Jump to content

Elisabethatriene

From Wikipedia, the free encyclopedia
Elisabethatriene
Names
Preferred IUPAC name
(1R,4S,4aR)-4-Methyl-1-[(2S)-6-methylhept-5-en-2-yl]-7-methylidene-1,2,3,4,4a,5,6,7-octahydronapthalene
Identifiers
3D model (JSmol)
ChemSpider
  • 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
  • CC1CCC(C2=CC(=C)CCC12)C(C)CCC=C(C)C
Properties
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).

Elisabethatriene is a bicyclic compound found in the marine octocoral Pseudopterogorgia elisabethae.[1] Its stereochemistry is identical to the stereochemistry of elisabethatrienol.[1]

References

[edit]
  1. ^ a b 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. 60 (5). The Pharmaceutical Society of Japan: 681–685. doi:10.1248/cpb.60.681. PMID 22689408. Archived from the original on 15 January 2017. Retrieved 15 January 2017.