دورية أكاديمية

De-epimerizing DyKAT of β-Lactones Generated by Isothiourea-Catalysed Enantioselective [2+2] Cycloaddition

التفاصيل البيبلوغرافية
العنوان: De-epimerizing DyKAT of β-Lactones Generated by Isothiourea-Catalysed Enantioselective [2+2] Cycloaddition
المؤلفون: Conboy, Aífe, Goodfellow, Alister S., Kasten, Kevin, Dunne, Joanne, Cordes, David Bradford, Buehl, Michael, Smith, Andrew D
المصدر: Chemical Science ; ISSN 2041-6520 2041-6539
بيانات النشر: Royal Society of Chemistry (RSC)
سنة النشر: 2024
الوصف: Moderate diastereoselectivity (typically 70:30 dr) is observed in the isothiourea-catalysed [2+2]-cycloaddition of C(1)-ammonium enolates with pyrazol-4,5-diones to generate spirocyclic β lactones, but subsequent ring-opening with morpholine generatesβ hydroxyamide products with...
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1039/d4sc01410c
الإتاحة: https://doi.org/10.1039/d4sc01410cTest
http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC01410CTest
حقوق: http://creativecommons.org/licenses/by/3.0Test/
رقم الانضمام: edsbas.771EDE11
قاعدة البيانات: BASE