H-Bond-Directing Organocatalyst for Enantioselective [4+2] Cycloadditions via Dienamine Catalysis

التفاصيل البيبلوغرافية
العنوان: H-Bond-Directing Organocatalyst for Enantioselective [4+2] Cycloadditions via Dienamine Catalysis
المؤلفون: Shoulei Wang, Carles Rodríguez-Escrich, Miquel A. Pericàs
المصدر: Recercat. Dipósit de la Recerca de Catalunya
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بيانات النشر: ACS Publications, 2016.
سنة النشر: 2016
مصطلحات موضوعية: 010405 organic chemistry, Stereochemistry, Hydrogen bond, Organic Chemistry, Hydroxy group, Enantioselective synthesis, 010402 general chemistry, 01 natural sciences, Biochemistry, Cycloaddition, 0104 chemical sciences, Stereocenter, Catalysis, chemistry.chemical_compound, chemistry, Stereoselectivity, Physical and Theoretical Chemistry, Heterocyclic derivatives
الوصف: An efficient, highly regio- and stereoselective [4 + 2] cycloaddition reaction to generate tetrahydropyranopyrazole frameworks has been developed. To this end, a dienamine-based catalytic strategy that relies on the H-bond-directing effect of the hydroxy group of a dinaphthylprolinol-type aminocatalyst has been used. This enables the synthesis of multifunctionalized heterocyclic derivatives with three contiguous stereocenters in good yields and excellent enantioselectivities.
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cf1eefa13ba983ce393698e88001e10Test
http://hdl.handle.net/2072/226233Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....5cf1eefa13ba983ce393698e88001e10
قاعدة البيانات: OpenAIRE