michelle Sheanne Bloom Desta Doro Bume Qinze Arthur Zhang Thomas Lectka

Expanding the repertoire of controlled radical fluorination techniques, we present a photosensitized unstrained C-C bond activation/directed monofluorination method using Selectfluor and 9-fluorenone. The reaction is amenable to the opening of multiple 1-acetal-2-aryl substituted rings to yield ω-fluoro carboxylic acids, esters, alcohols, and ketones with relative ease. Initial mechanistic insi...

Journal: :Organic letters 2010
Richard W Heidebrecht Brian Gulledge Stephen F Martin

The synthesis of a functionalized, tetracyclic core of N-methylwelwitindolinone C isothiocyanate is reported. The approach features a convergent coupling between an indole iminium ion and a highly functionalized vinylogous silyl ketene acetal followed by an intramolecular palladium-catalyzed cyclization that proceeds via an enolate arylation.

Journal: :Chemical communications 2015
Marc-André Courtemanche Alexander P Pulis Étienne Rochette Marc-André Légaré Douglas W Stephan Frédéric-Georges Fontaine

The FLP species 1-BR2-2-NMe2-C6H4 (R = 2,4,6-Me3C6H2, 2,4,5-Me3C6H2) reacts with H2 in sequential hydrogen activation and protodeborylation reactions to give (1-BH2-2-NMe2-C6H4)2. While reacts with H2/CO2 to give formyl, acetal and methoxy-derivatives, reacts with H2/CO2 to give C6H4(NMe2)(B(2,4,5-Me3C6H2)O)2CH2. The mechanism of CO2 reduction is considered.

Journal: :Bioscience, biotechnology, and biochemistry 2010
Yue Qi Ye Hiroyuki Koshino Jun-ichi Onose Kunie Yoshikawa Naoki Abe Shunya Takahashi

A powerful inhibitor of TNF-alpha production, vialinin A, was synthesized from sesamol through a series of reactions involving double Suzuki-Miyaura coupling, 2,3-dichloro-5,6-dicyano-1,4-benzoquino (DDQ) mediated de-methoxymethylation and oxidative removal of methylene acetal by lead tetraacetate. The synthetic method also made it possible to prepare a related compound, terrestrin B.

2008
Li Wang Wei You Wei Huang Jue-Chao Jiang Cheng Yao

In the title compound, C(17)H(16)O(2), a dimethyl acetal of 9-anthraldehyde, the anthracene skeleton is planar and the two meth-oxy groups attached to the C atom at position 9 of the aromatic ring system are located above and below the ring system.

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