2006
DOI: 10.1021/cr0500582
|View full text |Cite
|
Sign up to set email alerts
|

Polycyclic Polyprenylated Acylphloroglucinols

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

5
350
0
5

Year Published

2009
2009
2019
2019

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 486 publications
(360 citation statements)
references
References 101 publications
5
350
0
5
Order By: Relevance
“…[1][2][3] As a vast family of natural products from the Hypericum genus, PPAPs possess stunningly complex structures containing bicyclo [3.3.1]nonane, homoadamantyl and adamantyl cores. [1][2][3] Recently, a bewildering array of PPAPs derivatives with intriguing novel skeletons were characterized by natural product researchers, which were biosynthesized from conventional PPAPs through carbon migration, rearrangement, ring breakage, carbon reduction and so on. [4][5][6][7][8][9][10][11][12][13][14] Besides, driven by their fascinating and challenging structures, PPAPs have been a vibrant area in synthesis research.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3] As a vast family of natural products from the Hypericum genus, PPAPs possess stunningly complex structures containing bicyclo [3.3.1]nonane, homoadamantyl and adamantyl cores. [1][2][3] Recently, a bewildering array of PPAPs derivatives with intriguing novel skeletons were characterized by natural product researchers, which were biosynthesized from conventional PPAPs through carbon migration, rearrangement, ring breakage, carbon reduction and so on. [4][5][6][7][8][9][10][11][12][13][14] Besides, driven by their fascinating and challenging structures, PPAPs have been a vibrant area in synthesis research.…”
Section: Introductionmentioning
confidence: 99%
“…[1] The majority of PPAPs possess a characteristic perprenylated bicyclo[3.3.1]nonatrione core and interesting biological activities that alter depending on the nature of the side-chain or position of the exocyclic acyl group within the core. Within recent years a number of sophisticated synthetic approaches toward type A and type B PPAPs have been reported by the groups of Simpkins, Marazano, Shibasaki, Danishefsky, Shair, Coltart, Porco, and most recently Barriault.…”
Section: Introductionmentioning
confidence: 99%
“…They can be divided into three classes: type-A PBDs, which have a C(1) acyl group and an adjacent C(8) quaternary center; type-B PBDs, which bear a C(3) acyl group; and the rare type-C PBDs, which have a C(1) acyl group and a distant C(6) quaternary center. [20,21] In our study, four type-B PBDs (compounds 1, 3, 4 and 10) and eight type-A PBDs (compounds 2, 5-9, 11 and 12) were studied. Seven of them (compounds 5-9, 11 and 12) showed a secondary cyclization involving the hydroxylated enolic group of the core and pendant olefinic groups, affording furan-or pyrano-fused structures.…”
Section: Introductionmentioning
confidence: 99%