Tong-Shuang Li
Hebei University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Tong-Shuang Li.
Synthetic Communications | 1998
Zhan-Hui Zhang; Tong-Shuang Li; Feng Yang; Cheng-Guang Fu
Abstract An easy preparation of trimethylsilyl ethers of alcohols and phenols with 1,1,1,3,3,3-hexamethyldisilazane(HMDS) catalysed by montmorillonite K-10 at room temperature has been carried out in excellent yields. Desilyation of trimethylsilyl ethers is catalysed by K-10 in methanol at ambient temperature in high yields.
Synthetic Communications | 1997
Tong-Shou Jin; Yan-Ran Ma; Zhan-Hui Zhang; Tong-Shuang Li
Abstract A rapid, efficient and high yield method for the deprotection of 1,1-diacetates is described which occurs under catalysis of expansive graphite in refluxing dichloromethane or benzene.
Synthetic Communications | 1998
Tong-Shuang Li; Zhan-Hui Zhang; Yong-Jian Gao
Abstract Aldehydes can be converted to acylals by treatment with acetic anhydride in the presence of Fe3+-montmorillonite in excellent yield at room temperature.
Synthetic Communications | 1997
Tong-Shou Jin; Gui-Ying Du; Zhan-Hui Zhang; Tong-Shuang Li
Abstract An easy preparation of 1,1-diacetates from aldehydes has been carried out in excellent yield under catalysis of expansive graphite at room temperature.
Synthetic Communications | 1997
Zhan-Hui Zhang; Feng Yang; Tong-Shuang Li; Cheng-Guang Fu
Abstract Triarylmethanes are synthesized in good to excellent yield via Baeyer condensation of aromatic aldehydes with N,N-dimethylaniline catalysed by montmorillonite K 10 at 100°C in the absence of solvent.
Synthetic Communications | 1998
Tong-Shou Jin; Tong-Shuang Li; Yong-Tao Gao
Abstract An easy preparation of methoxymethyl ethers of primary and secondary alcohols with dimethoxymethane has been carried out in excellent yield under catalysis of expansive graphite.
Synthetic Communications | 1996
Tong-Shuang Li; Huizhang Li; Juanli Guo; Tong-Shou Jin
Abstract In the presence of montmorillonite K 10, 5(6)-unsaturated sterols (1) were heated at refluxing temperature in dichloromethane to provide 5(6)/5′(6′)-unsaturated 3β,3′β-disteryl ethers (4) in 69–73% yield. The mechanism of the reaction was discussed.
Synthetic Communications | 1997
Tong-Shuang Li; Sheng-Hui Li
Abstract An easy cleavage of acetals has been carried out in excellent yield under catalysis of montmorillonite K 10 in refluxing wet acetone.
Synthetic Communications | 1996
Lijun Liu; Fajun Nan; Zhaoming Xiong; Tong-Shuang Li; Yulin Li
Abstract 9-Acetoxy-eudesma-4, 11-dien-3-ones (4a, 4b) and 9-acetoxy-14-noreudesma-4, 11-dien-3-ones (5a, 5b) were treated with DDQ in dioxane to yield normal 1,2-dehydro-products, whereas 14-noreudesma-4, 11-dien-3, 9-diones (2a, 2b) afforded a rearranged aromatic product, 1-hydroxy-15-noreudesma-1, 3, 5 (10), 11-tetraen-9-one(3). No reaction was observed by treatment of eudesma-4, 11-dien-3, 9-diones (1a, 1b) with DDQ under the same conditions. The effect of 10-methyl configuration on this reaction is also discussed.
Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry | 1998
Tong-Shou Jin; Gui-Ying Du; Tong-Shuang Li