دورية أكاديمية
De-epimerizing DyKAT of β-Lactones Generated by Isothiourea-Catalysed Enantioselective [2+2] Cycloaddition
العنوان: | De-epimerizing DyKAT of β-Lactones Generated by Isothiourea-Catalysed Enantioselective [2+2] Cycloaddition |
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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 generatesβ 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 |
DOI: | 10.1039/d4sc01410c |
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