ChemInform Abstract: Expedient Synthesis of the Tetracyclic Core (II) of ent-Nakadomarin A (III).

ChemInform ◽  
2008 ◽  
Vol 39 (37) ◽  
Author(s):  
Haibing Deng ◽  
Xiaobao Yang ◽  
Zhaolong Tong ◽  
Zhong Li ◽  
Hongbin Zhai
Keyword(s):  
Nakadomarin A ◽  
Tetracyclic Core

Synthetic approach towards nakadomarin A: efficient synthesis of the central tetracyclic core

2001 ◽  
Vol 42 (47) ◽  
pp. 8345-8349 ◽  
Author(s):  
Toshiaki Nagata ◽  
Atsushi Nishida ◽  
Masako Nakagawa
Keyword(s):  
Synthetic Approach ◽  
Efficient Synthesis ◽  
Nakadomarin A ◽  
Tetracyclic Core

Synthesis of the Tetracyclic Core Structure of (±)-Nakadomarin A through Azomethine Ylide-Alkene [3+2] Cycloaddtion

2013 ◽  
Vol 2 (7) ◽  
pp. 561-564 ◽  
Author(s):  
Fufang Wu ◽  
Yanhe Chen ◽  
Bin Cheng ◽  
Yun Li ◽  
Hongbin Zhai
Keyword(s):  
Core Structure ◽  
Azomethine Ylide ◽  
Nakadomarin A ◽  
Tetracyclic Core

Expedient Synthesis of the Tetracyclic Core ofent-Nakadomarin A

2008 ◽  
Vol 10 (9) ◽  
pp. 1791-1793 ◽  
Author(s):  
Haibing Deng ◽  
Xiaobao Yang ◽  
Zhaolong Tong ◽  
Zhong Li ◽  
Hongbin Zhai
Keyword(s):  
Nakadomarin A ◽  
Tetracyclic Core

Synthesis of Spongidine A, D and Petrosaspongiolide L Methyl Ester Using Pyridine C-H Functionalization

2019 ◽  
Author(s):  
Florian Bartels ◽  
Manuela Weber ◽  
Mathias Christmann
Keyword(s):  
Natural Products ◽  
Methyl Ester ◽  
Hydrogen Atom ◽  
Phospholipase A2 ◽  
Late Stage ◽  
Hydrogen Atom Transfer ◽  
Ring System ◽  
Tetracyclic Core ◽  
Intramolecular Hydrogen ◽  
Phospholipase A2 Inhibitors

<div>An efficient strategy for the synthesis of the potent phospholipase A2 inhibitors spongidine A and D is presented. The tetracyclic core of the natural products was assembled via an intramolecular hydrogen atom transfer‐initiated Minisci reaction. A divergent late‐stage functionalization of the tetracyclic ring system was also used to achieve a concise synthesis of petrosaspongiolide L methyl ester.</div>

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