User:Sdsulliv/sandbox

Sdsulliv/sandbox
Names
	IUPAC name (2Z,5S,11S,12S)-12-Hydroxy-11-isopropenyl-3,14-dimethyl-6,16-dioxatricyclo[11.2.1.15,8]heptadeca-1(15),2,8(17),13-tetraen-7-one
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	10213404;
	InChI InChI=1S/C20H24O4/c1-11(2)17-6-5-14-10-16(24-20(14)22)8-12(3)7-15-9-13(4)19(23-15)18(17)21/h7,9-10,16-18,21H,1,5-6,8H2,2-4H3/b12-7-/t16-,17-,18-/m0/s1 Key: RCFMTOJVVOOMTO-PVUOXGCVSA-N;
	SMILES Cc1cc/2oc1[C@H]([C@@H](CCC3=C[C@H](C/C(=C2)/C)OC3=O)C(=C)C)O;
Properties
Chemical formula	C20H28O3
Molar mass	328.40216
Melting point	140-142°C
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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Bipinnatin J is a diterpene isolated from Pseudopterogorgia bipinnata found in the Eastern Caribbean Sea.^[1] It is one of the structurally simplest of the furanocembrenolides, and is speculated to be a biosynthetic precursor to a wide array cembrenolides along with the dehydroxylated analog, rubifolide. ^[2]

Biosynthesis

Although the exact biosynthesis of Bipinnatin J has not been formally studied, the biosynthesis the core cembrane skeleton, neo-cembrene, has been extensively studied. Starting from Geranylgeranyl pyrophosphate, the pyrophosphate leaves, creating the allyl carbocation. A type A cyclization then yields the 14-membered cembrane ring with the isopropyl cation outside the ring. Proton elimination then yields neo-cembrene. ^[3] From this point, the biosynthesis of Bipinnatin J is speculative. Oxidation, most likely utilizing P450 monooxygenases, followed by ring closure creates both the furan and butenolide within the 14-membered ring. ∆ double bond isomerization of the C7-C8 olefin then occurs to afford the Z conformation, yielding rubifolide. Another oxidation of C2 then yields bipinnatin J. ^[2]

Proposed biosynthesis of bipinnatin J

References

^ Rodriguez, A. D.; Shi, J.-G. (1998). "The First Cembrane-Pseudopterane Cycloisomerization". J. Org. Chem. 63 (2): 420–421. doi:10.1021/jo971884g.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ ^a ^b Roethle, P. A.; Trauner, D. (2008). "The chemistry of marine furanocembranoids, pseudopteranes, gersolanes, and related natural products". Nat. Prod. Rep. 25 (2): 298–317. doi:10.1039/b705660p.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ MacMillan, J.; Beale, M. H. (1999). "Diterpene Biosynthesis". Comprehensive Natural Products Chemistry. 2: 217–243.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[1] Rodriguez, A. D.; Shi, J.-G. (1998). "The First Cembrane-Pseudopterane Cycloisomerization". J. Org. Chem. 63 (2): 420–421. doi:10.1021/jo971884g.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[Trauner-2] Roethle, P. A.; Trauner, D. (2008). "The chemistry of marine furanocembranoids, pseudopteranes, gersolanes, and related natural products". Nat. Prod. Rep. 25 (2): 298–317. doi:10.1039/b705660p.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[3] MacMillan, J.; Beale, M. H. (1999). "Diterpene Biosynthesis". Comprehensive Natural Products Chemistry. 2: 217–243.{{cite journal}}: CS1 maint: multiple names: authors list (link)

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