Elisabethatriene

Elisabethatriene
Names
	IUPAC name (1R,4S,4aR)-4-Methyl-1-[(2S)-6-methylhept-5-en-2-yl]-7-methylidene-2,3,4,4a,5,6-hexahydro-1H-naphthalene[1]
Identifiers
CAS Number	334499-19-3;
3D model (JSmol)	Interactive image;
ChemSpider	8140918;
PubChem CID	9965325;
	InChI InChI=1S/C20H32/c1-14(2)7-6-8-16(4)19-12-10-17(5)18-11-9-15(3)13-20(18)19/h7,13,16-19H,3,6,8-12H2,1-2,4-5H3/t16-,17-,18+,19+/m0/s1 Key: DTMNMDQQDKQKIE-INDMIFKZSA-N;
	SMILES CC1CCC(C2=CC(=C)CCC12)C(C)CCC=C(C)C;
Properties
Chemical formula	C20H32
Molar mass	272.476 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Elisabethatriene is a bicyclic compound found in the marine octocoral Pseudopterogorgia elisabethae.[2] Its stereochemistry is identical to the stereochemistry of elisabethatrienol.[2]

References

"Elisabethatriene". PubChem Compound Database. National Center for Biotechnology Information. 14 January 2017. Archived from the original on 15 January 2017. Retrieved 15 January 2017.
Masayuki Nasuda; Miho Ohmori; Kiyoshi Ohyama; Yoshinori Fujimoto (1 May 2012). "Revision of the stereochemistry of elisabethatriene, a putative biosynthetic intermediate of pseudopterosins". Chemical and Pharmaceutical Bulletin (Tokyo). The Pharmaceutical Society of Japan. 60 (5): 681–685. PMID 22689408. Archived from the original on 15 January 2017. Retrieved 15 January 2017.

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[PubChem-1] "Elisabethatriene". PubChem Compound Database. National Center for Biotechnology Information. 14 January 2017. Archived from the original on 15 January 2017. Retrieved 15 January 2017.

[Nasuda-2] Masayuki Nasuda; Miho Ohmori; Kiyoshi Ohyama; Yoshinori Fujimoto (1 May 2012). "Revision of the stereochemistry of elisabethatriene, a putative biosynthetic intermediate of pseudopterosins". Chemical and Pharmaceutical Bulletin (Tokyo). The Pharmaceutical Society of Japan. 60 (5): 681–685. PMID 22689408. Archived from the original on 15 January 2017. Retrieved 15 January 2017.