Výsledky vyhledávání - "I. M. Ladenkova"

Insect pheromones and their analogues XLVIII. A convenient synthesis of the 10E,12Z- and 10E,12E- isomers of hexadecadien-1-ol and of hexadeca-10E,12Z-dienal — Components of the sex pheromone of the silkworm moth

Autor: A. V. Kuchin, G. Yu. Ishmuratov, E. V. Gorobets, O. V. Sokol'skaya, I. M. Ladenkova, Tolstikov Genrikh A, Vnira R. Akhmetova, V. N. Odinokov, R. R. Muslukhov

Publikováno v: Chemistry of Natural Compounds. 29:668-673

The 10E,12Z- and 10E,12E- isomers of hexadecadien-1-ol and of hexadeca-10E,12Z-dienal — components of the sex pheromone of the silkworm mothBombyx mori — have been synthesized from the readily available octa-2E,7-dien-1-ol.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4985c6c46b603de5175cd87017927fa3
https://doi.org/10.1007/bf00630222

Zobrazit plný text záznamu

Insect pheromones and their analogues. XLV. Synthesis of mono-and dienic components of insect pheromones from isopropyl nona-3E,8-dienoate

Autor: O. V. Sokol'skaya, L. Yu. Gubaidullin, I. M. Ladenkova, R. R. Muslukhov, V. N. Odinokov, Tolstikov Genrikh A, G. Yu. Ishmuratov

Publikováno v: Chemistry of Natural Compounds. 29:123-127

Non-6E-en-l-ol, dodec-3E-en-l-yl acetate, and dodeca-7E, 9Z-dien-l-yl acetate, which are components of sex pheromomes of insects of the orderLepidoptera, have been synthesized from the readily accessible isopropyl nona-3E,8-dienoate.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6a26b66a623637ae0bc74a16662551ce
https://doi.org/10.1007/bf00631038

Zobrazit plný text záznamu

Insect pheromones and their analogues XL. Synthesis of dodec-3Z-EN-11RS-olide (ferrulactone II — A racemic analogue of a component of the aggregation pheromone of Cryptolestes ferrugineus

Autor: G. Yu. Ishmuratov, L. P. Botsman, R. R. Vakhidov, V. N. Odinokov, T. A. Kargapol'tseva, Tolstikov Genrikh A, I. M. Ladenkova

Publikováno v: Chemistry of Natural Compounds. 28:369-374

A new route, based on the partial ozonolysis of ω-acetyl derivatives of alk-1-en-4-ynes, is proposed for the synthesis of 11RS-hydroxydodec-3Z-enoic acid, the cyclization of which gives dodec-3Z-en-11RS-olide (ferrulactone II) — a racemic analogue

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0d861bd30a97effdc046667c099cfca1
https://doi.org/10.1007/bf00630261

Zobrazit plný text záznamu

Insect phermones and their analogues XXXIX. Synthesis of 11RS-hydroxy- and 12-hydroxydodec-3Z-enoic acids — Acyclic precursors of the macrolide components of the pheromones of Cryptolestes ferrugineus and C. pusillus

Autor: I. M. Ladenkova, V. N. Odinokov, R. R. Vakhidov, G. Yu. Ishmuratov, Tolstikov Genrikh A, L. P. Botsman, R. R. Khametova

Publikováno v: Chemistry of Natural Compounds. 28:365-369

A new approach to the synthesis of 11RS-hydroxy- and 12-hydroxydodec-3Z-enoic acids has been developed with the use, in one of the key stages, of the partial ozonolysis of the acetates of the corresponding methylene-separated enynic alcohols.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::75fa8754a900b18608c1124089e6ae2c
https://doi.org/10.1007/bf00630260

Zobrazit plný text záznamu

Pheromones of insects and their analogs. XXVII. Synthesis of 10-hydroxy-4,8-dimethyldeca-4E,8E-dienoic acid and of racemic 4,8-dimethyldecanal from geranyl acetate

Autor: G. Yu. Ishmuratov, R. R. Muslukhov, V. N. Odinokov, I. M. Ladenkova, Tolstikov Genrikh A

Publikováno v: Chemistry of Natural Compounds. 27:234-237

10-Hvdroxy-4,8-dimethyldeca-4E,8E-dienoic acid and racemic 4,8-dimethyldecanal (components of beetle pheromones) have been synthesized from geranyl acetate.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1430ebac279d582054237c1adbe05079
https://doi.org/10.1007/bf00629769

Zobrazit plný text záznamu

Insect pheromones and their analogues XXIV. Synthesis of long-chain 1,5-dimethyl-branched pheromones from geranyl acetate

Autor: G. Yu. Ishmuratov, Tolstikov Genrikh A, I. M. Ladenkova, V. N. Odinokov

Publikováno v: Chemistry of Natural Compounds. 26:697-701

Schemes for the synthesis of long-chain 1,5-dimethyl-branched pheromones (7,11-dimethyloctadecane, 15,19-dimethyltritriacontane, and 2-acetoxy-3,7-dimethylpentadecane) from the product of the allyl oxidation of geranyl acetate (8-acetoxy-2,6-dimethyl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0b3b339cc36c95ef8a0ba9e9051f7e49
https://doi.org/10.1007/bf00630084

Zobrazit plný text záznamu

Pheromones of insects and their analogs

Autor: I. M. Ladenkova, T. A. Kargapol'tseva, L. P. Botsman, Tolstikov Genrikh A, G. Yu. Ishmuratov, V. N. Odinokov

Publikováno v: Chemistry of Natural Compounds. 27:621-623

From cyclohexene and caproaldehyde, using ozonolysis and the Knoevenagel reaction, we have synthesized hexadeca-7Z,11E-dien-l-yl acetate — the sex pheromone ofSitotroga cerealella and a component of the sex pheromone ofPectinophora gossypiella.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c341f3718ddb362b19a61cc0e48f8621
https://doi.org/10.1007/bf00630368

Zobrazit plný text záznamu

Pheromones of insects and their analogs. XXVIII. Practical synthesis of tetradeca-9Z,12E-dien-1-yl acetate ? A component of the sex pheromones of insects of the order lepidoptera

Autor: Tolstikov Genrikh A, Usein M. Dzhemilev, L. P. Botsman, I. M. Ladenkova, V. N. Odinokov, G. Yu. Ishumuratov, T. A. Kargapol'teva, A. P. Zolotarev, Askhat G. Ibragimov

Publikováno v: Chemistry of Natural Compounds. 27:238-240

Tetradeca-9Z,12E-dien-l-yl acetate, a sex pheromone of the Indian meal mothPlodia interpunctella has been synthesized from the readily available product of the hydrodimerization of butadiene — octa-1,7-diene.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9f036da32ad95282e745fc57b999cad7
https://doi.org/10.1007/bf00629770

Zobrazit plný text záznamu

Insect pheromones and their analogues XXV. Synthesis of acetylenic precursors of pheromones from undecylenic acid

Autor: V. N. Odinokov, Tolstikov Genrikh A, G. Yu. Ishmuratov, I. M. Ladenkova, E. M. Vyrypaev

Publikováno v: Chemistry of Natural Compounds. 26:702-704

The selective ozonolysis of pentadec-1-en-12-yne and heptadec-1-en-12-yne, synthesized from the readily available undecylenic acid, has given tetradec- and hexadec-11-yn-1-ols — acetylenic precursors of a number of pheromones of insects of the orde

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1f61d11daf8262a34d8c7801d1169be4
https://doi.org/10.1007/bf00630085

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání