Ушбу иш иқтибос қилган ишлар

35 та иш

Иш: Synthesis of 1,2,3-triazole derivatives based on propargyl ester of a saturated single-basic carbonic acid and para-azidobenzoic acid

1. 1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview

   Khurshed Bozorov, Jiangyu Zhao, Haji Akber Aisa

   Шарҳ мақолаClick Chemistry and ApplicationsBioorganic & Medicinal Chemistry20197 иқтибос

   ABIABI:AkademIndex/openalex/2019.review-article.000001

2. 1,3‐Dipolar Cycloadditions. Past and Future

   Rolf Huisgen

   Мақола19635 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.277011

3. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

   Hartmuth C. Kolb, M. G. Finn, K. Barry Sharpless

   Мақола20014 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.362957

4. Medicinal attributes of 1,2,3-triazoles: Current developments

   Divya Dheer, Virender Singh, Ravi Shankar

   Шарҳ мақола20173 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.003291

5. The importance of triazole scaffold in the development of anticonvulsant agents

   Adileh Ayati, Saeed Emami, Alireza Foroumadi

   Шарҳ мақола20162 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.003287

6. Green synthesis and anticancer potential of chalcone linked-1,2,3-triazoles

   Pinki Yadav, Kashmiri Lal, Ashwani Kumar +3

   Мақола20162 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.193038

7. 1,2,3-Triazoles as Amide Bioisosteres: Discovery of a New Class of Potent HIV-1 Vif Antagonists

   Idrees Mohammed, Indrasena Reddy Kummetha, Gatikrushna Singh +5

   Мақола20162 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.266514

8. Regioselective synthesis and biological evaluation of some novel thiophene-containing heterocyclic scaffolds as potential chemotherapeutic agents

   Hatem M. Gaber, Mark C. Bagley

   Мақола20112 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.535187

9. Peptidotriazoles on Solid Phase:  [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

   Christian W. Tornøe, Caspar Christensen, Morten Meldal

   Мақола20022 иқтибос

   ABIABI:AkademIndex/openalex/2026.other.588082

10. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

    Vsevolod V. Rostovtsev, Luke G. Green, Valery V. Fokin +1

    Мақола20022 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.588085

11. The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview

    Liyuan Liang, Didier Astruc

    Мақола20112 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.594001

12. The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition

    Martin Breugst, Hans‐Ulrich Reißig

    Шарҳ мақола20202 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631567

13. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631544

14. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631545

15. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631546

16. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631547

17. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631548

18. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631549

19. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631550

20. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631551

21. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631552

22. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631553

23. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631554

24. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631555

25. Сарлавҳасиз

    Бошқа1 иқтибос

    ABIABI:AkademIndex/openalex/2026.other.631556