STEREOSELECTIVE SYNTHESIS OF (2E,4Z)-DIEN-1-OLS; KEY INTERMEDIATES FOR SYNTHESIS OF SEX PHEROMONES OF SILK WORM AND OF GRAPE VINE MOTH

DOI: 10.1016/S0040-4039(01)80994-1

Source and publish data:

Tetrahedron Letters p. 803 - 804 (1987)

Update date:2022-07-29

Topics:

Authors:

Kuroda, Satoru

Katsuki, Tsutomu

Yamaguchi, Masaru

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Article abstract of DOI:10.1016/S0040-4039(01)80994-1

Two (2E,4Z)-dien-1-ols, synthetic key intermediates for the insect pheromones with a (E,Z)-diene system, were synthesized stereoselectively by using a combination of zirconium-mediated <2,3>Wittig rearrangement reaction and Peterson reaction as key steps.

Full text of DOI:10.1016/S0040-4039(01)80994-1

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Product name:Acetic acid, [[1-cyclohexyl-3-(trimethylsilyl)-2-propenyl]oxy]-, 1-methylethyl ester, (E)-

Cas No:112497-28-6

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