Issue 6, 1970

Stereochemistry and mechanism of base-catalysed rearrangement of hydroxyisopropyldihydrofuranoquinolines. Trapping of an epoxide intermediate

Abstract

The absolute stereochemistry of products from stereospecific base-catalysed rearrangement of (+)-R-balfourodine has been established and a suggested epoxide intermediate has been trapped as its methyl ether.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 337b-338

Stereochemistry and mechanism of base-catalysed rearrangement of hydroxyisopropyldihydrofuranoquinolines. Trapping of an epoxide intermediate

M. F. Grundon and K. J. James, J. Chem. Soc. D, 1970, 337b DOI: 10.1039/C2970000337B

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