The first one-pot oxidative Michael reaction of Baylis-Hillman adducts with indoles promoted by iodoxybenzoic acid

Yadav, J. S. ; Subba Reddy, B. V. ; Pratap Singh, Ashutosh ; Basak, A. K. (2007) The first one-pot oxidative Michael reaction of Baylis-Hillman adducts with indoles promoted by iodoxybenzoic acid Tetrahedron Letters, 48 (24). pp. 4169-4172. ISSN 0040-4039

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2007.04.086

Abstract

Baylis-Hillman adducts undergo smooth, one-pot oxidative conjugate addition with indoles in the presence of 2-iodoxybenzoic acid (IBX) under neutral conditions to afford a new class of substituted indoles in good yields.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Baylis-Hillman Adducts; Hypervalent Iodine; Indoles; Conjugate Addition
ID Code:60390
Deposited On:09 Sep 2011 03:55
Last Modified:09 Sep 2011 03:55

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