Naturally Occurring Dimers from Chemical Perspective

被引:59
|
作者
Lian, Gaoyan [1 ]
Yu, Biao [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China
关键词
OKINAWAN MARINE SPONGE; STEREOISOMERIC TRITERPENE DIMERS; POTENT CYTOTOXIC MACROLIDE; SWINHOLIDE-A; BISINDOLE ALKALOIDS; INDOLE ALKALOIDS; STEREOCONTROLLED SYNTHESIS; ABSOLUTE STEREOSTRUCTURE; CHLORANTHACEAE PLANTS; BIOMIMETIC SYNTHESIS;
D O I
10.1002/cbdv.201000038
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have presented here an overview of the recently reported dimeric natural products and described their possible biosynthesis pathways. Usually, for a class of compounds from similar sources, a general biosynthesis pathway is proposed; a common monomer has usually been indicated as the biosynthetic precursor. Various structural modifications (e.g., oxidation, rearrangement, cyclization, etc.) on the monomer or after dimerization increase the diversity of dimers. In some cases, biomimetic syntheses towards a particular dimer have been realized, thus supporting (figure presented) the proposed biosynthesis pathways. In many others, the biosynthetic pathways are highly speculative. Nature continuously provides unusual dimeric compounds that shall inspire chemists to explore the amazing 'natural' dimerization pathways. © 2010 Verlag Helvetica Chimica Acta AG, Zürich.
引用
收藏
页码:2660 / 2691
页数:32
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