Zobrazeno 1 - 10 of 27 pro vyhledávání: '"Invictolide"'
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Akademický článek
Stereoselective total synthesis of some insect pheromones: (±)-serricornine and (±)-invictolide
Autor: R. A. Pilli, M. M. Murta
Publikováno v: Memorias do Instituto Oswaldo Cruz, Vol 86, Pp 117-120 (1991)
An efficient (12 steps, 12% overallyield) and stereoselective total synthesis of (±)-serricornine (1) the sex pheromone of the cigarette beetle (Lasioderma serricornine F) is described. The preparation of intermediate 5, which encompasses the proper
Externí odkaz: https://doaj.org/article/bf7268e89ffe4e908ba28351968004b8
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2
Total Synthesis of (-)-Invictolide
Autor: Ahmad Al Khazim Al Ghamdi, Attaluri R. Prasad, N. Mallikarjuna Reddy, Jhillu S. Yadav, K. Anantha Lakshmi
Publikováno v: Synthesis. 44:2595-2600
A convergent approach to the total synthesis of (–)-invictolide, a component of the queen recognition pheromone of Solenopsis­ invicta, is described. Key steps involve the desymmetrization of a bicyclic olefin with Brown’s chiral hydroboration,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::29d7bba1c33b45459707c7160e12ae05
https://doi.org/10.1055/s-0032-1316561
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3
Stereoselective total synthesis of some insect pheromones: (±)-serricornine and (±)-invictolide
Autor: Ronaldo A. Pilli, M. M. Murta
Publikováno v: Memórias do Instituto Oswaldo Cruz, Volume: 86 Supplement 2, Pages: 117-120, Published: 1991
Memórias do Instituto Oswaldo Cruz., Vol 86, Pp 117-120 (1991)
An efficient (12 steps, 12% overallyield) and stereoselective total synthesis of (±)-serricornine (1) the sex pheromone of the cigarette beetle (Lasioderma serricornine F) is described. The preparation of intermediate 5, which encompasses the proper
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8278562c4119f2b437c8e56102501bb9
https://doi.org/10.1590/s0074-02761991000600027
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4
Asymmetrische Synthese von Synargentolid A und Studien zur Synthese von Invictolid sowie Ieodomycin A und B
Autor: Reichenbach, Linus Friedemann
Publikováno v: Aachen : Publikationsserver der RWTH Aachen University 145 S. : Ill. (2014). = Aachen, Techn. Hochsch., Diss., 2014
The goal of this thesis was the asymmetric synthesis of natural products. These were Synargentoide A, Invictolide and the Ieodomycins A and B. The SAMP/RAMP methodology was used to create two or three of the streogenic centers in each of those molecu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______791::ebf1cabac3739e82087ed15f336123b0
https://publications.rwth-aachen.de/record/459455
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5
A concise enantiospecific synthesis of (−)-invictolide
Autor: Toshio Honda, Miho Katoh, Shin-ichi Yamane, Fumihiro Ishikawa
Publikováno v: Tetrahedron. 52:12177-12184
(−)-Invictolide, a component of the queen recognition pheromone of Solenopsis invicta, was stereoselectively synthesized starting from (−)-carvone, where the regioselective carbon-carbon bond cleavage reaction of γ-halo ester with samarium diiod
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c93517c659c835417de58aa15a689991
https://doi.org/10.1016/0040-4020(96)00721-1
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7
3,6,7-Tri-epi-invictolide, a diastereomer of queen recognition pheromone, and its analog from a marine-derived actinomycete
Autor: Shoichi Yamada, Seizo Sato, Hiroyuki Kawahara, Fumie Iwata
Publikováno v: The Journal of antibiotics. 64(5)
3,6,7-tri -epi -invictolide, a diastereomer of queen recognition pheromone, and its analog from a marine-derived actinomycete
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c696d8b98bb4288de34901c7d7a2859b
https://pubmed.ncbi.nlm.nih.gov/21326250
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9
ChemInform Abstract: A Concise Enantiospecific Synthesis of (-)-Invictolide
Autor: Shin-ichi Yamane, Miho Katoh, Toshio Honda, Fumihiro Ishikawa
Publikováno v: ChemInform. 28
(−)-Invictolide, a component of the queen recognition pheromone of Solenopsis invicta, was stereoselectively synthesized starting from (−)-carvone, where the regioselective carbon-carbon bond cleavage reaction of γ-halo ester with samarium diiod
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5feada9a9f1580ed910bf633129fd962
https://doi.org/10.1002/chin.199705303
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10
Synthesis of (±)-Epiinvictolide
Autor: Shinji Tanimori, Mitsuru Nakayama
Publikováno v: Agricultural and Biological Chemistry. 54:775-778
(±)-1′-Epiinvictolide [(3RS,5RS,6SR,1′SR)-3,5-dimethyl-6-(1′-methylbutyl)-tetrahydro-2H-pyran-2-one] was synthesized in 11 steps from methyl 2-oxo-6-exo-methylbicyclo[3.1.0]hexane-1-carboxylate, using a cuprous iodide-mediated homoconjugate ad
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::113e2f2ab75a879a70676cb7b2c9abaa
https://doi.org/10.1080/00021369.1990.10869992
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