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10.1007/s10593-020-02844-9

http://scihub22266oqcxt.onion/10.1007/s10593-020-02844-9
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33424029!7779642!33424029
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suck abstract from ncbi


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pmid33424029      Chem+Heterocycl+Compd+(N+Y) 2020 ; 56 (12): 1517-1522
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  • Synthetic strategies for pyrrolo 2,1-f 1,2,4 triazine: the parent moiety of antiviral drug remdesivir #MMPMID33424029
  • Rai GS; Maru JJ
  • Chem Heterocycl Compd (N Y) 2020[]; 56 (12): 1517-1522 PMID33424029show ga
  • This review summarizes diverse synthetic protocols for the preparation of pyrrolo[2,1-f][1,2,4]triazine derivatives, covering literature sources from the past two decades. For effective representation, the synthetic methods toward the title compound are classified into six distinct categories: 1) synthesis from pyrrole derivatives, 2) synthesis via bromohydrazone, 3) synthesis via formation of triazinium dicyanomethylide, 4) multistep synthesis, 5) transition metal mediated synthesis, and 6) rearrangement of pyrrolooxadiazines. A brief outline of all optimized schemes is provided with relevant examples.
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