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Bradley, L.M., Collins, C.G., Tabakin, E.R. and Hunt, D.A. (2010) Expedient Preparation of 4,6-Dihalo-3-Aryliso- benzofuran-1(3H)-Ones from 3,5-Dihalo-N-Ethylbenzamides. Organic Preparations and Procedures International, 42, 187-190.
http://dx.doi.org/10.1080/00304941003727045

has been cited by the following article:

• TITLE: Regioselectivity Differentiation in Metalations of 3,5-Dichloro-Tertiary versus Secondary Benzamides

  AUTHORS: Francesca Khani, Tina Fleming, Carleton Collins, Erica Tabakin, Lynn M. Bradley, David A. Hunt

  KEYWORDS: Directed Ortho-Metalation, Complex-Induced Proximity Effects (CIPE), 3, 5-Dichlorobenzamides

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.2, June 3, 2016

  ABSTRACT: Metalation regioslectivity of 3,5-dichlorobenzamides is a function of the type of amide (secondary versus tertiary) used in the sequence. Metalation at the 2-position (adjacent to the carboxamide functional group) occurs when the secondary benzamide is metalated with sec-butyllithium/ TMEDA mediated through complex-induced proximity effects (CIPE) process, whereas metalation with sec-butyllithium/TMEDA occurs exclusively at the 4-position when the tertiary benzamide is used under identical reaction conditions.