Literature DB >> 24248506

Propheromones derived from codlemone.

L Streinz1, A Horák, J Vrkoč, I Hrdý.   

Abstract

Tricarbonyl [(8,9,10,11-η-8,10-dodecadien-l-ol] iron and the corresponding acetate prepared from 8,10-dodecadien-1-ol or its acetate, comprise the protected double-bond system of the molecule. After coming in contact with ambient oxygen, the iron complexes in question slowly release the corresponding pheromones of, for example, the codling moth,Cydia pomonella, and the pea moth,Cydia nigricana in highE,E purity and amounts that are sufficient for pest monitoring. A simple dispenser for propheromone application is proposed. Results of release rates in laboratory conditions and field trials are given.

Entities:  

Year:  1993        PMID: 24248506     DOI: 10.1007/BF00987466

Source DB:  PubMed          Journal:  J Chem Ecol        ISSN: 0098-0331            Impact factor:   2.626


  8 in total

1.  Trimerization ofEarias insulana sex pheromone, (E,E)-10,12-Hexadecadienal, A phenomenon affecting trapping efficiency.

Authors:  E Dunkelblum; M Kehat; J T Klug; A Shani
Journal:  J Chem Ecol       Date:  1984-03       Impact factor: 2.626

2.  Insect sex pheromones: Determination of half-lives from formulations by collection of emitted vapor.

Authors:  L M McDonough; L I Butler
Journal:  J Chem Ecol       Date:  1983-11       Impact factor: 2.626

3.  Sex pheromone of European grapevine moth (Lobesia botrana) its chemical transformations in sunlight and heat.

Authors:  R Ideses; A Shani; J T Klug
Journal:  J Chem Ecol       Date:  1982-06       Impact factor: 2.626

4.  Sex pheromone of the pea moth,Cydia nigricana (F.) (Lepidoptera: Olethreutidae).

Authors:  A R Greenway
Journal:  J Chem Ecol       Date:  1984-07       Impact factor: 2.626

5.  Propheromones that release pheromonal carbonyl compounds in light.

Authors:  X Liu; E D Macaulay; J A Pickett
Journal:  J Chem Ecol       Date:  1984-05       Impact factor: 2.626

6.  Sex pheromone of Egyptian cotton leafworm (Spodoptera littoralis). Its chemical transformation under field conditions.

Authors:  A Shani; J T Klug
Journal:  J Chem Ecol       Date:  1981-07       Impact factor: 2.626

7.  Attractant lures for males of the pea moth,Cydia nigricana (F.) Containing (E)-10-dodecen-1-yl acetate and (E,E)-8,10-dodecadien-1-yl acetate.

Authors:  A R Greenway; C Wall
Journal:  J Chem Ecol       Date:  1981-05       Impact factor: 2.626

8.  Rubber substrates and their influence on isomerization of conjugated dienes in pheromone dispensers.

Authors:  J Vrkoč; K Konečný; I Valterová; I Hrdý
Journal:  J Chem Ecol       Date:  1988-05       Impact factor: 2.626

  8 in total
  3 in total

1.  Behavioral observations and measurements of aerial pheromone in a mating disruption trial against pea mothCydia nigricana F. (Lepidoptera, Tortricidae).

Authors:  P Witzgall; M Bengtsson; G Karg; A C Bäckman; L Streinz; P A Kirsch; Z Blum; J Löfqvist
Journal:  J Chem Ecol       Date:  1996-02       Impact factor: 2.626

2.  Sustained production of the labile pheromone component, (Z,Z)-6,9-heneicosadien-11-one, from a stable precursor for monitoring the whitemarked tussock moth.

Authors:  Gary G Grant; Wei Liu; Keith N Slessor; Mamdouh M Abou-Zaid
Journal:  J Chem Ecol       Date:  2006-08-03       Impact factor: 2.626

3.  Sex pheromone of horse-chestnut leafminer Camneraria ohridella and its use in a pheromone-based monitoring system.

Authors:  B Kalinová; A Svatos; J Kindl; O Hovorka; I Hrdý; J Kuldová; M Hoskovec
Journal:  J Chem Ecol       Date:  2003-02       Impact factor: 2.626

  3 in total

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