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Faeze Nourmandipour,Reihane Emadi,Peyman Salehi et al. Faeze Nourmandipour et al.
This compound, as starting material for the click reaction underwent 1,3-dipolar cycloaddition reaction with different azides to produce the target 1,2,3-triazole tethered derivatives of morphine. The anti-nociceptive properties of the products were evaluated by tail flick test.
Kana M Sureshan,Divina Xavier,Sourav Pathak et al. Kana M Sureshan et al.
Upon heating at a temperature above 70 οC, each enantiomorphic crystal underwent a regiospecific and stereospecific topochemical ene-azide cycloaddition reaction in a single-crystal-to-single-crystal fashion to give a triazoline-linked homochiral helical polymer.
Yao Chen,Zhiqiang Wei,Haixia Song et al. Yao Chen et al.
A copper-catalyzed decarboxylative cycloaddition of (perfluoro-tert-butyl)propiolic acid (PFtPA) with azides under mild conditions was developed, enabling the facile synthesis of perfluoro-tert-butyl (PFtB) triazoles....The strong electron-withdrawing nature of the PFtB group facilitates efficient decarboxylative cycloaddition at 30 °C using catalytic copper acetate, avoiding the requirement of traditional harsh conditions.
Xin-Xin Liu,Jia-Jia Ma,Guo Li et al. Xin-Xin Liu et al.
The Cu(I)-photocatalyzed cycloaddition reaction has become an important way to construct four-membered ring products. A recent experiment reported the photocycloaddition of norbornenes (nb) and cyclohexenes (ch) catalyzed by CuOTf. However, the atomic level details remain lacking.
Kai Hu,Haijian Wu,Manman Sun et al. Kai Hu et al.
A HFIP-promoted formal [2π+2σ] cycloaddition of bicyclo[1.1.0]butanes with α-cyano chalcones has been reported, in which HFIP acts as the hydrogen-bond activator of both substrates, the stabilizer of carbocations and a co-solvent.
Fei Liu,Tongdao Wang Fei Liu
The [3 + 2] cycloaddition of Lewis acidic alkenylboranes with aldehydes is described, providing a high-yielding and stereoselective approach for the synthesis of five-membered boron-containing heterocycles. Notably, alkenylboranes are used as three-atom B-C═C building blocks.
Elijah C Gonzalez,Isabel M de la Torre Roehl,Brian M Stoltz Elijah C Gonzalez
Our de novo approach provided expedient access to the tetracyclic core of (+)-daphnepapytone A through an intramolecular allenyl thermal [2 + 2] cycloaddition and a Pauson-Khand reaction with a labile cyclobutane.
Daniel González-Pinardo,Rajendra S Ghadwal,Israel Fernandez Daniel González-Pinardo
Additionally, the key factors governing dihydrogen activation and cycloaddition with acetylene have been quantitatively analyzed in detail by applying the combination of the Activation Strain Model of reactivity and Energy Decomposition Analysis methods.
Sushmita Bhatia,Avadh Biharee,Souren Mondal et al. Sushmita Bhatia et al.
Most relevant reactions within the click chemistry framework, including copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), strain-promoted azide-alkyne cycloaddition (SPAAC), and other crucial methodologies like thiol-ene reactions are discussed along with their mechanisms.
Zemin Pan,Liying Fu,Zhilun Zhou et al. Zemin Pan et al.
The palladium-catalyzed [3 + 2] cycloaddition of vinylethylene carbonates (VECs) with ketones presents significant challenges with only sporadic examples reported....Herein, we have developed an in situ generation strategy enabling the engagement of polycarbonyl-based ketones in [3 + 2] cycloaddition with VECs.
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