Biosynthesis and Chemical Synthesis of Presilphiperfolanol Natural Products

被引:35
|
作者
Hong, Allen Y. [1 ]
Stoltz, Brian M. [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Warren & Katharine Schlinger Lab Chem & Chem Engn, Pasadena, CA 91125 USA
关键词
biosynthesis; natural products; structure elucidation; terpenoids; total synthesis; OCCURRING TERPENE DERIVATIVES; X-RAY-ANALYSIS; ESSENTIAL OIL; CARYOPHYLLENE DIHYDROCHLORIDE; CATALYZED 1,4-HYDROBORATION; TRICYCLIC SESQUITERPENES; UNSATURATED ALCOHOLS; ETHYL ACETOACETATE; ACIDIC MEDIA; PART II;
D O I
10.1002/anie.201309494
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Presilphiperfolanols constitute a family of biosynthetically important sesquiterpenes which can rearrange to diverse sesquiterpenoid skeletons. While the origin of these natural products can be traced to simple linear terpene precursors, the details of the enzymatic cyclization mechanism that forms the stereochemically dense tricyclic skeleton has required extensive biochemical, computational, and synthetic investigation. Parallel efforts to prepare the unique and intriguing structures of these compounds by total synthesis have also inspired novel strategies, thus resulting in four synthetic approaches and two completed syntheses. While the biosynthesis and chemical synthesis studies performed to date have provided much insight into the role and properties of these molecules, emerging questions regarding the biosynthesis of newer members of the family and subtle details of rearrangement mechanisms have yet to be explored.
引用
收藏
页码:5248 / 5260
页数:13
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