The use of Bronsted acid ionic liquid (BAIL) as a catalyst for the activation of unreactive and unprotected glycosyl donors has been demonstrated for the first time in aqueous solution. (c) 2013 Elsevier Ltd. All rights reserved.
Preparation of 5-Substituted 1<i>H</i>-Tetrazoles Catalyzed by Scandium Triflate in Water
作者:Adiel Coca、Evan Turek、Liana Feinn
DOI:10.1080/00397911.2014.957775
日期:2015.1.17
Abstract Several 5-substituted1H-tetrazoles were prepared in water or isopropanol/water mixtures using microwave heating. Good yields were obtained for the [2 + 3] cycloaddition of sodium azide with aryl nitriles, aliphatic nitriles, and vinyl nitriles when catalyzed by scandium triflate. The reactions were typically heated for 1 h at 160 °C in a 3:1 isopropanol/water mixture to obtain the best yields
Microwave Synthesis of 5-Substituted 1<i>H</i>-Tetrazoles Catalyzed by Bismuth Chloride in Water
作者:Adiel Coca、Liana Feinn、Joshua Dudley
DOI:10.1080/00397911.2014.989451
日期:2015.4.18
Abstract Bismuth chloride was used to catalyze the [2 + 3] cycloaddition between sodium azide with aryl nitriles, aliphatic nitriles, and vinyl nitriles. A number of 5-substituted1H-tetrazoles were synthesized in water or isopropanol/water mixtures using microwave heating. Good yields were obtained for these reactions when heated for 1 h at 120–160 °C in a 3:1 isopropanol/water mixture. A few of the
[EN] FUSED PIPERIDINES AS IP RECEPTOR AGONISTS FOR THE TREATMENT OF PULMONARY ARTERIAL HYPERTENSION (PAH) AND RELATED DISORDERS<br/>[FR] PIPÉRIDINES CONDENSÉES UTILISÉES COMME AGONISTES DU RÉCEPTEUR IP POUR LE TRAITEMENT DE L'HYPERTENSION ARTÉRIELLE PULMONAIRE (HTAP) ET DE TROUBLES ASSOCIÉS
申请人:NOVARTIS AG
公开号:WO2013105063A1
公开(公告)日:2013-07-18
The present invention provides heterocyclic derivatives which activate the IP receptor, processes for preparing them, pharmaceutical compositions comprising said derivatives and uses thereof. Activating the IP receptor signaling pathway is useful to treat many forms of PAH, pulmonary fibrosis and exert beneficial effects in fibrotic conditions of various organs in animal models and in patients. Formula (I):
Preparation of 5-Substituted 1<i>H</i>-Tetrazoles from Nitriles in Water
作者:Zachary P. Demko、K. Barry Sharpless
DOI:10.1021/jo010635w
日期:2001.11.1
The addition of sodium azide to nitriles to give 1H-tetrazoles is shown to proceed readily in water with zinc salts as catalysts. The scope of the reaction is quite broad; a variety of aromatic nitriles, activated and unactivated alkyl nitriles, substituted vinyl nitriles, thiocyanates, and cyanamides have all been shown to be viable substrates for this reaction.
TETRAZOLE SILANE COMPOUND, METHOD FOR SYNTHESIZING SAID COMPOUND AND USE THEREOF
申请人:SHIKOKU CHEMICALS CORPORATION
公开号:US20200223875A1
公开(公告)日:2020-07-16
The objectives of the present invention are: to provide a novel tetrazole silane compound, a method for synthesizing the same, and a silane coupling agent containing the tetrazole silane compound as a component; and to provide a surface treatment solution using the tetrazole silane compound, a method for surface treatment, and a method for adhering two different materials. The tetrazole silane compound according to the present invention is a compound represented by chemical formula (I). (In formula (I), X, R, and n are respectively the same as defined in the specification.)