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1.
The 2,2,2-trichloroethoxycarbonyl (Troc) protecting group was efficiently removed from Troc-protected aliphatic and aromatic amines and also some Troc, Tos- and Troc, Ac-protected amines using activated mischmetal (MM). All reactions were performed by refluxing in dry tetrahydrofuran under an argon atmosphere and gave moderate to excellent yields. Several new compounds were synthesized, and new data about reactivity of Troc group were obtained. 相似文献
2.
Zilong Tang Zhonghua Zhu Lin Yan Shuhong Chang Hanwen Liu 《Journal of heterocyclic chemistry》2013,50(5):1116-1120
A series of novel substituted 3,4‐dihydro‐2H‐1,3‐benzoxazines were prepared in moderate to good yields by aza‐acetalizations of aromatic aldehydes with 2‐(N‐substituted aminomethyl)phenols in the presence of chlorotrimethylsilane or SnCl4. It was found that chlorotrimethylsilane was more effective for the reaction, especially for the reaction of fluorobenzaldehyde, and thereby, an efficient method for the preparation of 3,4‐dihydro‐2H‐1,3‐benzoxazines was developed. The structures of the compounds were determined by FT‐IR, 1H NMR, 13C NMR, MS, and elemental analysis. 相似文献
3.
Volodymyr Kysil Sergey Tkachenko Caroline Williams Marina Churakova 《Tetrahedron letters》2007,48(36):6239-6244
New trimethylchlorosilane (TMSCl) promoted multicomponent reaction (MCR) of ethylenediamine(s), diverse carbonyl compounds, and isocyanides is proposed for the synthesis of a variety of highly substituted 3,4,5,6-tetrahydropyrazin-2-amines including corresponding spirocyclic compounds. 相似文献
4.
Shengjun Huang Jun Liao Qingjie Zhao Xiaoyun Chai Baogang Wang Shichong Yu 《Journal of carbohydrate chemistry》2013,32(2):158-168
TMSCl was shown to be an efficient reagent for selective deprotection of the anomeric position protected as N,O-dimethylhydroxylamine glycoside. This deprotection condition was proved to be compatible with a number of protecting groups, such as the TBDPS, acetyl, benzyl, benzylidene, and benzoyl groups. 相似文献
5.
Synthesis of Pharmacologically Active Bis(indolyl) and Tris(indolyl) Derivatives Using Chlorotrimethylsilane 下载免费PDF全文
Nongthombam G. Singh Chingrishon Kathing Jims W. S. Rani Rishan L. Nongkhlaw 《中国化学会会志》2014,61(4):442-446
Chlorotrimethylsilane is found to be a comparatively fast and efficient catalyst for carrying out electrophilic substitution reactions of indoles with various aldehydes/ketones/triethylorthoformate, yielding excellent amount of bis(indolyl)methanes/tris(indolyl)methanes. The merits of this protocol are avoidance of any external energy source, minimal reaction time, simple and easy procedure and high yield under solvent free room temperature condition. The versatility of this method has been tested with various aldehydes/ketones and received satisfactory results. 相似文献
6.
Preparation of Nano Silica Supported Sodium Hydrogen Sulfate: As an Efficient Catalyst for the Trimethyl,Triethyl and t‐Butyldimethyl Silylations of Aliphatic and Aromatic Alcohols in Solution and under Solvent‐free Conditions 下载免费PDF全文
Nano silica supported sodium hydrogen sulfate has been prepared by mixing NaHSO4 with activated Nano silicagel. We wish to report a new method for the synthesis of trimethyl (TMS), triethyl (TES) and t‐butyldimethyl silyl (TBS) ethers from benzylic, allylic, propargylic alcohols, phenols, naphtholes and some of phenolic drugs in the solution and under solvent‐free conditions. 相似文献
7.
General and practical method for the synthesis of silyl ethers in the presence of zinc powder under mild conditions has been described. 相似文献
8.
Functionalized cyclopentenes could be prepared through Sm/TMSCl/t-BuOH mediated hy-drodimerization cyclization of gem-diactivated alkene in one-pot at mom temperature. The trans- or trans, transform isomer is in the majority and the major product was isolated from its stereoisomers through the fractional crystallization method. 相似文献
9.
Treatment of a mixture of alkyl aldehydes (1) with acid chlorides (2) in the presence of zinc metal powder and a catalytic amount of chlorotrimethylsilane (TMSCl) in dichloromethane brought about highly facile and effective coupling to give selectively the corresponding α-haloacylation and gem-bisacylation products, α-haloalkyl carboxylates and 1,1-dicarboxylates (acylals), in good to excellent yields. 相似文献
10.