التفاصيل البيبلوغرافية
العنوان: |
One-Pot Preparation of Bridged Tricyclic and Fused Tetracyclic Scaffolds via Rhodium(III)-Catalyzed Asymmetric Borylative Cyclization |
المؤلفون: |
Qing-Hua Li, Dingding Gao, Cheng-Yu He, Qi Liao, Yun-Xuan Tan, Yu-Hui Wang, Rui Ding, Guo-Qiang Lin, Ping Tian |
المصدر: |
Cell Reports Physical Science, Vol 1, Iss 10, Pp 100222- (2020) |
بيانات النشر: |
Elsevier, 2020. |
سنة النشر: |
2020 |
المجموعة: |
LCC:Physics |
مصطلحات موضوعية: |
Physics, QC1-999 |
الوصف: |
Summary: Bridged and fused polycyclic structures are found in a huge number of natural products. Significant progress has been made on their syntheses; however, facile and practical strategies to afford polycycles with tunable substituents and functional groups remain rare. Here, we report a practical rhodium(III)-catalyzed asymmetric borylative cyclization of cyclohexadienone-containing 1,6-enynes, affording highly enantioenriched cis-bicyclic frameworks with great functional group compatibility, and further extend it to construct bridged tricyclic and fused tetracyclic skeletons in one-pot protocols. The combination of borylative cyclization with a subsequent oxidation/aldol reaction sequence goes through an epimerization of the stereocenter adjacent to the acetyl group, yielding various tricyclic compounds. In addition, borylative cyclization is combined with a Suzuki-Miyaura coupling/Michael addition sequence, leading to diverse tetracyclic compounds. Starting from simple starting materials, both one-pot transformations yield complex products bearing several consecutive stereocenters with excellent enantioselectivities. Furthermore, an unnatural steroid-like compound is also readily prepared, demonstrating the potential of this methodology. |
نوع الوثيقة: |
article |
وصف الملف: |
electronic resource |
اللغة: |
English |
تدمد: |
2666-3864 |
Relation: |
http://www.sciencedirect.com/science/article/pii/S266638642030237X; https://doaj.org/toc/2666-3864 |
DOI: |
10.1016/j.xcrp.2020.100222 |
URL الوصول: |
https://doaj.org/article/8968a8f4a05b4d878bc7f978718e5cc6 |
رقم الانضمام: |
edsdoj.8968a8f4a05b4d878bc7f978718e5cc6 |
قاعدة البيانات: |
Directory of Open Access Journals |