Synthesis of 2,2'-Biindole: Formal Synthesis of Arcyriaflavin-A and Staurosporinone (K-252c)
Corresponding Author(s) : P.S. Parameswaran
param@nio.org
Asian Journal of Chemistry,
Vol. 24 No. 5 (2012): Vol 24 Issue 5
Abstract
A convenient four-stage synthesis of 2,2'-biindole, the immediate precursor of arcyriaflavin A and staurosporinone via double Wittig-double reductive cyclization reactions is described.
Keywords
Indolocarbazole
Reductive cyclization
2,2'-Biindole
Wittig reaction
Parvatkar, P., Kadam, H., Parameswaran, P., & Tilve, S. (2012). Synthesis of 2,2’-Biindole: Formal Synthesis of Arcyriaflavin-A and Staurosporinone (K-252c). Asian Journal of Chemistry, 24(5), 2213–2215. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/8982
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