Results 31 to 40 of about 49,489 (310)

Decarboxylative Triazolation Enables Direct Construction of Triazoles from Carboxylic Acids

JACS Au, 2023
Triazoles have major roles in chemistry, medicine, and materials science, as centrally important heterocyclic motifs and bioisosteric replacements for amides, carboxylic acids, and other carbonyl groups, as well as some of the most widely used linkers in click chemistry.
Hang T. Dang, Viet D. Nguyen, Graham C. Haug, Hadi D. Arman, Oleg V. Larionov   +4 more
openaire   +2 more sources

Rhodium(II)-catalyzed stereocontrolled synthesis of dihydrofuran-3-imines from 1-Tosyl-1,2,3-triazoles [PDF]

, 2014
Rhodium(II) acetate catalyzes the denitrogenative transformation of 5-substituted and 4,5-disubstituted 1-sulfonyl-1,2,3-triazoles with pendent allyl and propargyl ether motifs to oxonium ylides that undergo [2,3]-sigmatropic rearrangement to give ...
Alford J. S., Alistair Boyer, Appel R., Boultwood T., Boyer J. H., Cen-Pacheco F., Chattopadhyay B., Chattopadhyay B., Chuprakov S., Chuprakov S., Chuprakov S., Clark J. S., Clark J. S., Clark J. S., Clark J. S., Clark J. S., Clark J. S., Clark J. S., Clark J. S., Culhane J. C., Dimroth O., Doyle M. P., Eberlein T. H., Ferris L., Fu J., Grimster N., Han M., Hisham A., Horneff T., Hyatt I. F. D., Jackson K. L., Jiang-Nan P., Kim S. H., Lavie D., Liu R., Lorente A., Meza-Aviña M. E., Meza-Aviña M. E., Miura T., Miura T., Miura T., Miura T., Miura T., Murphy G. K., Murphy G. K., Pan L., Parr B. T., Parr B. T., Pirrung M. C., Pirrung M. C., Raushel J., Roskamp E. J., Schultz E. E., Selander N., Selander N., Selander N., Shi Y., Suzuki T., Weinreb S. M., West F. G., West F. G., Yadagiri D., Ye T., Yoo E. J., Zibinsky M.   +64 more
core   +1 more source

Synthesis Of 2-Benzamidomethyl-5-Substituted Amino-1,3,4-Thiadiazoles-2,5-Disubstituted 1,3,4-Oxadiazole and 4,5-Disubstituted 1,2,4-Triazole-3-Thiol [PDF]

مجلة التربية والعلم, 2012
In this paper the synthesis of some substituted 1,3,4-oxadiazoles , 1,3,4-thiadiazoles and 1,2,4-triazoles starting from amino acid and benzoyl chloride is reported.
K. M. Daoud, A. N. Ali, A. A. Ahmed
doaj   +1 more source

Ground-state phases in antiferromagnetic spin-crossover chains [PDF]

Phys. Rev. B 71, 224414 (2005), 2004
Spin-crossover molecules having a low-spin ground state and a low-lying excited high-spin state are promising components for molecular electronics. We theoretically examine one-dimensional spin-crossover chain molecules of the type of Fe-II triazole complexes.
arxiv   +1 more source

Coordinatively unsaturated ruthenium complexes as efficient alkyne-azide cycloaddition catalysts [PDF]

, 2012
The performance of 16-electron ruthenium complexes with the general formula Cp*Ru(L)X (in which L = phosphine or N-heterocyclic carbene ligand; X = Cl or OCH2CF3) was explored in azide−alkyne cycloaddition reactions that afford the 1,2,3- triazole ...
Broggi, Julie, Cavallo, Luigi, Fortman, George C., Lamberti, Marina, Nolan, Steven P., Poater, Albert, Slawin, Alexandra M. Z.   +6 more
core   +2 more sources

Palladium-Catalyzed C–H Arylation of 1,2,3-Triazoles

Molecules, 2016
Palladium(II) acetate, in combination with triphenylphosphine, catalyzes direct arylation of 1,4-disubstituted 1,2,3-triazoles effectively. This C–H arylation reaction provides facile access to fully substituted triazoles with well-defined regiochemistry.
Chengwei Zhang, Lin You, Chuo Chen
doaj   +1 more source

Triazoles Synthesis & Applications as Nonsteroidal Aromatase Inhibitors for Hormone-Dependent Breast Cancer Treatment

Heteroatom Chemistry, 2022
In the last few years, nonsteroidal aromatase inhibitors (AIs) have been emerged as promising agents for treating hormone-dependent breast cancer in postmenopausal women because of their inhibitory effect on estrogen synthesis.
Huda R. M. Rashdan, Ihsan A. Shehadi
doaj   +1 more source

1,2,3-Triazole-4(5)-amines – Convenient Synthetic Blocks for the Construction of Triazolo-Annulated Heterocycles

Журнал органічної та фармацевтичної хімії, 2022
Aim. To analyze and summarize the synthetic potential of 1,2,3-triazole-4(5)-amines as efficient building blocks in the synthesis of triazolo-annulated pyridine, azine and azepine systems. Results and discussion.
Natalia O. Syrota, Sergiy V. Kemskiy, Lesya M. Saliyeva, Mykhailo V. Vovk   +3 more
doaj   +1 more source

Computationally motivated synthesis and enzyme kinetic evaluation of N-(β-d-glucopyranosyl)-1,2,4-triazolecarboxamides as glycogen phosphorylase inhibitors [PDF]

, 2015
Following our recent study of N-(β-D-glucopyranosyl)-oxadiazole-carboxamides (Polyák et al., Biorg. Med. Chem. 2013, 21, 5738) revealed as moderate inhibitors of glycogen phosphorylase (GP), in silico docking calculations using Glide have been performed ...
Alex, Arunan, Benltifa, Bokor, Broggini, Brownlee, Carta, Cheng, Cho, Chrysina, Condi, Danaei, Docsa, Fischer, Francl, Friesner, Hayes, Hayes, Hehre, Huisgen, Huisgen, Huisgen, Jorgensen, Jorgensen, Kaminski, Kantsadi, Kantsadi, Kenny, Koldobskii, Kun, Lagorce, Lipinski, Lonsdale, Marten, Murray, Murray, Nagy, Nagy, Oikonomakos, Paolini, Polya, Polyák, Pospisil, Potts, Potts, Smith, Somsák, Somsák, Somsák, Somsák, Still, Tannor, Veber, Woon, Zhao, Zhong, Zhou, Ősz   +57 more
core   +1 more source

Efecto del Butóxido de Piperonilo y Sus Mezclas con Fungicidas Triazoles sobre el Crecimiento In Vitro de Mycosphaerella fijiensis Morelet

Revista Tecnológica, 2013
Se evaluó el efecto del Butóxido de Piperonilo (BOP), un conocido sinergista de insecticidas, sobre el crecimiento micelial de Mycosphaerella fijiensis para validar la hipótesis que supone que este compuesto posee un efecto antifúngico debido a sus ...
Daniel Navia, Haydeé Torres, Miguel Quilambaqui   +2 more
doaj   +4 more sources