Revision as of 13:30, 8 December 2010 editNono64 (talk | contribs)Autopatrolled, Pending changes reviewers, Rollbackers96,246 editsm Forsythia suspensa← Previous edit | Revision as of 13:35, 8 December 2010 edit undoNono64 (talk | contribs)Autopatrolled, Pending changes reviewers, Rollbackers96,246 editsm in caterpillarNext edit → | ||
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'''Pinoresinol''' is a ] found in ''] sp.''<ref>Pastrorova ''et al.'' (1997)</ref> or in '']''.<ref>On the stereoselective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, ]. Laurence B. Davin, Diana L. Bedgar, Takeshi Katayama and Norman G. Lewis, Phytochemistry, Volume 31, Issue 11, 1992, Pages 3869-3874, {{doi|10.1016/S0031-9422(00)97544-7}}</ref> | '''Pinoresinol''' is a ] found in ''] sp.''<ref>Pastrorova ''et al.'' (1997)</ref> or in '']''.<ref>On the stereoselective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, ]. Laurence B. Davin, Diana L. Bedgar, Takeshi Katayama and Norman G. Lewis, Phytochemistry, Volume 31, Issue 11, 1992, Pages 3869-3874, {{doi|10.1016/S0031-9422(00)97544-7}}</ref> It is also found in the caterpillar of the cabbage butterfly, '']'' where it serves as a defence against ants.<ref>Pinoresinol: A lignol of plant origin serving for defense in a caterpillar. Frank C. Schroeder, Marta L. del Campo, Jacqualine B. Grant, Douglas B. Weibel, Scott R. Smedley, Kelly L. Bolton, Jerrold Meinwald and Thomas Eisner, PNAS October 17, 2006 vol. 103 no. 42 15497-15501, {{doi|10.1073/pnas.0605921103}}</ref> | ||
==References== | ==References== |
Revision as of 13:35, 8 December 2010
Names | |
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IUPAC name 4-furan-3-yl]-2-methoxyphenol | |
Other names (+)-Pinoresinol | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
PubChem CID | |
CompTox Dashboard (EPA) | |
SMILES
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Properties | |
Chemical formula | C20H22O6 |
Molar mass | 358.38 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Pinoresinol is a lignan found in Styrax sp. or in Forsythia suspensa. It is also found in the caterpillar of the cabbage butterfly, Pieris rapae where it serves as a defence against ants.
References
- Pastrorova et al. (1997)
- On the stereoselective synthesis of (+)-pinoresinol in Forsythia suspensa from its achiral precursor, coniferyl alcohol. Laurence B. Davin, Diana L. Bedgar, Takeshi Katayama and Norman G. Lewis, Phytochemistry, Volume 31, Issue 11, 1992, Pages 3869-3874, doi:10.1016/S0031-9422(00)97544-7
- Pinoresinol: A lignol of plant origin serving for defense in a caterpillar. Frank C. Schroeder, Marta L. del Campo, Jacqualine B. Grant, Douglas B. Weibel, Scott R. Smedley, Kelly L. Bolton, Jerrold Meinwald and Thomas Eisner, PNAS October 17, 2006 vol. 103 no. 42 15497-15501, doi:10.1073/pnas.0605921103
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