Issue 0, 1982

Keten silyl acetal chemistry; simple synthesis of methyl jasmonate and related compounds by utilising keten methyl dimethyl-t-butylsilyl acetal

Abstract

Conjugate addition of keten silyl acetals to α,β-unsaturated carbonyl compounds in acetonitrile gave a quantitative yield of the corresponding methyl (3-trialkylsiloxyalk-2-enyl)acetates; subsequent site-specific electrophilic substitution yielded the corresponding 2-substituted 3-(alkoxycarbonylmethyl)alkanones. These novel addition and sequential alkylation reactions could be applied to a simple synthesis of methyl jasmonate, methyl didehydrojasmonate, and methyl dihydrojasmonate.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 1099-1104

Keten silyl acetal chemistry; simple synthesis of methyl jasmonate and related compounds by utilising keten methyl dimethyl-t-butylsilyl acetal

Y. Kita, J. Segawa, J. Haruta, H. Yasuda and Y. Tamura, J. Chem. Soc., Perkin Trans. 1, 1982, 1099 DOI: 10.1039/P19820001099

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements