相关期刊:《Journal of Wuhan University of Technology(Materials Science)》《Journal of Chemistry and Chemical Engineering》《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》《Chinese Journal of Chemistry》更多>>
supported by the National Natural Science Foundation of China(Nos.82130103,82151525 and 81903465);the Central Plains Scholars and Scientists Studio Fund(2018002);the Natural Science Foundation of Henan Province(No.212300410051);the Science and Technology Major Project of Henan Province(No.221100310300)。
Herein,we report the dynamic kinetic resolution asymmetric acylation ofγ-hydroxy-γ-perfluoroalkyl butenolides/phthalides catalyzed by amino acid-derived bifunctional organocatalysts,and a series of ketals were obtai...
A series of stable semi-ketals were obtained via the reactions of 3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)-2'-ketouridine 1 with primary alcohols. In the addition reaction,only a single diastereomer was observed. T...
3-Methoxy-, 3, 5-dimethoxy-, and 3-phenyl-4-hydroxyacetophenones suffered alkyl carbonyl C-C bond scission to yield 4-hydroxybenzoate esters and 4-isopropenylphenols under standard conditions of ethylene ketal formati...
The acetalization of a series of carbonyl compounds with ethanediolwas performed over two self-steaxned HY zeolle catalpsts' The acetal and ketaiproducts were obtained with high ytelds Espectw, the HY zeollte with hig...
The 1,3-dioxolanes, 1,3-dioxanes and open chain acetals or ketals are easily cleavaged by using sodium hydrogen selenide under basic conditions in high yields.
A new method for aromatization of Δ^(5(10))-steroidal C_3-dimethyl ketals with pyridinium hydrobromide perbromide (PHP.Py·HBr·Br_2) to aromatic A ring steroids in high yield (90-95%) is described.
When the mixture of CpTiCl_3-KI is used, many acetals and ketals, which are difficuitly deprotected with CpTiCl_3 alone, can be easily converted to the corresponding carbonyl compounds in high yield at 30℃ in Et_2O.
In our study on the chemistry of ZrCl_4-NaBH_4,we have found that aldehydes and ketones can be regenerated from acetals and ketals at 30℃ in Et_2O in high yield The reaction mechanism was discussed.