Type of Material: | Thesis |
Title: | Applications of Ugi Sonogashira and Barbier reactions Metal electrophile catalyzed synthesis of pyridine pyrrole pyran and thiopyran fused quinoline heterocycles |
Researcher: | Asthana, Mrityunjaya |
Guide: | Singh, R.M. |
Department: | Department of Chemistry |
Publisher: | Banaras Hindu University,Varanasi |
Place: | Varanasi |
Year: | 2015 |
Language: | English |
Subject: | Copper-catalyzed | One-pot | Ugi reaction | Life Science |
Dissertation/Thesis Note: | PhD; Department of Chemistry, Banaras Hindu University,Varanasi, Varanasi; 2015 |
Fulltext: | Shodhganga |
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035 | __ | |a(IN-AhILN)th_452210 |
040 | __ | |aBHUL_221005|dIN-AhILN |
041 | __ | |aeng |
100 | __ | |aAsthana, Mrityunjaya|eResearcher |
110 | __ | |aDepartment of Chemistry|bBanaras Hindu University,Varanasi|dVaranasi|ein |
245 | __ | |aApplications of Ugi Sonogashira and Barbier reactions Metal electrophile catalyzed synthesis of pyridine pyrrole pyran and thiopyran fused quinoline heterocycles |
260 | __ | |aVaranasi|bBanaras Hindu University,Varanasi|c2015 |
300 | __ | |dDVD |
502 | __ | |bPhD|cDepartment of Chemistry, Banaras Hindu University,Varanasi, Varanasi|d2015 |
518 | __ | |oDate of Registration|d2009-09-01 |
520 | __ | |aQuinoline is a heterocyclic scaffold of paramount importance to human race. Severalnewlineannulated quinoline derivatives possess variety of biological activities such as antimalarial,newlineantibacterial, antifungal, and anticancer agents. Similarly, hetero-annulated quinolines inhibitnewlineDNA topoisomerase I, and display cytotoxic and antitumor activities. Owing to their broadnewlinebiological applications, the synthesis of hetero-annulated quinolines has become a subject ofnewlinegreat importance to organic and medicinal chemists.newlineAccordingly, the research work embodied in the dissertation entitled Applications ofnewlineUgi, Sonogashira and Barbier reactions: Metal/electrophile-catalyzed synthesis ofnewlinepyridine, pyrrole, pyran and thiopyran-fused quinoline heterocycles deals withnewlineapplications of Ugi, Sonogashira and Barbier reactions to the synthesis of pyridine-, pyrrole-,newlinepyran- and thiopyrans-annulated quinolines, which are divided in two parts. Part I containsnewlinethe impo |
650 | __ | |aLife Science|2AIU |
653 | __ | |aCopper-catalyzed |
653 | __ | |aOne-pot |
653 | __ | |aUgi reaction |
700 | __ | |aSingh, R.M.|eGuide |
856 | __ | |uhttp://shodhganga.inflibnet.ac.in/handle/10603/218636|yShodhganga |
905 | __ | |afromsg |
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