Benzylation of N-phenyl-2-phenylacetamide under microwave irradiation

Autor: DUSAN Z. MIJIN, MASA PRASCEVIC, SLOBODAN D. PETROVIC

Publikováno v: Journal of the Serbian Chemical Society, Vol 73, Iss 10, Pp 945-950 (2008)

N-Phenyl-2-phenylacetamide was alkylated with benzyl chloride in the presence of powdered potassium hydroxide under microwave irradiation in a solvent-free system. The reactions were also performed in the presence of phase-transfer catalysts. The for

Externí odkaz: https://doaj.org/article/fe96062cb3564ae7b726180080b4b7db

Alkylation of N-substituted 2-phenylacetamides

Autor: SLOBODAN D. PETROVIC, MILICA M. MISIC-VUKOVIC, DUSAN Z. MIJIN

Publikováno v: Journal of the Serbian Chemical Society, Vol 69, Iss 10, Pp 711-736 (2004)

Various N-substituted phenylacetamides were alkylated using different alkylating agents under neutral and basic conditions. Reactions were performed at different reaction temperatures and in various solvents. Also, a number of various catalysts were

Externí odkaz: https://doaj.org/article/dfa2b540ecc44f36b8e5c4e85583eda4

Benzylation of N-phenyl-2-phenylacetamide under microwave irradiation

Autor: Masa Prascevic, Dusan Z. Mijin, Slobodan D. Petrović

Publikováno v: Journal of the Serbian Chemical Society, Vol 73, Iss 10, Pp 945-950 (2008)
Journal of the Serbian Chemical Society

N-Phenyl-2-phenylacetamide was alkylated with benzyl chloride in the presence of powdered potassium hydroxide under microwave irradiation in a solvent-free system. The reactions were also performed in the presence of phase-transfer catalysts. The for

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::941b88f8d9955d3ba2836164389fbb3f
https://doi.org/10.2298/jsc0810945m

Practical and highly selective sulfur ylide-mediated asymmetric epoxidations and aziridinations using a cheap and readily available chiral sulfide: extensive studies to map out scope, limitations, and rationalization of diastereo- and enantioselectivities

Autor: Mairi F. Haddow, C. Chun Chen, Ona Illa, Eoghan M. McGarrigle, Mehrnoosh Ostovar, Varinder K. Aggarwal, Matteo Lusi, Chandreyee Saha, Sophie Nocquet-Thibault, Mariam Namutebi

Publikováno v: Illa Soler, O, Namutebi, M, Saha, C, Ostovar, M, Chen, C-C, Haddow, M F, Nocquet-Thibault, S, Lusi, M, McGarrigle, E M & Aggarwal, V K 2013, ' Practical and Highly Selective Sulfur Ylide-Mediated Asymmetric Epoxidations and Aziridinations Using a Cheap and Readily Available Chiral Sulfide: Extensive Studies To Map Out Scope, Limitations, and Rationalization of Diastereo-and Enantioselectivities ', Journal of the American Chemical Society, vol. 135, no. 32, pp. 11951-11966 . https://doi.org/10.1021/ja405073w

The chiral sulfide, isothiocineole, has been synthesized in one step from elemental sulfur, gamma-terpinene, and limonene in 61% yield. A mechanism involving radical intermediates for this reaction is proposed based on experimental evidence. The appl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46c7d0bd3706c7b4c52f9ad7f4f3360d
https://pubmed.ncbi.nlm.nih.gov/23902598

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