Abstract
The half esters, resulting from the Stobbe condensation of α-tetralone with succinic esters, on cyclization give the keto-ester “ethyl 3-ketoΔ 8-6,7-benzhydrindan-1-carboxylate”. This on Clemmensen reduction yields the corresponding αβ-unsaturated ester, from which 6,7-benzhydrindan-1-carboxylic acid was prepared by catalytic reduction and hydrolysis and this acid 6,7-benzhydrindan-1-hydroxymethyl ketone and its acetate were prepared.
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 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.
