Výsledky vyhledávání - "Shin-Etsu Muto"

Akademický článek

Autor: Nobuyuki Endo, Tetsuya Yasuda, Takashi Wada, Shin-etsu Muto, Rikiya Sasaki

Publikováno v: Psyche: A Journal of Entomology, Vol 2012 (2012)

Males of the Piezodorus hybneri stink bug produce a pheromone comprising β-sesquiphellandrene (Sesq), (R)-15-hexadecanolide (R15), and methyl (Z)-8-hexadecenoate (Z8). We collected airborne volatiles from individual P. hybneri males and analyzed the

Externí odkaz: https://doaj.org/article/1d33a3219f474c6fad51aecf0422f8f3

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Possible function of Piezodorus hybneri (Heteroptera: Pentatomidae) male pheromone: Effects of adult age and diapause on sexual maturity and pheromone production

Autor: Shin-etsu Muto, Rikiya Sasaki, Nobuyuki Endo, Tetsuya Yasuda, Takashi Wada, Keiichiro Matsukur

Publikováno v: Applied Entomology and Zoology. 42:637-641

To estimate the biological function of the male-produced pheromone of Piezodorus hybneri, we investigated the relationship between sexual maturity and pheromone production. Copulation was first observed at day 4 after emergence of males. The males sh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3f751827b8fde121fafdd1944f70e2c7
https://doi.org/10.1303/aez.2007.637

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Synthesis and Stereochemistry of the Four Himachalene-Type Sesquiterpenes Isolated from the Flea Beetle (Aphthona flava) as Pheromone Candidates

Autor: Kenji Mori, Shin-etsu Muto, Masahiko Bando

Publikováno v: European Journal of Organic Chemistry. 2004:1946-1952

Both the (1S,2R) and (1R,2S) isomers of 2,6,6-trimethylbicyclo[5.4.0]undec-7-en-9-one (1) were synthesized by starting from (S)- and (R)-citronellal (5), respectively. The stereochemistry of (1R,2S)-(−)-1 was established by an X-ray analysis; it ex

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eb6f0543a9eedb6f193dc1c99cb3d577
https://doi.org/10.1002/ejoc.200300812

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Synthesis of all Four Stereoisomers of Leucomalure, Components of the Female Sex Pheromone of the Satin Moth, Leucoma salicis

Autor: Shin-etsu Muto, Kenji Mori

Publikováno v: European Journal of Organic Chemistry. 2003:1300-1307

Lipase PS-C(Amano)-catalyzed asymmetric acetylation of (±)-4-(tert-butyldiphenylsilyloxy)-cis-2,3-epoxy-1-butanol afforded the (2R,3S)-epoxy alcohol and the (2S,3R)-epoxyacetate, which were converted into all of the four stereoisomers of leucomalure

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::102e0c58944b2ac63939a1c8e985acc9
https://doi.org/10.1002/ejoc.200390186

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Synthesis of Germacrene-B and Its Extension to the Synthesis of (±)-9-Methylgermacrene-B, the Racemate of the Male-Produced Sex Pheromone of the SandflyLutzomyia longipalpis from Lapinha, Brazil

Autor: Shin-etsu Muto, Yutaka Nishimura, Kenji Mori

Publikováno v: European Journal of Organic Chemistry. 1999:2159-2165

Both germacrene-B (2) and 9-methylgermacrene-B [(±)-1] were synthesized by employing cyclization reactions [8 9 and (±)-20 (±)-21] as the key steps. The latter [(±)-1] was shown to be the racemate of the male-produced sex pheromone of the sandfly

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3c8ff9325677fa60df58d549d84ab5ed
https://doi.org/10.1002/(sici)1099-0690(199909)1999:9<2159::aid-ejoc2159>3.0.co

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Synthesis of sphingosine relatives. Part 22. Synthesis of sulfobacin A, B and flavocristamide A, new sulfonolipids isolated from Chryseobacterium sp

Autor: Shin‐etsu Muto, Akihiro Kayo, Kenji Mori, Hirosato Takikawa, Dai Nozawa

Publikováno v: Journal of the Chemical Society, Perkin Transactions 1. :2467-2477

Sulfobacin A (1), B (2), and flavocristamide A (3), new sulfonolipids isolated from Chryseobacterium sp. were synthesized stereoselectively by starting from L-cysteine.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::363f6c8b68cc877099ed0f2f0b8a23de
https://doi.org/10.1039/a904258j

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Synthesis of sulfobacin A and B, new sulfonolipids isolated from Chryseobacterium sp

Autor: Shin‐etsu Muto, Dai Nozawa, Hirosato Takikawa, Akihiro Kayo, Kenji Mori

Publikováno v: Tetrahedron Letters. 39:6931-6934

Sulfobacin A (1) and B (2), new sulfonolipids isolated from Chryseobacterium sp. as von Willebrand factor antagonists, were synthesized stereoselectively by starting from l-cysteine.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8d2b61e0fd4dedaf9b36707904b78e4f
https://doi.org/10.1016/s0040-4039(98)01456-7

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Diastereoselective epoxidation of the double bond at C-4 of sphingosines to provide phytosphingosine relatives such as α-galactosylceramide KRN7000

Autor: Shin-etsu Muto, Hirosato Takikawa, Kenji Mori

Publikováno v: Tetrahedron. 54:3141-3150

Diastereoselective epoxidation of the double bond at C-4 of two sphingosine derivatives [3, R = (CH2)7Me or (CH2)12Me] was studied. Dimethyldioxirane was found to be the best oxidant for that purpose. Application of this epoxidation resulted in a new

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1ec5a3ff7ad8866f69ce3a4385dc6cbb
https://doi.org/10.1016/s0040-4020(98)00065-9

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ChemInform Abstract: Synthesis of Sulfobacin A and B, New Sulfonolipids Isolated from Chryseobacterium sp

Autor: Kenji Mori, Hirosato Takikawa, Dai Nozawa, Akihiro Kayo, Shin‐etsu Muto

Publikováno v: ChemInform. 29

Sulfobacin A (1) and B (2), new sulfonolipids isolated from Chryseobacterium sp. as von Willebrand factor antagonists, were synthesized stereoselectively by starting from l-cysteine.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c9eef9e71e0900ff3b4f4422552c5f34
https://doi.org/10.1002/chin.199849294

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