Title:
OCTADIENYL ETHERS AND A PROCESS FOR MAKING OCTADIENYL ETHERS
Document Type and Number:
WIPO Patent Application WO1990013531
Kind Code:
A3
Inventors:
GRUBER BERT (DE)
WEESE KENNETH J (DE)
HOAGLAND STEVEN M (DE)
MUELLER HANS-PETER (DE)
HILL KARLHEINZ (DE)
BEHR ARNO (DE)
WEESE KENNETH J (DE)
HOAGLAND STEVEN M (DE)
MUELLER HANS-PETER (DE)
HILL KARLHEINZ (DE)
BEHR ARNO (DE)
Application Number:
PCT/US1990/002463
Publication Date:
February 06, 1992
Filing Date:
May 03, 1990
Export Citation:
Assignee:
HENKEL RESEARCH CORP (US)
International Classes:
C07C41/06; C07C43/15; C07C43/178; C07C43/215; C07C45/71; C07C47/575; C07C59/60; C07C59/68; C07H15/10; (IPC1-7): C07C43/178; C07C41/06; C07C43/15; C07C43/215; C07C47/575; C07C59/60; C07C65/28; C07C69/606; C07C69/92; C07H15/10
Foreign References:
| US4006192A | 1977-02-01 | |||
| US3530187A | 1970-09-22 |
Other References:
Journal of Medicinal Chemistry, vol. 31, no. 1, January 1988, American Chem. Soc. US; H. Nakai et al.: "New potent antagonists of leukotrienes C4 and D4. 1. Synthesis and structure-activity relationships", pages 84-91, see page 87, compound 17d and page 89, column 2
Journal of Organometallic Chemistry, vol. 137, no. 3, 20 September 1977, Elsevier Sequoia S.A. Lausanne, R. Klüter et al.: "Die Cooligomerisierung von Butadien mit alpha-Hydroxycarbonsäureestern", pages 309-314, see pages 310,311, lines 5,6 from the bottom (cited in the application)
Synthesis, no. 5, May 1977, H. Yagi et al.: "Synthesis of 2,6-dimethyl-1,3-trans,7-octatriene (head-to-tail isoprene dimer) by a temperature-controlled two-stage reaction", pages 334-335, see the whole article
Journal of Organometallic Chemistry, vol. 137, no. 3, 20 September 1977, Elsevier Sequoia S.A. Lausanne, R. Klüter et al.: "Die Cooligomerisierung von Butadien mit alpha-Hydroxycarbonsäureestern", pages 309-314, see pages 310,311, lines 5,6 from the bottom (cited in the application)
Synthesis, no. 5, May 1977, H. Yagi et al.: "Synthesis of 2,6-dimethyl-1,3-trans,7-octatriene (head-to-tail isoprene dimer) by a temperature-controlled two-stage reaction", pages 334-335, see the whole article
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