Zinc-mediated acylation and sulfonation of pyrrole and its derivatives
JS Yadav, BVS Reddy, G Kondaji, RS Rao, SP Kumar
Index: Yadav; Reddy; Kondaji; Srinivasa Rao; Praveen Kumar Tetrahedron Letters, 2002 , vol. 43, # 45 p. 8133 - 8135
Full Text: HTML
Citation Number: 32
Abstract
The 2-ketopyrrole moiety, although rarely reported, is apparently biologically important as evidenced by its presence in naturally occurring molecules such as X-14547A, 1., and and A-23187 (calcimycin). 2 Generally, 2-acetyl pyrroles are prepared by the Vilsmeier–Haack method using POCl 3 and N,N-dimethylacetamide. 3., , , and Other methods for the acylation of pyrroles involve the isomerization of N-acetyl pyrroles by thermal rearrangement at high temperature, ...
Related Articles:
Synthesis and rearrangement of pyrrolyl sulfides and sulfones
[DeSales, Javier; Greenhouse, Robert; Muchowski, Joseph M. Journal of Organic Chemistry, 1982 , vol. 47, p. 3668 - 3672]
Ortho-metallation reactions of various N-substituted pyrroles
[Cartoon, M. E. K.; Cheeseman, G. W. H. Journal of Organometallic Chemistry, 1982 , vol. 234, # 2 p. 123 - 136]
Synthesis and rearrangement of pyrrolyl sulfides and sulfones
[DeSales, Javier; Greenhouse, Robert; Muchowski, Joseph M. Journal of Organic Chemistry, 1982 , vol. 47, p. 3668 - 3672]