Dergiler / Turkish Journal of Chemistry / 2018 / Cilt: 42 - Sayı: 6

Recent synthetic methodologies for pyrimidine and its derivatives

Sayfa
1421–1458
Yayın Tarihi
2022-11-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

In this context, the present reviewillustrates a variety of novel and efficient synthetic approaches towards the synthesis of pyrimidine and its derivativesthat were reported recently.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Pyrimidine derivatives are well known due to their remarkable pharmacological potential in various fields ofscience, and they are also present in some natural substances like DNA and RNA.
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Temel Bulgular & Veri:These scaffolds manifest diversifiedbiological activities such as antimicrobial, antiinflammatory, anti-HIV, antitubercular, antitumor, antineoplastic, andantimalarial.
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Sonuç & Katkı:In this context, the present reviewillustrates a variety of novel and efficient synthetic approaches towards the synthesis of pyrimidine and its derivativesthat were reported recently.
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Pyrimidine derivatives are well known due to their remarkable pharmacological potential in various fields ofscience, and they are also present in some natural substances like DNA and RNA. These scaffolds manifest diversifiedbiological activities such as antimicrobial, antiinflammatory, anti-HIV, antitubercular, antitumor, antineoplastic, andantimalarial. A pyrimidine ring is constructed when chalcones, amidines, guanidine, nitriles, isocyanates, urea, thiourea,and aminopyrazoles undergo condensation, coupling, or cyclization reactions. In this context, the present reviewillustrates a variety of novel and efficient synthetic approaches towards the synthesis of pyrimidine and its derivativesthat were reported recently.

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Bu Makaleye Atıf Yap

AHMAD, M., IBRAHEEM, F., SADDIQUE, F. A., MANSHA, A., ASLAM, S., FAROOQ, T. (2022). Recent synthetic methodologies for pyrimidine and its derivatives. Turkish Journal of Chemistry, Cilt: 42 - Sayı: 6, 1421–1458. https://ajindex.com/articles/601821

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Kaynakça (26)

  1. Sasada, T.; Kobayashi, F.; Sakai, N.; Konakahara, T. Org. Lett. 2009, 11, 2161-2164
  2. Dinakaran, V. S.; Bomma, B.; Srinivasan. K. K. Der Pharma Chem. 2012, 4, 255-265
  3. Pratyusha, C.; Poornima, G.; Rani, K. S.; Krishnaveni, A.; Brahmaiah, B.; Nama, S. Int. J. Pharm. Sci. Rev. Res. 2013, 3, 86-90
  4. Jain, K. S.; Chitre, T. S.; Miniyar, P. B.; Kathiravan, M. K.; Bendre, V. S.; Veer, V. S.; Shahane, S. R.; Shishoo, C. J. Curr. Sci. 2006, 90, 793-803
  5. Sathisha, K. R.; Gopal, S.; Rangapp, K. S. World J. Pharm. Res. 2015, 5, 1467-1491
  6. Desai, N. C.; Kotadiya, G. M.; Trivedi, A. R. Bioorg. Med. Chem. Lett. 2014, 24, 3126-3130
  7. Said, S. A.; Abdulla, M. M. World Appl. Sci. J. 2010, 9, 589-599
  8. Kashyap, S. J.; Sharma, P. K.; Garg, V. K.; Dudhe, R.; Kumar, N. J. Adv. Sci. Res. 2011, 2, 18-24
  9. Azas, N.; Rathelot, P.; Djekou, S.; Delmas, F.; Gellis, A.; Giorgio, C. D.; Vanelle, P.; Timon-David, P. Farmaco 2003, 58, 1263-1270
  10. Arulkumaran, R.; Sundararajan, R.; Manikandan, V.; Sathiyendiran, V.; Pazhamalai, S.; Thirunarayanan, G. Int. Lett. Chem. Phys. Astron. 2014, 19, 15-25
  11. Asiri, A. M.; Khan, S. A. Molecules 2011, 16, 523-531
  12. Gupta, R. Int. J. Comput. Appl. 2015, 2015, 0975-8887
  13. Alodeani, E. A.; Izhari, M. A.; Arshad, M. European Journal of Biomedical and Pharmaceutical Sciences 2014, 1, 504-527
  14. Falsone, F. S.; Kappe, C. O. Arkivoc 2001, 122-134
  15. Adib, M.; Yavari, H.; Mollahosseini, M. Tetrahedron Lett. 2004, 45, 1803-1805
  16. Adib, M.; Sayahi, M. H; Ziyadi, H.; Bijanzadeh, H. R.; Zhu, L. Tetrahedron 2007, 63, 11135-11140
  17. Dandia, A.; Sarawgi, P.; Arya, K.; Khaturia, S. Arkivoc 2006, 83-95
  18. Sheibani, H.; Saljoogi, A. S.; Bazgir, A. Arkivoc 2008, 115-123
  19. Sasada, T.; Kobayashi, F.; Sakai, N.; Konakahara, T. Org. Lett. 2009, 11, 2161-2164
  20. Pansuriya, A. M.; Savant, M. M.; Bhuva, C. V.; Singh, J.; Naliapara, Y. T. Arkivoc 2009, 79-85
  21. Majumder, S.; Odom, A. L. Tetrahedron 2010, 66, 3152-3158
  22. Heravi, M. M.; Sadjadi, S.; Oskooie, H. A.; Shoar, R. H.; Bamoharram, F. F. Tetrahedron Lett. 2009, 50, 662-666
  23. Chowrasia, R.; Katla, R.; Darbem, M. P.; Branquinho, T. A.; Oliveira, A. R. D. O.; Manjari, P. S.; Domingues, N. L. C. Tetrahedron Lett. 2016, 57, 1656-1660
  24. Saikia, P.; Gogoi, S.; Gogoi, S. C. Steroids 2014, 88, 1-6
  25. Rao, G. B. D.; Acharya, B. N.; Verma, S. K.; Kaushik, M. P. Tetrahedron Lett. 2011, 52, 809-812
  26. Nagarapu, L.; Vanaparthi, S.; Bantu, R.; Kumar, C. G. Eur. J. Med. C