Tetrahedron Letters

The rate retarding effect of alkyl groups on arene metalation quantified

E Baston, Q Wang, M Schlosser

Index: Baston, Eckhard; Wang, Qian; Schlosser, Manfred Tetrahedron Letters, 2000 , vol. 41, # 5 p. 667 - 670

Full Text: HTML

Citation Number: 12

Abstract

Metalation/trapping sequences applied to relatively inert, tert-alkyl substituted arenes tend to give poor yields unless the reagent is used in high concentrations. Under optimized conditions, even 1, 4-bis (tert-butyl) benzene, 1, 1, 3, 3-tetramethylindane and 1, 1, 2, 2, 3, 3- hexamethylindane can be smoothly converted into derivatives. Competition experiments enable the quantitative assessment of tert-alkyl substituent effects on the metalation rates ...

Related Articles:

Dimetalation: the acidity of monometalated arenes towards superbasic reagents

[Baston, Eckhard; Maggi, Raimondo; Friedrich, Kirstin; Schlosser, Manfred European Journal of Organic Chemistry, 2001 , # 21 p. 3985 - 3989]

Preparation of some 4??or 5??substituted 2??tert. butylbenzoic acids

[Baas,J.M.A.; Wepster,B.M. Recueil des Travaux Chimiques des Pays-Bas, 1967 , vol. 86, p. 69 - 79]

More Articles...