Abstract
The extent of intramolecular hydrogen bonding between hydroxyl groups and ring oxygens, as determined by infra-red spectroscopy in the hydroxyl stretching region, in a series of monohydroxy derivatives of tetrahydropyran, tetrahydrofuran and 1:3-dioxan provides direct experimental evidence for the stabilities of different conformations of certain of the alcohols. The synthesis of tetrahydropyran-3-ol is described and the mechanism of the reaction of perbenzoic acid with glycals is discussed.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
