Cavicularin

Cavicularin

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Names
IUPAC name 9,10,18,19-Tetrahydro-5,8:15,17-diethenobenzo[g]naphth[1,8-bc]oxacyclotetradecin-3,12,21-triol
Identifiers
CAS Number	178734-41-3 Y
ChemSpider	9491133 N
Jmol 3D model	Interactive image
PubChem	11316166
InChI InChI=1S/C28H22O4/c29-20-8-11-22-18(13-20)4-1-16-2-9-21(10-3-16)32-28-25(30)12-7-17-5-6-19-14-26(31)24(22)15-23(19)27(17)28/h2-3,7-15,29-31H,1,4-6H2 N Key: MCFLLKAHGNIXPF-UHFFFAOYSA-N N InChI=1/C28H22O4/c29-20-8-11-22-18(13-20)4-1-16-2-9-21(10-3-16)32-28-25(30)12-7-17-5-6-19-14-26(31)24(22)15-23(19)27(17)28/h2-3,7-15,29-31H,1,4-6H2 Key: MCFLLKAHGNIXPF-UHFFFAOYAB
SMILES c1cc2ccc1CCc3cc(ccc3-c4cc-5c(cc4O)CCc6c5c(c(cc6)O)O2)O
Properties
Chemical formula	C28H22O4
Molar mass	422.48 g·mol−1
Vapor pressure	{{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Cavicularin is a natural phenolic secondary metabolite isolated from the liverwort Cavicularia densa. This macrocycle is unusual because it was the first compound isolated from nature displaying optical activity solely due to the presence of planar chirality and axial chirality. The specific rotation for (+)-cavicularin is +168.2°. It is also a very strained molecule. The para-substituted phenol ring is bent about 15° out of planarity, adopting a somewhat boat-like geometry. This type of angle strain in aromatic compounds is normally reserved for synthetic cyclophanes.

File:Cavicularin.png

Cavicularin, three-dimensional representation

The liverwort was obtained from Mt. Ishizuchi in the district of Shikoku. The material was dried for one day, ground to a powder and 5 grams were refluxed in methanol for 4 months to yield 2.5 mg (0.049%) of cavicularin after column chromatography and preparative TLC.

File:Riccardin C.svg

Riccardin C, flat molecule representation

Total synthesis

In 2005 and again in 2011, the compound was prepared by total synthesis together with the unstrained compound riccardin C. The strategy used was a radical reaction. In 2013 several procedures have been reported, one based on transannulation, one based on a Diels-Alder reaction and one (racemic) based on a coupling reaction.