Abstract
ent - Kaurene (1) has been synthesized from a naturally occurring precursor, ent- kaurane - 17,19-diol (3a). Selective deoxygenation at C 19 of the diol was achieved after the C17 hydroxyl was protected as the triphenylmethyl ether. ent- Kaurene was then prepared by way of an elimination sequence at C17.
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.
