مورد إلكتروني

Enantioselective synthesis of 3-hydroxy- and 3-amino-3-alkynyl-2-oxindoles by the dimethylzinc-mediated addition of terminal alkynes to isatins and isatin-derived ketimines

التفاصيل البيبلوغرافية
العنوان: Enantioselective synthesis of 3-hydroxy- and 3-amino-3-alkynyl-2-oxindoles by the dimethylzinc-mediated addition of terminal alkynes to isatins and isatin-derived ketimines
بيانات النشر: The Royal Society of Chemistry 2023
تفاصيل مُضافة: Prieto, Elena
نوع الوثيقة: Electronic Resource
مستخلص: Producción Científica
A common protocol for enantioselective alkynylation of isatins and isatin-derived ketimines using terminal alkynes and Me2Zn in the presence of a catalytic amount of a chiral perhydro-1,3-benzoxazine with moderate to excellent enantioselectivity under mild reaction conditions is described. The additions to ketimines present a novel approach to chiral amines being derivatives of oxindoles. The reaction is broad in scope with respect to aryl- and alkyl-substituted terminal alkynes and isatin derivatives. In isatins, the alkynylation occurs at the Si face of the carbonyl group, whereas in the ketimine derivatives it occurs at the Re face of the imine.
Junta de Castilla y León, proyectos FEDER-VA115P17 y VA149G18
مصطلحات الفهرس: Catálisis enantioselectiva, compuestos organozíncicos, alquinilación, isatinas e iminas derivadas de isatinas, 2306.99 Química Orgánica-Síntesis enatioselectiva, info:eu-repo/semantics/article, info:eu-repo/semantics/acceptedVersion
URL: http://worldcat.org/search?q=on:ESUDE+http://uvadoc.uva.es/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL
https://pubs.rsc.org/en/content/articlelanding/2023/ob/d3ob01023f
https://pubs.rsc.org/en/content/articlelanding/2023/ob/d3ob01023f
الإتاحة: Open access content. Open access content
info:eu-repo/semantics/openAccess
The Royal Society of Chemistry
ملاحظة: application/pdf
Spanish
أرقام أخرى: ESUDE oai:uvadoc.uva.es:10324/63063
https://doi.org/10.1039/d3ob01023f
Organic and Biomolecular. Chemistry, 2023, vol.21, n 34, p 6940-69-48
1477-0520
https://uvadoc.uva.es/handle/10324/63063
6940
34
6948
Organic & Biomolecular Chemistry
21
1477-0539
1415715708
المصدر المساهم: UNIVERSIDAD DE VALLADOLID
From OAIster®, provided by the OCLC Cooperative.
رقم الأكسشن: edsoai.on1415715708
قاعدة البيانات: OAIster