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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b02218
Abstract: A novel method for the regioselective synthesis of 4-arylpyrimido[1,2-b]indazoles has been developed via the dual C(sp3)-H bond functionalization and C-N bond cleavage of triethylamine. The elusive acyclic enamine intermediates are effectively in situ generated and…
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Keywords:
arylpyrimido indazoles;
synthesis arylpyrimido;
bond;
bond cleavage ... See more keywords