Synthesis

A new synthesis of ω-hydroxyalkanoic acids via copper catalysis

D Villemin, P Cadiot, M Kuétegan

Index: Villemin, Didier; Cadiot, Paul; Kuetegan, Mikem Synthesis, 1984 , # 3 p. 230 - 231

Full Text: HTML

Citation Number: 19

Abstract

© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular ...

Related Articles:

Macrocyclic musk compounds—IV: New syntheses of α, ω-dicarboxylic and ω-hydroxy acids from undec-10-enoic acid

[Nair,M.S.R. et al. Tetrahedron, 1963 , vol. 19, p. 905 - 909]

452. Macrocyclic musk compounds. Part I. New syntheses of exaltolide, exaltone, and dihydrocivetone

[Dhekne,V.V. et al. Journal of the Chemical Society, 1962 , p. 2348 - 2352]

A macrolactonization approach to the total synthesis of the antimicrobial cyclic depsipeptide LI-F04a and diastereoisomeric analogues

[Cochrane, James R.; Yoon, Dong Hee; McErlean, Christopher S.P.; Jolliffe, Katrina A. Beilstein Journal of Organic Chemistry, 2012 , vol. 8, p. 1344 - 1351]

1121. Syntheses of long-chain acids. Part V. Synthesis of some ω-hydroxy-acetylenic acids

[Ames,D.E. et al. Journal of the Chemical Society, 1963 , p. 5889 - 5893]

452. Macrocyclic musk compounds. Part I. New syntheses of exaltolide, exaltone, and dihydrocivetone

[Dhekne,V.V. et al. Journal of the Chemical Society, 1962 , p. 2348 - 2352]

More Articles...