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3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil

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3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil. / Hamilton, J. Gordon C.; Hooper, Antony M.; Mori, Kenji et al.
In: Chemical Communications, No. 4, 21.02.1999, p. 355-356.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Hamilton, JGC, Hooper, AM, Mori, K, Pickett, JA & Sano, S 1999, '3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil', Chemical Communications, no. 4, pp. 355-356. https://doi.org/10.1039/a900242a

APA

Hamilton, J. G. C., Hooper, A. M., Mori, K., Pickett, J. A., & Sano, S. (1999). 3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil. Chemical Communications, (4), 355-356. https://doi.org/10.1039/a900242a

Vancouver

Hamilton JGC, Hooper AM, Mori K, Pickett JA, Sano S. 3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil. Chemical Communications. 1999 Feb 21;(4):355-356. doi: 10.1039/a900242a

Author

Hamilton, J. Gordon C. ; Hooper, Antony M. ; Mori, Kenji et al. / 3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil. In: Chemical Communications. 1999 ; No. 4. pp. 355-356.

Bibtex

@article{399285a8d861482aa057406914e112fa,
title = "3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil",
abstract = "The structure of the sex pheromone produced by the male sandfly Lutzomyia longipalpis, from the Jacobina region of Brazil, previously proposed tentatively as the novel homosesquiterpene 3-methyl-α-himachalene is confirmed by synthesis and biological activity; the relative stereochemistry is defined as 1RS,3RS,7RS by comparing the natural product with the four synthetic diastereoisomers.",
author = "Hamilton, {J. Gordon C.} and Hooper, {Antony M.} and Kenji Mori and Pickett, {John A.} and Satoshi Sano",
year = "1999",
month = feb,
day = "21",
doi = "10.1039/a900242a",
language = "English",
pages = "355--356",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "4",

}

RIS

TY - JOUR

T1 - 3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil

AU - Hamilton, J. Gordon C.

AU - Hooper, Antony M.

AU - Mori, Kenji

AU - Pickett, John A.

AU - Sano, Satoshi

PY - 1999/2/21

Y1 - 1999/2/21

N2 - The structure of the sex pheromone produced by the male sandfly Lutzomyia longipalpis, from the Jacobina region of Brazil, previously proposed tentatively as the novel homosesquiterpene 3-methyl-α-himachalene is confirmed by synthesis and biological activity; the relative stereochemistry is defined as 1RS,3RS,7RS by comparing the natural product with the four synthetic diastereoisomers.

AB - The structure of the sex pheromone produced by the male sandfly Lutzomyia longipalpis, from the Jacobina region of Brazil, previously proposed tentatively as the novel homosesquiterpene 3-methyl-α-himachalene is confirmed by synthesis and biological activity; the relative stereochemistry is defined as 1RS,3RS,7RS by comparing the natural product with the four synthetic diastereoisomers.

U2 - 10.1039/a900242a

DO - 10.1039/a900242a

M3 - Journal article

AN - SCOPUS:0033590698

SP - 355

EP - 356

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 4

ER -