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Squaramide-Catalyzed Enantioselective Michael Addition of Pyrazol-3- ones to ortho-Quinone Methides (Complementary material)

Repositori DSpace/Manakin

dc.contributor.author	Carceller-Ferrer, Laura
dc.contributor.author	Blay Llinares, Gonzalo
dc.contributor.author	Pedro, José Ramón
dc.contributor.author	Vila Descals, Carlos
dc.date.accessioned	2020-09-18T08:53:29Z
dc.date.available	2020-09-18T08:53:29Z
dc.date.issued	2020	es_ES
dc.identifier.citation	Squaramide-Catalyzed Enantioselective Michael Addition of Pyrazol-3- ones to ortho-Quinone Methides. Letters in Organic Chemistry, Volume 17 , Issue 11, 837. https://www.eurekaselect.com/174110/article	es_ES
dc.identifier.uri	https://hdl.handle.net/10550/75483
dc.description	Aquest document es el material suplementari del article titulat: Squaramide-Catalyzed Enantioselective Michael Addition of Pyrazol-3- ones to ortho-Quinone Methides.	es_ES
dc.description.abstract	(Complementary material)The ortho effect arises in certain electrophilic aromatic substitutions when a meta director is meta to an ortho/para director. Among the three expected isomer products, only the two isomers ortho to the meta director are produced normally. To find an explanation for the ortho effect, nitrations of two properly substituted benzenes were explored. Evidence supported an explanation based on resonance involving the meta director.	es_ES
dc.language.iso	en	es_ES
dc.title	Squaramide-Catalyzed Enantioselective Michael Addition of Pyrazol-3- ones to ortho-Quinone Methides (Complementary material)	es_ES
dc.type	other	es_ES
dc.subject.unesco	UNESCO::QUÍMICA	es_ES
dc.identifier.doi	10.2174/1876402911666190806105543	es_ES