Synthesis of the optically active form of the C-18 Cecropia [Hyalophora cecropia] juvenile hormone

Abstract Gas chromatographic determinations, bioassays, and radio labelling experiments show that the juvenile hormone in adult male Hyalophora cecropia is accumulated exclusively in the accessory sex glands. Moths do not store measurable quantities of juvenile hormone if their accessory sex glands are removed shortly after adult eclosion.

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Juvenile hormone activity of optically active ethyl 4-(2-benzylalkyloxy)benzoates inducing precocious metamorphosis

Journal of Pesticide Science ◽

10.1584/jpestics.g08-22 ◽

2008 ◽

Vol 33 (4) ◽

pp. 383-386 ◽

Cited By ~ 4

Author(s):

Norihiro Fujita ◽

Kenjiro Furuta ◽

Kiyo Ashibe ◽

Shuhei Yoshida ◽

Naotaka Yamada ◽

...

Keyword(s):

Juvenile Hormone ◽

Optically Active ◽

Hormone Activity ◽

Juvenile Hormone Activity

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Alterations in fatty acid composition during the metamorphosis of Hyalophora cecropia: Correlations with juvenile hormone titre

Journal of Insect Physiology ◽

10.1016/0022-1910(70)90218-0 ◽

1970 ◽

Vol 16 (5) ◽

pp. 851-864 ◽

Cited By ~ 21

Author(s):

William F. Stephen ◽

Lawrence I. Gilbert

Keyword(s):

Fatty Acid Composition ◽

Fatty Acid ◽

Juvenile Hormone ◽

Acid Composition ◽

Hyalophora Cecropia

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ChemInform Abstract: A New Method for Synthesis of Allenes, Including an Optically Active Form, from Aldehydes and Alkenyl Aryl Sulfoxides by Sulfoxide-Metal Exchange as the Key Reaction and an Application to a Total Synthesis of Male Bean Weevil Sex Attr

ChemInform ◽

10.1002/chin.200232069 ◽

2010 ◽

Vol 33 (32) ◽

pp. no-no

Author(s):

Tsuyoshi Satoh ◽

Noriko Hanaki ◽

Yuko Kuramochi ◽

Yujiro Inoue ◽

Kayo Hosoya ◽

...

Keyword(s):

Total Synthesis ◽

Active Form ◽

Optically Active ◽

New Method ◽

Metal Exchange ◽

Bean Weevil

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ENANTIOSPECIFIC SYNTHESIS OF (+)-ERYTHRO-(5S,6R)-6-ACETOXY-5-HEXADECANOLIDE, AN OPTICALLY ACTIVE FORM OF THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE

Chemistry Letters ◽

10.1246/cl.1983.1835 ◽

1983 ◽

Vol 12 (12) ◽

pp. 1835-1836 ◽

Cited By ~ 21

Author(s):

Yukio Masaki ◽

Kinnosuke Nagata ◽

Kenji Kaji

Keyword(s):

Active Form ◽

Optically Active ◽

Oviposition Attractant ◽

Mosquito Oviposition ◽

Attractant Pheromone ◽

Enantiospecific Synthesis

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A new method for synthesis of allenes, including an optically active form, from aldehydes and alkenyl aryl sulfoxides with carboncarbon bond-formation

Tetrahedron Letters ◽

10.1016/s0040-4039(99)01666-4 ◽

1999 ◽

Vol 40 (50) ◽

pp. 8815-8818 ◽

Cited By ~ 42

Author(s):

Tsuyoshi Satoh ◽

Yuko Kuramochi ◽

Yujiro Inoue

Keyword(s):

Bond Formation ◽

Active Form ◽

Optically Active ◽

New Method ◽

Carbon Bond ◽

Carbon Carbon Bond

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Isolation, structure, and synthesis of chenopodanol and the absolute configuration of chenopodene and chenopodanol

Canadian Journal of Chemistry ◽

10.1139/v97-077 ◽

1997 ◽

Vol 75 (6) ◽

pp. 634-640 ◽

Cited By ~ 11

Author(s):

Motoo Tori ◽

Tomonobu Hamaguchi ◽

Mamiko Aoki ◽

Masakazu Sono ◽

Yoshinori Asakawa

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Active Form ◽

Optically Active ◽

Spectroscopic Techniques ◽

The Absolute

(−)-Chenopodanol (2) has been isolated from the liverwort Marchantiachenopoda and its structure determined by spectroscopic techniques as well as by total synthesis. Chenopodene (1) has also been synthesized in an optically active form, resulting in revision of the originally assigned absolute configuration. Keywords: chenopodanol, chenopodene, liverwort, Marchantiachenopoda, sesquiterpene.

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