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Microwaves promoted an efficient synthesis of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydropyrazoles
Microwaves promoted an efficient synthesis of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydropyrazoles
Ritter, Marina; Rosa, Silvana Alves; Silva, Caroline Carapina da; Flores, Alex C. F.; Pizzuti, Lucas; Pereira, Claudio Martin Pereira de
Abstract:
Pyrazoles are a class of heterocycles with five members, containing two atoms of nitrogen in adjacent positions. Diverse ranges of biological properties are associated with these molecules, including antimicrobial, antitumor, anti-inflammatory, antiviral, anticonvulsant and antidepressant activities. The current situation of environmental degradation demands from the chemical community the development of more efficient and cleaner methodologies in regard to energy consumption and reduction of waste. In agreement with this demand, we prepared several classes of heterocyclic compounds by non-conventional methods such as microwaves and sonochemistry. The success of microwave technology is based on the dipole rotation, which is responsible for heating the substances efficiently, occurring directly in the molecules. In this work, we report the synthesis of pyrazoles derivated from chalcones under microwave irradiation
Pyrazoles are a class of heterocycles with five members, containing two atoms of nitrogen in adjacent positions. Diverse ranges of biological properties are associated with these molecules, including antimicrobial, antitumor, anti-inflammatory, antiviral, anticonvulsant and antidepressant activities. The current situation of environmental degradation demands from the chemical community the development of more efficient and cleaner methodologies in regard to energy consumption and reduction of waste. In agreement with this demand, we prepared several classes of heterocyclic compounds by non-conventional methods such as microwaves and sonochemistry. The success of microwave technology is based on the dipole rotation, which is responsible for heating the substances efficiently, occurring directly in the molecules. In this work, we report the synthesis of pyrazoles derivated from chalcones under microwave irradiation
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DOI: 10.5151/chempro-15bmos-BMOS2013_2013929214759
Referências bibliográficas
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Como citar:
Ritter, Marina; Rosa, Silvana Alves; Silva, Caroline Carapina da; Flores, Alex C. F.; Pizzuti, Lucas; Pereira, Claudio Martin Pereira de; "Microwaves promoted an efficient synthesis of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydropyrazoles", p-294-294.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 2, Dezembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-15bmos-BMOS2013_2013929214759
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TY - CONF T1 - Microwaves promoted an efficient synthesis of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydropyrazoles JO - Blucher Chemistry Proceedings VL - 1 IS - 2 SP - 294 EP - 294 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2013 AU - , , , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013929214759 UR - www.proceedings.blucher.com.br/article-details/microwaves-promoted-an-efficient-synthesis-of-1-thiocarbamoyl-35-diaryl-45-dihydropyrazoles-8514 KW - ER -
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@article{Ritter20144,
title="Microwaves promoted an efficient synthesis of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydropyrazoles",
journal="Blucher Chemistry Proceedings",
volume="1",
number="2",
pages="294 - 294",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013929214759",
url="www.proceedings.blucher.com.br/article-details/microwaves-promoted-an-efficient-synthesis-of-1-thiocarbamoyl-35-diaryl-45-dihydropyrazoles-8514",
author="Marina Ritter", "Silvana Alves Rosa", "Caroline Carapina da Silva", "Alex C. F. Flores", "Lucas Pizzuti", "Claudio Martin Pereira de Pereira",
keywords="",
}
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Marina Ritter, Silvana Alves Rosa, Caroline Carapina da Silva, Alex C. F. Flores, Lucas Pizzuti, Claudio Martin Pereira de Pereira, Microwaves promoted an efficient synthesis of 1-thiocarbamoyl-3,5-diaryl-4,5-dihydropyrazoles, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 294-294, ISSN 23184043, http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_2013929214759 (www.proceedings.blucher.com.br/article-details/microwaves-promoted-an-efficient-synthesis-of-1-thiocarbamoyl-35-diaryl-45-dihydropyrazoles-8514) Palavras-chave:: ;