347. Stereochemical studies of olefinic compounds. Part III. Ring scission of 3-halogeno-2-alkyltetrahydrofurans as a route to alk-3-en-1-ols of known configuration and as a method of chain extension by four methylene groups
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1950/JR/JR9500001714
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1. Analysis of secretions from scent-producing glands of brushtail possum (Trichosorus vulpecula Kerr);Journal of Chemical Ecology;1994-02
2. Stereoselective synthesis of alcohols containing (Z)- and (E)-olefins, dienes, enynes and styrenes: cyclic β-halogeno ether scissions using samarium diiodide as the electron-transfer agent;J. Chem. Soc., Perkin Trans. 1;1994
3. Urea as the most reactive and versatile nitrogen nucleophile for the palladium(2+)-catalyzed cyclization of unsaturated amines;Journal of the American Chemical Society;1988-06
4. Magnesium ring scission reaction of 2-alkyl-3-chlorotetrahydropyrans;Acta Chimica Sinica;1988-05
5. Total synthesis of (±)-β-bulnesene via intramolecular cycloaddition of a 2-substituted 3-oxidopyrylium;J. Chem. Soc., Perkin Trans. 1;1985
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