Synthesis of polyfunctional triethoxysilanes by ‘click silylation’
摘要:
The copper-catalyzed 'click silylation' has been exploited for the chemical modification of gamma-azidopropyltriethoxysilane (AzPTES) with a wide range of terminal alkynes (la-lv) in a one-pot operation. The novel 1,2,3-triazole-triethoxysilane derivatives (2a-2v) were synthesized by this procedure and comprehensively characterized by IR spectra, H-1 and C-13 NMR, and HRMS studies. (C) 2013 Elsevier Ltd. All rights reserved.
A single step reaction for the synthesis of novel 1,2,3-triazole based silatranes (TBS)-scaffolds (2a–2o) usingpolyfunctionalised organotriethoxysilanes (1a–1l) as precursors is described. The synthesized silatranes are the first compounds of this type and hydrolytically more stable than their open chain analogues. The structures of 2a–2o were characterized by IR, NMR (1H and 13C) and mass spectroscopy
Synthesis of polyfunctional triethoxysilanes by ‘click silylation’
作者:Gurjaspreet Singh、Satinderpal Singh Mangat、Jandeep Singh、Aanchal Arora、Ramesh K. Sharma
DOI:10.1016/j.tetlet.2013.12.037
日期:2014.1
The copper-catalyzed 'click silylation' has been exploited for the chemical modification of gamma-azidopropyltriethoxysilane (AzPTES) with a wide range of terminal alkynes (la-lv) in a one-pot operation. The novel 1,2,3-triazole-triethoxysilane derivatives (2a-2v) were synthesized by this procedure and comprehensively characterized by IR spectra, H-1 and C-13 NMR, and HRMS studies. (C) 2013 Elsevier Ltd. All rights reserved.
Design and syntheses of novel fluorescent organosilicon-based chemosensors through click silylation: detection of biogenic amines