Issue 0, 1974

Some attempts to use the modified acyloin reaction of Schräpler and Rühlmann for the synthesis of strained carbocylic systems

Abstract

Dimethyl trans-cyclopropane-1,2-diacetate (I) and dimethyl trans-oct-4-ene-1,8-dioate (II) failed to undergo cyclisation under the conditions of the modified acyloin reaction. Dimethyl cis- and trans-cyclopropane-1,2-dicarboxylate underwent reductive cleavage with formation of 1,5-dimethoxy-1,5-bis(trimethylsilyloxy)penta-1,4-diene (IV).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 879-881

Some attempts to use the modified acyloin reaction of Schräpler and Rühlmann for the synthesis of strained carbocylic systems

C. U. L. Delbaere and G. H. Whitham, J. Chem. Soc., Perkin Trans. 1, 1974, 879 DOI: 10.1039/P19740000879

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