The Friedel-Crafts Arylation of α-Substituted Chalcones Revisited: Highly Stereospecific Synthesis of TRANS-2,3-Diphenyl-Indan-1-One Derivatives # : Synthetic Communications: Vol 26, No 22

Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 26, 1996 - Issue 22

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Abstract

The Lewis or protic acid promoted cycloisomerization of 1,2,3-triphenylpropenone in nitroethane as solvent has given trans-2,3-diphenyl-indan-1-one with complete diastereoselection in good to excellent chemical yield.

This paper is dedicated with respect to Professor Manuel Bernabé Pajares on occasion of his 60th birthday

Notes

This paper is dedicated with respect to Professor Manuel Bernabé Pajares on occasion of his 60th birthday

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The Friedel-Crafts Arylation of α-Substituted Chalcones Revisited: Highly Stereospecific Synthesis of TRANS-2,3-Diphenyl-Indan-1-One DerivativesFootnote^#
This paper is dedicated with respect to Professor Manuel Bernabé Pajares on occasion of his 60th birthday

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The Friedel-Crafts Arylation of α-Substituted Chalcones Revisited: Highly Stereospecific Synthesis of TRANS-2,3-Diphenyl-Indan-1-One DerivativesFootnote#This paper is dedicated with respect to Professor Manuel Bernabé Pajares on occasion of his 60th birthday

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The Friedel-Crafts Arylation of α-Substituted Chalcones Revisited: Highly Stereospecific Synthesis of TRANS-2,3-Diphenyl-Indan-1-One DerivativesFootnote^#
This paper is dedicated with respect to Professor Manuel Bernabé Pajares on occasion of his 60th birthday