Abstract
A route to the functionalised cyclopentenone derivative, (2 S)-( 2 3 )-dibenzyloxy-5-(hydroxymethyl)cyclopentene-4-enone ethylene acetal, has been developed from a deoxyinosose that is readily accessible. The carbocyclisation procedure was less efficient in affording (2 S)-(2, 3 4 ,5)-2,3,4,5-tetrahydroxy-2,3- O-isopropylidenecyclohexanone from 6-deoxy-1,2:3,4-di- O-isopropylidene-β- l- arabino-hex-5-enopyranose. Various reactions were carried out on (2 S)-(2,4, 5 3 )-2,3-di-benzoyloxy-5-hydroxy-4-toluene- p-sulphonyloxycyclohexanone ethylene dithioacetal.
Sign-in/Register to access full text options 
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 callSimilar Papers
Disclaimer: 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.
