Academic Journal

Catalytic Enantioselective Synthesis of Naturally Occurring Butenolides via Hetero-Allylic Alkylation and Ring Closing Metathesis

التفاصيل البيبلوغرافية
العنوان: Catalytic Enantioselective Synthesis of Naturally Occurring Butenolides via Hetero-Allylic Alkylation and Ring Closing Metathesis
المؤلفون: Mao, Bin, Geurts, Koen, Fañanás-Mastral, Martín, Zijl, Anthoni W. van, Fletcher, Stephen P., Minnaard, Adriaan J., Feringa, Bernard
المصدر: Mao , B , Geurts , K , Fañanás-Mastral , M , Zijl , A W V , Fletcher , S P , Minnaard , A J & Feringa , B 2011 , ' Catalytic Enantioselective Synthesis of Naturally Occurring Butenolides via Hetero-Allylic Alkylation and Ring Closing Metathesis ' , Organic letters , vol. 13 , no. 5 , pp. 948-951 . https://doi.org/10.1021/ol102994q
سنة النشر: 2011
المجموعة: University of Groningen research database
مصطلحات موضوعية: TRANS-WHISKEY LACTONE, (+)-NEPHROSTERANIC ACID, (-)-ROCCELLARIC ACID, (+)-TRANS-WHISKEY LACTONE, (+)-TRANS-COGNAC LACTONE, PARACONIC ACIDS, GAMMA-LACTONES, ASYMMETRIC DIHYDROXYLATION, (-)-NEPHROSTERANIC ACID, (+)-ROCCELLARIC ACID
الوصف: An efficient catalytic asymmetric synthesis of chiral γ-butenolides was developed based on the hetero-allylic asymmetric alkylation (h-AAA) in combination with ring closing metathesis (RCM). The synthetic potential of the h-AAA-RCM protocol was illustrated with the facile synthesis of (-)-whiskey lactone, (-)-cognac lactone, (-)-nephrosteranic acid, and (-)-roccellaric acid.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
DOI: 10.1021/ol102994q
الاتاحة: https://hdl.handle.net/11370/6dc5ecc8-f9e5-4e0f-b8fd-63f1f797667c
https://research.rug.nl/en/publications/6dc5ecc8-f9e5-4e0f-b8fd-63f1f797667c
https://doi.org/10.1021/ol102994q
https://pure.rug.nl/ws/files/2504531/2011OrgLettMaoSupp.pdf
https://pure.rug.nl/ws/files/2504532/2011OrgLettMao.pdf
Rights: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.98C08313
قاعدة البيانات: BASE