Abstract
A tricyclic intermediate with the potentials to be elaborated to a A-ring aromatic or non-aromatic steroid system, bearing a methyl at C8 carbon, has been synthesized via an oxy-Cope rearrangement from the readily available α-tetralone.
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 19, 1989 - Issue 7-8
![Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days]({"type":"image" , "src" : "/sda/110819/TOC-Subject-Sample-2021-Physical-Sciences.jpg"})
Reprints and Corporate Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Academic Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.
Related Research Data
Pinacol Approach to the Eunicellane Skeleton
Source:
Wiley
Synthesis and biological activity of tetralone abscisic acid analogues
Source:
Royal Society of Chemistry (RSC)
Linking provided by
