Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Vitaly A. Shcherbinin"'
Publikováno v:
Proceedings, Vol 9, Iss 1, p 21 (2019)
An efficient method is proposed for N-adamantylation of primary carboxamides and sulfonamides, ethyl carbamate, and 4-nitroaniline using the stoichiometric amount of 1-adamantanol in the presence of 5 mol% aluminum triflate in nitromethane. Similarit
Externí odkaz:
https://doaj.org/article/5b6914a7fbfe4a80a263d86e7a38e280
Autor:
Vitaly A. Shcherbinin, V. V. Konshin
Publikováno v:
Tetrahedron. 75:3570-3578
An efficient method for the synthesis of O-substituted mandelic acids containing alkenyl, alkynyl, methoxycarbonyl, or phenacyl fragments via the Lewis acid-catalyzed reaction of 1,3-dioxolan-4-ones with different C-nucleophiles is proposed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e16b187ceb4513cebed816597e7ad6ea
https://doi.org/10.1016/j.tet.2019.05.025
https://doi.org/10.1016/j.tet.2019.05.025
Autor:
Vitaly A. Shcherbinin, V. V. Konshin
Publikováno v:
Tetrahedron Letters. 59:3005-3009
The reactions of 1,3-dioxolan-4-ones, readily available from α-hydroxy acids and aldehydes, with C-nucleophiles are described. Two possible reaction pathways resulting in O-substituted acids and tri-(hetero)arylmethanes are shown.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2712d593807c6cee89f4a1021232b68
https://doi.org/10.1016/j.tetlet.2018.06.060
https://doi.org/10.1016/j.tetlet.2018.06.060
Publikováno v:
Proceedings, Vol 9, Iss 1, p 21 (2019)
An efficient method is proposed for N-adamantylation of primary carboxamides and sulfonamides, ethyl carbamate, and 4-nitroaniline using the stoichiometric amount of 1-adamantanol in the presence of 5 mol% aluminum triflate in nitromethane. Similarit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e95f0f2f385264e859f13948147922b7
https://doi.org/10.3390/ecsoc-22-05661
https://doi.org/10.3390/ecsoc-22-05661
Publikováno v:
22nd International Electronic Conference on Synthetic Organic Chemistry.
There are several methods for the synthesis of 2-(1-adamantyl)furans, including those based on 1-adamantoyl chloride and malonic ester; 5-nitrofuran-2-carboxylic acid and 1-adamantanecarboxylic acid; 1-adamantylcarbaldehyde and propargylmagnesium bro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5acd499fc47dca7b77ca59d87ca60622
https://doi.org/10.3390/ecsoc-22-05667
https://doi.org/10.3390/ecsoc-22-05667
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1768-1771
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59c7e731413eb76b35aa297b7e434675
https://doi.org/10.1007/s10593-015-1649-x
https://doi.org/10.1007/s10593-015-1649-x
Publikováno v:
Tetrahedron Letters. 57:1483-1485
A new tandem transformation of 3-furylphthalides into 3-(3-oxoalkyl)isocoumarins mediated by a red phosphorus/iodine reagent system has been developed. This allows the straightforward preparation of functionalized isocoumarins in good yields using re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a2fada57b265ab083d338964ad216ad
https://doi.org/10.1016/j.tetlet.2016.02.072
https://doi.org/10.1016/j.tetlet.2016.02.072
Publikováno v:
Tetrahedron Letters. 57:1473-1475
A CuBr 2 catalyzed synthesis of 3-furylphthalides was accomplished by a dehydrative coupling reaction between phthalaldehydic acids and furans. The devised synthetic procedure has a broad substrate scope and mild reaction conditions and employs a rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4949c194ab6e5611f3c5c6a9701d7da9
https://doi.org/10.1016/j.tetlet.2016.02.070
https://doi.org/10.1016/j.tetlet.2016.02.070
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:619-633
A systematic summary is presented for methods for the synthesis of naphtho[2,3-b]furans developed over the past twenty years. Natural occurrence of these compounds as well as their biological activity and transformations are reviewed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cbce3dd3a8cbbe993d1b9d0fcf252cf
https://doi.org/10.1007/s10593-014-1515-2
https://doi.org/10.1007/s10593-014-1515-2
Publikováno v:
ChemInform. 47
A CuBr 2 catalyzed synthesis of 3-furylphthalides was accomplished by a dehydrative coupling reaction between phthalaldehydic acids and furans. The devised synthetic procedure has a broad substrate scope and mild reaction conditions and employs a rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72bade4af96b6b7a200471ab102e0300
https://doi.org/10.1002/chin.201629125
https://doi.org/10.1002/chin.201629125