Srinivasa Rao, Ch. ; Balu, Maliakel P. ; Ila, Hiriyakkanavar ; Junjappa, Hiriyakkanavar (1991) Cycloaromatization of α-oxoketene dithioacetals and β-oxodithioacetals with benzyl-,1-(naphthylmethyl) and 2-(naphthylmethyl)magnesium halides: synthesis of condensed polynuclear aromatic hydrocarbons Tetrahedron, 47 (20-21). pp. 3499-3510. ISSN 0040-4020
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/S0040-4020(01)86411-5
Abstract
An efficient route for the synthesis of substituted naphthalenes, phenanthrenes and other polynuclear aromatic hydrocarbons has been developed. The methodology involves 1,2- (or sequential 1,4- and 1,2-) addition of either benzyl, 1-(naphthylmethyl) or 2-(naphthylmethyl) magnesium halides to α-oxoketene dithioacetals or β-oxodithioacetals followed by borontrifluoride etherate catalyzed cycloaromatization of the resulting carbinols.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
ID Code: | 24078 |
Deposited On: | 29 Nov 2010 10:29 |
Last Modified: | 22 Feb 2011 05:04 |
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