| Autor: |
Aadil A. Momin, Tukaram D. Urmode, Shrikar M. Bhosale, Kusurkar, Radhika S. |
| Rok vydání: |
2016 |
| DOI: |
10.6084/m9.figshare.3408013.v1 |
| Popis: |
Three differently substituted naturally occurring, biologically active carbazole derivatives viz. ekeberginine, murrayaquinone A and glycozoline were synthesized in good yield using short and simple routes. Prenyl group was selectively introduced at C4 position using Stille coupling reaction in the synthesis of ekeberginine. Murrayaquinone A was synthesized using Raney nickel mediated desulfurization of dithiane as a key step. Synthesis of glycozoline was achieved in two steps from 3-methyl carbazole via an intermediate 3-bromo-6-methyl carbazole. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
|
