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Synthesis of 1,3,4-oxadiazoles derivatives from -amino acids and acyl hydrazides using microwave irradiation
Synthesis of 1,3,4-oxadiazoles derivatives from -amino acids and acyl hydrazides using microwave irradiation
Martins, Bruna Simões; Heck, Elisiane Frantz; Bender, Caroline Raquel; Filho, Wolmar A. Severo; Braga, Antonio L.; Rodrigues, Oscar E. Dorneles; Dornelles, Luciano
Abstract:
The 1,3,4-oxadiazoles constitute an important family of heterocyclic compounds as they have attracted significant interest in medicinal chemistry, pesticide chemistry and polymer science. These compounds derivatives have been found to exhibit diverse biological activities such as analgesic, antiinflammatory, antimicrobial, anti-HIV and other biological properties. Consequently, the synthesis of compounds containing this heterocycle core has attracted considerable attention and a wide variety of methods have been used for its assembly. By far the most common synthetically protocol involves the dehydrative cyclization of diacylhydrazides, usually with strongly acidic reagents such as SOCl2, P2O5, POCl3 and H2SO4.
The 1,3,4-oxadiazoles constitute an important family of heterocyclic compounds as they have attracted significant interest in medicinal chemistry, pesticide chemistry and polymer science. These compounds derivatives have been found to exhibit diverse biological activities such as analgesic, antiinflammatory, antimicrobial, anti-HIV and other biological properties. Consequently, the synthesis of compounds containing this heterocycle core has attracted considerable attention and a wide variety of methods have been used for its assembly. By far the most common synthetically protocol involves the dehydrative cyclization of diacylhydrazides, usually with strongly acidic reagents such as SOCl2, P2O5, POCl3 and H2SO4.
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DOI: 10.5151/chempro-14bmos-R0364-1
Referências bibliográficas
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Como citar:
Martins, Bruna Simões; Heck, Elisiane Frantz; Bender, Caroline Raquel; Filho, Wolmar A. Severo; Braga, Antonio L.; Rodrigues, Oscar E. Dorneles; Dornelles, Luciano; "Synthesis of 1,3,4-oxadiazoles derivatives from -amino acids and acyl hydrazides using microwave irradiation", p-364-364.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-14bmos-R0364-1
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TY - CONF T1 - Synthesis of 1,3,4-oxadiazoles derivatives from -amino acids and acyl hydrazides using microwave irradiation JO - Blucher Chemistry Proceedings VL - 1 IS - 1 SP - 364 EP - 364 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2011 AU - , , , , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-14bmos-R0364-1 UR - www.proceedings.blucher.com.br/article-details/synthesis-of-134-oxadiazoles-derivatives-from-amino-acids-and-acyl-hydrazides-using-microwave-irradiation-8176 KW - ER -
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@article{Martins20144,
title="Synthesis of 1,3,4-oxadiazoles derivatives from -amino acids and acyl hydrazides using microwave irradiation",
journal="Blucher Chemistry Proceedings",
volume="1",
number="1",
pages="364 - 364",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-14bmos-R0364-1",
url="www.proceedings.blucher.com.br/article-details/synthesis-of-134-oxadiazoles-derivatives-from-amino-acids-and-acyl-hydrazides-using-microwave-irradiation-8176",
author="Bruna Simões Martins", "Elisiane Frantz Heck", "Caroline Raquel Bender", "Wolmar A. Severo Filho", "Antonio L. Braga", "Oscar E. Dorneles Rodrigues", "Luciano Dornelles",
keywords="",
}
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Bruna Simões Martins, Elisiane Frantz Heck, Caroline Raquel Bender, Wolmar A. Severo Filho, Antonio L. Braga, Oscar E. Dorneles Rodrigues, Luciano Dornelles, Synthesis of 1,3,4-oxadiazoles derivatives from -amino acids and acyl hydrazides using microwave irradiation, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 364-364, ISSN 23184043, http://dx.doi.org/10.5151/chempro-14bmos-R0364-1 (www.proceedings.blucher.com.br/article-details/synthesis-of-134-oxadiazoles-derivatives-from-amino-acids-and-acyl-hydrazides-using-microwave-irradiation-8176) Palavras-chave:: ;