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Cis Jasmone

http://amcrasto.wix.com/anthony-melvin-crasto/apps/blog/cis-jasmone
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Jasmone is a natural organic compound extracted from the volatile portion of the oil fromjasmine flowers. It is a colorless to pale yellow liquid that has the odor of jasmine. Jasmone can exist in two isomeric forms with differing geometry around the pentenyl double bond, cis-jasmone and trans-jasmone. The natural extract contains only the cis form, while synthetic material is often a mixture containing both forms, with the cis form predominating. Both forms have similar odors and chemical properties.

Jasmone is produced within plants by the metabolism of jasmonate, from linolenic acid by the octadecanoid pathway. It can act as either an attractant or a repellent for various insects. Commercially jasmone is used primarily in perfumes and cosmetics.

An attempt to make Z jasmone – an important constituent of many perfumes

In fact one synthesis uses the following as carbon sources:

cis (Z) jasmone ,

cas no 488-10-8, 3-methyl-2-[(2Z)-pent-2-en-1-yl]cyclopent-2-en-1-one

ref-(Can. J. Chem. 1978, Vol 56, p2301)

1    W. Theilheimer. Synthetic Methods of Organic Chemistry. Volume 31, 1977, p. 352 
2   Tetrahedron, 39 (24), p. 4127, 1983

Thomas Koch, Katja Bandemer, Wilhelm Boland (1997). "Biosynthesis of cis-Jasmone: a pathway for the inactivation and the disposal of the plant stress hormone jasmonic acid to the gas phase?". Helvetica Chimica Acta 80 (3): 838–850.doi:10.1002/hlca.19970800318.

Predict NMR spectrum

Formula: C10H14O
CAS#: 488-10-8
MW: 150.22






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A New Bidesmoside Saponin from the Bark of Guaiacum officinale

June 15, 2012

A new bidesmosidic triterpene saponin, guaianin P was isolated from the stem bark of
Guaiacum officinale. Its structure was established as oleanolic acid 3-O-{α-L-rhamnopyranosyl-
(1→3)-α-L-rhamnopyranosyl-(1→2)-[β-D-glucopyranosyl-(1→3)]-α-L-arabinopyranoside}-28-O-
β-D-glucopyranosyl ester by spectroscopic and chemical

http://jcsp.org.pk/index.php/jcsp/article/viewFile/4177/2961  is the link
J. Chem.Soc.Pak., Vol. 34, No. 2, 2012 BY
NIKHAT SABA et al.,
RASHEEDA KHATOON, ZULFIQAR ALI and VIQAR UDDIN AHMAD
KARACHI
Guaianin P  is very nicely described
https://docs.google.com/viewer?url=http%3A%2F%2Fprr.hec.gov.pk%2FChapters%2F612-0.pdf
Above link gives the structures


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ANTHONY MELVIN CRASTO
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NICE PAPER IN A PAKISTANI JOUNAL

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