401515-97-7Relevant academic research and scientific papers
RAPAMYCIN ANALOG
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Paragraph 0095, (2018/09/08)
The present invention relates to a novel rapamycin analogue (e.g., of Formula I or Formula II), mixtures, methods for its production, and its use in cancer therapy (e.g., prevention and/or treatment).
Method for preparing formate-type compound
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Paragraph 0039; 0047; 0048, (2018/07/30)
The invention discloses a method for preparing a formate-type compound. The method comprises the following steps of: adopting an alcohol-type compound and 1,3-dihydroxyacetone as reaction raw materials, and under the existence of a composite catalyst and an oxidant, reacting for 2-48 hours in a reaction medium in a reactor at a reaction temperature of 25-100 DEG C so as to obtain the formate-typecompound. The method disclosed by the invention is simple, and is mild in reaction condition, and by the method, a target product can be obtained by low cost and high yield; the used catalyst has highcatalytic activity, and is easily separated from a reaction system to be repeatedly used; the whole process is environment-friendly, and the reaction raw material (1,3-dihydroxyacetone) is easily converted from a side product (glycerol) of biodiesel, so that the utilization of the glycerol is promoted.
Silica triflate as an efficient reagent for the chemoselective formylation of alcohols
Shirini, Farhad,Marjani, Katayoun,Nahzomi, Hossein Taherpour,Zolfigol, Mohammad Ali
, p. 1245 - 1251 (2008/02/05)
Silica triflate, as a new and stable silica-based reagent, is prepared by a reaction of silica gel with trifluoromethane sulfonyl chloride at room temperature. This reagent can be used for the efficient and selective formylation of alcohols in the presence of phenols in a relatively short reaction time and high yields under heterogeneous reaction conditions.
Formate as a CO surrogate for cascade processes: Rh-catalyzed cooperative decarbonylation and asymmetric Pauson-Khand-type cyclization reactions
Lee, Hang Wai,Chan, Albert S. C.,Kwong, Fuk Yee
, p. 2633 - 2635 (2008/02/08)
A rhodium-(S)-xyl-BINAP complex-catalyzed tandem formate decarbonylation and [2 + 2 + 1] carbonylative cyclization is described; this cooperative process utilizes formate as a condensed CO source, and the newly developed cascade protocol can be extended t
Investigations of the scope and mechanism of the tandem hydroesterification/lactonization reaction
Wang, Lijun,Floreancig, Paul E.
, p. 4207 - 4210 (2007/10/03)
(Chemical Equation Presented) Heating allylic and homoallylic alcohols and 2-pyridylmethyl formate in the presence of Ru3(CO)12 initiates a tandem sequence of hydroesterification and lactonization. Mechanistic studies suggest that regioselectivity and overall reaction efficiency are governed by the relative rates of reductive elimination and β-hydride elimination for the alkylruthenium intermediates.
A novel chelation-assisted hydroesterification of alkenes via ruthenium catalysis
Ko, Sangwon,Na, Youngim,Chang, Sukbok
, p. 750 - 751 (2007/10/03)
An efficient and catalytic protocol of hydroesterification of alkenes has been developed without a need for CO atmosphere. With the introduction of the 2-pyridyl moiety as a chelating group in formate, Ru3(CO)12-catalyzed activation of the formyl C-H bond of formate and subsequent addition of the intermediate to alkenes proceeded with almost complete suppression of decarbonylation. Stereoselectivity of the produced one-carbon elongated esters was good to excellent for the formation of the linear adduct depending on the bulkiness of the alkenes used. This procedure could be readily applied to a variety of olefins such as terminal, internal, cyclic, bicyclic, vinyl ether, and conjugated enone systems with high efficiency and selectivity. It was also amenable to a solvent-free condition. On the basis of the chelation-driven C-H bond activation of formate, a putative mechanism of the Ru-catalyzed hydroesterification of 2-pyridylmethyl formate has been proposed. Copyright
