31502-21-3Relevant articles and documents
Synthesis of 5Z,9E-tridecadien-1-ylacetate, an attractant of Trichoplusia ni
Vakhidov,Alekseev
, p. 94 - 95 (2011)
A new synthetic scheme for 5Z,9E-tridecadien-1-ylacetate, an attractant of the cabbage looper Trichoplusia ni (Huebner) was developed using a highly stereoselective Claisen rearrangement.
Total synthesis of gibbilimbols A-D
Vyvyan, James R.,Holst, Christian L.,Johnson, Allison J.,Schwenk, Cheryl M.
, p. 2263 - 2265 (2007/10/03)
Gibbilimbols A-D (1-4) were synthesized in 32-49% yield over four steps from commercially available starting materials. A copper-catalyzed coupling of 4-methoxyphenylmagnesium bromide with various unsaturated alkyl bromides was the key step in assembling the (long-chain alkyl)-phenol skeleton.
Synthesis of batzelladine E and its E isomer
Snider, Barry B.,Chen, Jinsheng
, p. 5697 - 5700 (2007/10/03)
The synthesis of 4E established that batzelladine E (4Z) has the Z- rather than the E-stereochemistry previously depicted. Batzelladine E (4Z) has been synthesized by an efficient 9-step route in 3% overall yield.
COMPOUNDS WITH A HERBAL ODOR VI. THE E ISOMERS OF THE STRUCTURAL ANALOGS OF LEAF ALCOHOL
Vasil'ev, A. A.,Cherkaev, G. V.,Nikitina, M. A.
, p. 870 - 875 (2007/10/02)
The E isomers of leaf alcohol and its structural analogs differing in the length of the carbon chain, the presence of substituents at various positions of the molecule, the position of the double bond, and replacement of the double bond by a three-membered ring were synthesized.Many representatives of the Z and E series have a herbal odor, and similarity is observed in the odor of the respective pairs of Z and E isomers.The proximity of the odor of the investigated compounds to the standard (leaf alcohol) is determined by the number of carbon atoms in their molecules.
