Total synthesis of ent-(-)-azonazine using a biomimetic direct oxidative cyclization and structural reassignment of natural product

被引:24
|
作者
Zhao, Ji-Chen [1 ]
Yu, Shun-Ming [1 ]
Qiu, Hai-Bo [1 ]
Yao, Zhu-Jun [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomimetic synthesis; Azonazine; Stereochemical assignment; Oxidative cyclization; Hypervalent iodine; ELECTROCHEMICAL OXIDATION; REAGENTS; ETHERS;
D O I
10.1016/j.tet.2014.03.061
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A biomimetic approach has been investigated and developed for the total synthesis of azonazine, an unusual marine natural cyclopeptide containing a rigid transannular 10-membered ring. A hypervalent iodine-mediated direct oxidative cyclization was successfully developed and applied to construct the highly strained core, which was the key step in the first total synthesis of ent-(-)-azonazine. Based on the physical evidences of synthesized diastereomer and enantiomer of azonazine, both the relative and absolute configurations of the natural product were revised. Two fluorinated azonazine derivatives were also synthesized in short convenient steps utilizing the same intermediate in this work. The established total synthesis opens a potential opportunity to study the structure activity relationship of natural azonazine. (c) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3197 / 3210
页数:14
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