Synthesis of dihydrogambirtannine by alkyne [2 + 2 + 2]-cyclotrimerisation
The first asymmetric synthesis of (−)-dihydrogambirtannine has been achieved using nucleophilic addition to a chiral sulfinyl imine to establish the stereogenic centre and [2 + 2 + 2] alkyne cyclotrimerisation to construct the aromatic E ring.
Saved in:
Main Authors: | Seankongsuk, Pattarakiat, Sae-Lao, Patcharaporn, He, Shi, Pereira, Veronica, Bates, Roderick W. |
---|---|
其他作者: | School of Chemistry, Chemical Engineering and Biotechnology |
格式: | Article |
語言: | English |
出版: |
2025
|
主題: | |
在線閱讀: | https://hdl.handle.net/10356/182986 |
標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|
機構: | Nanyang Technological University |
語言: | English |
相似書籍
-
Synthesis of Mycobacterium tuberculosis ATP synthase inhibitors
由: Pattarakiat, Seankongsuk
出版: (2022) -
Confirmation of the structure of (±)-preisomide by total synthesis
由: Teo, Hong Kang, et al.
出版: (2024) -
Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines
由: Kumaran, Elumalai, et al.
出版: (2014) -
Towards the stereoselective synthesis of bicyclic and tricyclic alkaloid natural products
由: Patcharaporn Sae-Lao
出版: (2012) -
[Cp*RhCl2]2-catalyzed alkyne hydroamination to 1,2-dihydroquinolines
由: Kumaran, Elumalai, et al.
出版: (2015)