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Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles
Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles
Feu, Karla S.; Deobald, Anna M.; Corrêa, Arlene G.; Paixão, Marcio W.
Abstract:
The indole core is featured in a number of natural products as well as medicinally relevant compounds. Recently, the concepts of organocatalytic sequencial reaction has inspired several research groups to design novel stereoselective strategies for assembling target structure and most importantly, reproducing the rich structural diversity found in natural products. Herein, we describe the application of a new class of organocatalysts in the enantioselective synthesis of indole alkaloids under the principles of green chemistry (Figure 1).
The indole core is featured in a number of natural products as well as medicinally relevant compounds. Recently, the concepts of organocatalytic sequencial reaction has inspired several research groups to design novel stereoselective strategies for assembling target structure and most importantly, reproducing the rich structural diversity found in natural products. Herein, we describe the application of a new class of organocatalysts in the enantioselective synthesis of indole alkaloids under the principles of green chemistry (Figure 1).
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DOI: 10.5151/chempro-14bmos-R0342-1
Referências bibliográficas
- [1] 1 Bandini,M.; Eichholzer, A. Angew. Chem. Int. Ed. 2009, 48, 9608.
- [2] 2 Brandau,S.; Landa,A.; Franzén, J.;Marigo, M.; Jørgensen, K. A. Angew. Chem. Int. Ed. 2006, 45, 4305.
Como citar:
Feu, Karla S.; Deobald, Anna M.; Corrêa, Arlene G.; Paixão, Marcio W.; "Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles", p-342-342.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-14bmos-R0342-1
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TY - CONF T1 - Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles JO - Blucher Chemistry Proceedings VL - 1 IS - 1 SP - 342 EP - 342 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2011 AU - , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-14bmos-R0342-1 UR - www.proceedings.blucher.com.br/article-details/tandem-organocatalytic-functionalization-and-fisher-indole-synthesis-a-greener-approach-for-the-synthesis-of-indoles-8161 KW - ER -
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@article{Feu20144,
title="Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles",
journal="Blucher Chemistry Proceedings",
volume="1",
number="1",
pages="342 - 342",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-14bmos-R0342-1",
url="www.proceedings.blucher.com.br/article-details/tandem-organocatalytic-functionalization-and-fisher-indole-synthesis-a-greener-approach-for-the-synthesis-of-indoles-8161",
author="Karla S. Feu", "Anna M. Deobald", "Arlene G. Corrêa", "Marcio W. Paixão",
keywords="",
}
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Karla S. Feu, Anna M. Deobald, Arlene G. Corrêa, Marcio W. Paixão, Tandem Organocatalytic Functionalization and Fisher Indole Synthesis: A Greener Approach for the Synthesis of Indoles, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 342-342, ISSN 23184043, http://dx.doi.org/10.5151/chempro-14bmos-R0342-1 (www.proceedings.blucher.com.br/article-details/tandem-organocatalytic-functionalization-and-fisher-indole-synthesis-a-greener-approach-for-the-synthesis-of-indoles-8161) Palavras-chave:: ;