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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c03946
Abstract: A novel strategy for the synthesis of (E)-3-((arylsulfonyl)methyl)-4-substituted benzylidenechromene derivatives via a metal-free radical annulation reaction of oxygen-containing 1,7-enynes with thiosulfonates has been developed. The reaction shows broad substrate scope, wide functional group tolerance, and…
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Keywords:
arylsulfonyl methyl;
synthesis arylsulfonyl;
radical annulation;
free radical ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02500
Abstract: A mechanistically distinctive copper-catalyzed radical annulation to valuable 2-(trifluoromethyl)pyrazolo[1,5-a]pyridines and their benzo analogues has been described for the first time. Notably, the newly developed complementary process allows the synthesis of 4- or 6-substituted target molecular…
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Keywords:
pyridines benzo;
catalyzed radical;
radical annulation;
pyrazolo pyridines ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03635
Abstract: A visible-light photocatalytic regioselective [2 + 2 + 1] radical annulation reaction of alkenes, tert-butyl nitrite, and gem-dihalides has been developed. The protocol provides an efficient and practical approach to obtain isoxazolines in good yields…
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Keywords:
gem dihalides;
butyl nitrite;
radical annulation;
photocatalytic regioselective ... See more keywords