© Benaki Phytopathological Institute
Mihou & Michaelakis
54
mosquito oviposition pheromone and highly
fluorinated analog retaining biological activity.
Journal of Chemical Ecology
, 16: 1779-1789.
Dhotare, B., Goswami, D. and Chattopadhyay, A.
2005. (
R
)-2,3-Cyclohexylideneglyceraldehyde, a
novel template for stereoselective preparation
of functionalized
δ
-lactones: Synthesis of mos-
quito oviposition pheromone.
Tetrahedron Let-
ters
, 46: 6219-6221.
Gallos, J.K., Mihelakis, D.S., Dellios, C.C. and Poza-
rentzi, M.E. 2000. A new synthesis of (–)-(5
R
,6
S
)
-6-acetoxy-5-hexadecanolide. The mosqui-
to
Culex pipiens
fatigans oviposition attractant
pheromone.
Heterocycles
, 53: 703-707.
Gravier-Pelletier, C., Sanière, M., Charvet, I., LeMerrer,
Y. and Depezay, J.C. 1994. Synthesis of (–)-muri-
catacin and (–)-(5
R
,6
S
)-6-acetoxy-5-hexadecan-
olide, the mosquito oviposition attractant phe-
romone, from
D
-isoascorbic acid.
Tetrahedron
Letters
, 35(1): 115-118.
Henkel, B., Kunath, A. and Schick, H. 1995. Chemo-
enzymatic synthesis of (5
R
,6
S
)-6-acetoxyhex-
adecan-5-olide – The major component of the
mosquito oviposition attractant pheromone.
Liebigs Annalen
, 921-923.
Hwang, Y.S., Mulla, M.S., Chaney, J.D., Lin, G.G. and
Xu, H.J. 1987. Attractancy and species specific-
ity of 6-Acetoxy-5-hexadecanolide, a mosqui-
to oviposition attractant pheromone.
Journal of
Chemical Ecology
, 13: 245-252.
Ichimoto, I., Yoshizawa, T., Machiya, K., Kirihata, M.,
and Ueda, H. 1988. An efficient synthesis of
mosquito oviposition attractant pheromone,
(5
R
,6
S
)-(–)-6-acetoxy-5-hexadecanolide.
Chem-
istry Express
, 11: 687-690.
Iltis, W.G. and Zweig, G. 1962. Surfactant in apical
drop of eggs of some
culicine
mosquitoes. An-
nals of the
Entomological Society of America
, 55:
409-415.
Ikishima, H., Sekiguchi, Y., Ichikawa, Y. and Kotsuki,
H. 2006. Synthesis of (–)-(5
R
,6
S
)-6-acetoxyhexa-
decanolide based on
L
-proline-catalyzed asym-
metric aldol reactions.
Tetrahedron
, 62: 311-316.
Kametani, T., Tsubuki, M., Tatsuzaki, Y. and Honda, T.
1990. Synthesis of optically active 2-furylmeth-
anols as useful chiral building blocks and its appli-
cation to the synthesis of (5
R
,6
S
)-6-acetoxyhexa-
decan-5-olide and (+)-disparlure.
Journal of The
Chemical Society-Perkin Transactions 1
: 639-646.
Kang, S.K., and Cho, I.H. 1989. An enantiospecific
synthesis of (–)-(5
R
,6
S
)-6-acetoxy-5-hexadecan-
olide, the mosquito oviposition attractant phe-
romone.
Tetrahedron Letters
, 30: 743-746.
Ko, K.Y., and Eliel, E.L.. 1986. Asymmetric synthesis
of (5
R
,6
S
)-6-acetoxy-hexadecanolide, the major
component of the oviposition attractant phe-
romone of the mosquito
Culex pipiens fatigans
,
and two of its stereoisomers.
Journal of Organic
Chemistry
, 51: 5353-5362.
Kotsuki, H., Kadota, I., and Ochi, M. 1990. A novel car-
bon-carbon bond-forming reaction of triflates
with copper(I)-catalysed Grignard reagents. A
new concise and enantiospecific synthesis of
(+)-exo-Brevicomin,
(5
R
,6
S
)-(–)-6-acetoxy-5-
hexadecanolide and
L
-Factor.
Journal of Organ-
ic Chemistry
, 55: 4417-4422.
Kioulos, E., Koliopoulos, G., Couladouros, E. A., and
Michaelakis, A. 2007-2008. Laboratory evalua-
tion of three larvicides and preliminary studies
of the attract–and–kill strategy on hatched lar-
vae of
Culex pipiens
(Diptera: Culicidae)
. Entomo-
logia Hellenica
, 17: 3-11.
Laurence, B.R., and Pickett, J.A. 1982.
Erythro-6-ac-
etoxy-5-hexadecanolide, the major component
of an oviposition attractant pheromone.
Jour-
nal of the Chemical Society, Chemical Communi-
cations
, 1: 59-60.
Laurence, B.R., and Pickett, J.A. 1985. An oviposition
attractant pheromone in
Culex quinquefasciatus
Say (Diptera: Culicidae).
Bulletin of Entomological
Research
, 75: 283-290.
Leal, W.S., Barbosa, M.R., Xu, W., Ishida, Y., Syed, Z.,
Latte, N., Chen, M.A., Morgan, T.I., Cornel, J.A.,
and Furtado, A. 2008. Reverse and conventional
chemical ecology approaches for the develop-
ment of ovipositor attractants for
Culex
mosqui-
toes.
PLoS ONE
, 3:1-11
Lin G.Q., Xu H.J., Wu B.C., Guo G.Z., and Zhou, W.S.
1985. Studies on the identification and synthe-
ses of insect pheromones. Stereoselective syn-
thesis of all the possible optical isomers of the
mosquito oviposition attractant pheromone.
Tetrahedron Letters
, 26: 1233-1236.
Lohray, B.B., and Venkateswarlu, S. 1997. Intramolec-
ular
S
N
2
ring opening of a cyclic sulfate: synthe-
sis of erythro-(–)-6-acetoxy-5-hexadecanolide a
major component of mosquito oviposition at-
tractant pheromone.
Tetrahedron Asymmetry
, 8:
633-638.
Machiya, K., Ichimoto, I., Kirihata, M., and Ueda, H.
1985. A convenient synthesis of four stereoi-
somers of 6-acetoxy-5-hexadecanolide, the ma-
jor component of the mosquito oviposition at-
tractant pheromone.
Agricultural and Biological
Chemistry,
49: 643-649.
Mboera, L.E.G., Mdira, K.Y., Salum, F.M., Takken, W.,
and Pickett, J.A. 1999. Influence of synthetic ovi-
position pheromone and volatiles from soakage
pits and grass infusions upon oviposition site se-
lection of
Culex
mosquitoes in Tanzania.
Journal
of Chemical Ecology
, 25: 1855-1865.
Michaelakis, A., Mihou, A.P., Koliopoulos, G. and Cou-
ladouros, E.A. 2009. Influence of the microen-
capsulated pheromone from aged infusion as
an oviposition medium of the West Nile virus
vector
Culex pipiens
.
Parasitology Research
, 104:
1005-1009.
Michaelakis, A., Mihou, P.A., Koliopoulos, G. and Cou-
1...,14,15,16,17,18,19,20,21,22,23 25,26,27,28,29,30,31,32,33,34,...59