Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Munchnones"'
Publikováno v:
Radiation Effects and Defects in Solids. 175:730-744
Techniques in polymer synthesis are taking different dimensions in the last few decades. Reversible-deactivation radical polymerization processes resulted in a wide range of polymeric architectures...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02fff3f9e8e2c557948eaf03d1f7819d
https://doi.org/10.1080/10420150.2020.1759066
https://doi.org/10.1080/10420150.2020.1759066
Publikováno v:
De Castro, P P, Batista, G M F, Amarante, G W & Dos Santos, H F 2021, ' Origin of Enantioselectivity in Chiral Phosphoric-Acid-Catalyzed Azlactone Dynamic Kinetic Resolution ', Journal of Organic Chemistry, vol. 86, no. 18, pp. 13169-13174 . https://doi.org/10.1021/acs.joc.1c01882
Theoretical calculations, associated with control experiments, were carried out to gain insights into the mechanism and origin of enantioselectivity in the phosphoric-acid-catalyzed dynamic kinetic resolution of azlactones. The results revealed a Mü
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b68da62ec8c2a64f8cd694fef55a257a
https://pure.au.dk/portal/da/publications/origin-of-enantioselectivity-in-chiral-phosphoricacidcatalyzed-azlactone-dynamic-kinetic-resolution(d6059e04-7a12-45bb-837b-96cffb72d636).html
https://pure.au.dk/portal/da/publications/origin-of-enantioselectivity-in-chiral-phosphoricacidcatalyzed-azlactone-dynamic-kinetic-resolution(d6059e04-7a12-45bb-837b-96cffb72d636).html
Publikováno v:
Molecules, Vol 10, Iss 9, Pp 1109-1118 (2005)
A series of previously unavailable derivatives of 2-alkyl- and 2-benzylderivatives of oxazolo[3,2-a]pyridines III were obtained via tandem ring opening and ring closure from stable mesoionic 3-acyloxazolo[3,2-a]pyridinium-2-olates I. The key intermed
Externí odkaz:
https://doaj.org/article/5a5d61d40e724ac1b2b886108dc3f628
Publikováno v:
Bioorganic & Medicinal Chemistry Letters, 10(3), 389-392. American Chemical Society
ACS Medicinal Chemistry Letters
ACS Medicinal Chemistry Letters
A concise and convergent synthesis of the atorvastatin, the best-selling cardiovascular drug of all time, is presented. Our approach is based on an Ugi reaction, which shortens the current synthetic route and is advantageous over the published synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4dc00503065727ae572f9ea6b94d81d
https://doi.org/10.1021/acsmedchemlett.8b00579
https://doi.org/10.1021/acsmedchemlett.8b00579
Autor:
Masami Kawase, Ryosuke Saijo
Publikováno v:
European Journal of Organic Chemistry. 2019:1535-1541
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0926f2a85c5fb5a1dbe99f1a8ba9e18e
https://doi.org/10.1002/ejoc.201801728
https://doi.org/10.1002/ejoc.201801728
Akademický článek
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Akademický článek
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Autor:
E. S. Meshcheryakova, A. A. Fatykhov, Z. A. Ibatullina, Leonard M. Khalilov, Rail R. Gataullin
Publikováno v:
Russian Journal of Organic Chemistry. 53:697-708
Intramolecular [3+2]-cycloaddition was studied of munchnones generated at heating syn- and anti-atropisomers of N-acyl-N-[6-methyl-2-(cyclopent-2-en-1-yl)phenyl]glycines with acetic anhydride. By spectral and X-ray diffraction analysis syn-isomers of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9295da2e4dbf6de6e9e821e9c7c10354
https://doi.org/10.1134/s1070428017050098
https://doi.org/10.1134/s1070428017050098
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:926-928
The microreview describes recent advances in the synthesis of isoindole derivatives via pyrrole ring closure reactions. We report the latest selected examples (2012–2018) on the synthesis of isoindoles: multicomponent reactions, [3+2] cycloaddition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e61456cf892a854ead1aa14e14161462
https://doi.org/10.1007/s10593-018-2371-2
https://doi.org/10.1007/s10593-018-2371-2
Publikováno v:
European Journal of Organic Chemistry. 2016:2789-2792
A family of stabilized munchnones bearing an acyl group at C4 have been prepared and studied in alkyne cycloaddition reactions. These reactions are highly regioselective, and the method represents a rapid and straightforward route to densely substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76b2f0a79e93c796957290ef5354b1f8
https://doi.org/10.1002/ejoc.201600486
https://doi.org/10.1002/ejoc.201600486