Synthesis of tryptanthrin and deoxyvasicinone by a regioselective lithiation-intramolecular electrophilic reaction approach

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Abstract

An efficient synthesis of the 4(3H)-quinazolinone-based alkaloids, tryptanthrin and deoxyvasicinone has been achieved in good overall yields by using the strategy of regioselective lithiation-intramolecular electrophilic reaction as a key-step. Both the molecules have been synthesized in just two-steps from readily available starting materials. ©ARKAT USA, Inc.

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CITATION STYLE

APA

Potewar, T. M., Ingale, S. A., & Srinivasan, K. V. (2008). Synthesis of tryptanthrin and deoxyvasicinone by a regioselective lithiation-intramolecular electrophilic reaction approach. Arkivoc, 2008(14), 100–108. https://doi.org/10.3998/ark.5550190.0009.e11

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