Issue 1, 1972

Acid versus base hydrolysis of a disulphonylated hexitol. 1,4,3,6-Dianhydro-D-iditol (D-isoidide)versus 2,3:4,5-dianhydro-D-iditol

Abstract

Whereas acid hydrolysis of 3,4-di-O-methylsulphonyl-D-mannitol (2) produces 1,4-anhydro-3-O-methylsulphonyl-D-talitol (4) and thereafter 1,4:3,6-dianhydro-D-iditol (3), base hydrolysis of the ester (2) gives isomeric 2,3:4,5-dianhydro-D-iditol (8) exclusively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 19-20

Acid versus base hydrolysis of a disulphonylated hexitol. 1,4,3,6-Dianhydro-D-iditol (D-isoidide)versus 2,3:4,5-dianhydro-D-iditol

B. Fraser-Reid and D. R. Hicks, J. Chem. Soc., Chem. Commun., 1972, 19 DOI: 10.1039/C39720000019

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