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Synthesis of meso-tetra-(5-iodo-thien-2-yl)-porphyrin; an intermediate for cross-coupling reactions
Synthesis of meso-tetra-(5-iodo-thien-2-yl)-porphyrin; an intermediate for cross-coupling reactions
Donatoni, Maria C.; Vieira, Ygor W.; Brocksom, Timothy J.; Oliveira, Kleber T. de
Abstract:
The synthesis of new porphyrins has become a major challenge, mainly due to their wide range of applications, including photochemical cells and photodynamic therapy (PDT). With the advent of one-pot processes for the synthesis of meso substituted porphyrins, the number of these compounds has increased considerably. Porphyrins with meso-thienyl groups can also be used as building blocks for new porphyrins. One way to functionalize these compounds is the Heck-Mizoroki and Sonogashira cross coupling reactions. We now propose the synthesis of meso-thien-2-yl-porphyrins functionalized with iodine, ready for cross-coupling reactions.
The synthesis of new porphyrins has become a major challenge, mainly due to their wide range of applications, including photochemical cells and photodynamic therapy (PDT). With the advent of one-pot processes for the synthesis of meso substituted porphyrins, the number of these compounds has increased considerably. Porphyrins with meso-thienyl groups can also be used as building blocks for new porphyrins. One way to functionalize these compounds is the Heck-Mizoroki and Sonogashira cross coupling reactions. We now propose the synthesis of meso-thien-2-yl-porphyrins functionalized with iodine, ready for cross-coupling reactions.
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DOI: 10.5151/chempro-15bmos-BMOS2013_201391315336
Referências bibliográficas
- [1] 1. Horn, S.; Dahms, K.; Senge, M. O.; J. Porphyrins Phthalocyanines 2008, 12, 1053.
- [2] 2. Lindsey, J. S.; Kadish, K. M.; Smith, K. M.; Guilard, R. In The Porphyrin Handbook, Vol. 1; Eds. Academic Press: San Diego, 2000, 45.
- [3] 3. Prasath, R., Bhavana, P. J. Het. Chem. 2012, 49, 1044.
- [4] 4. Murray, P. M.; Bower, J. F.; Cox, D. K.; Galbraith, E. K.; Parker, J. S.; Sweeney, J. B. Org. Process Res. Dev. 2013, 17, 397.
- [5] 5. Davis, M. C.; Baldwin, L.C.; Groshens, T. J. Tetrahedron Lett. 2012, 53, 1564.
Como citar:
Donatoni, Maria C.; Vieira, Ygor W.; Brocksom, Timothy J.; Oliveira, Kleber T. de; "Synthesis of meso-tetra-(5-iodo-thien-2-yl)-porphyrin; an intermediate for cross-coupling reactions", p-73-73.
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_201391315336
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TY - CONF T1 - Synthesis of meso-tetra-(5-iodo-thien-2-yl)-porphyrin; an intermediate for cross-coupling reactions JO - Blucher Chemistry Proceedings VL - 1 IS - 2 SP - 73 EP - 73 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2013 AU - , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_201391315336 UR - www.proceedings.blucher.com.br/article-details/synthesis-of-meso-tetra-5-iodo-thien-2-yl-porphyrin-an-intermediate-for-cross-coupling-reactions-8293 KW - ER -
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@article{Donatoni20144,
title="Synthesis of meso-tetra-(5-iodo-thien-2-yl)-porphyrin; an intermediate for cross-coupling reactions",
journal="Blucher Chemistry Proceedings",
volume="1",
number="2",
pages="73 - 73",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_201391315336",
url="www.proceedings.blucher.com.br/article-details/synthesis-of-meso-tetra-5-iodo-thien-2-yl-porphyrin-an-intermediate-for-cross-coupling-reactions-8293",
author="Maria C. Donatoni", "Ygor W. Vieira", "Timothy J. Brocksom", "Kleber T. de Oliveira",
keywords="",
}
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Maria C. Donatoni, Ygor W. Vieira, Timothy J. Brocksom, Kleber T. de Oliveira, Synthesis of meso-tetra-(5-iodo-thien-2-yl)-porphyrin; an intermediate for cross-coupling reactions, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 73-73, ISSN 23184043, http://dx.doi.org/10.5151/chempro-15bmos-BMOS2013_201391315336 (www.proceedings.blucher.com.br/article-details/synthesis-of-meso-tetra-5-iodo-thien-2-yl-porphyrin-an-intermediate-for-cross-coupling-reactions-8293) Palavras-chave:: ;