#naphthalenes — Public Fediverse posts
Live and recent posts from across the Fediverse tagged #naphthalenes, aggregated by home.social.
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"Here we describe a photoredox-enabled functionalized carbon-atom insertion reaction into #indene. We disclose the utilization of a radical #carbyne precursor that facilitates the insertion of carbon atoms bearing a variety of functional groups, including #trifluoromethyl, #ester, phosphate ester, sulfonate ester, sulfone, nitrile, #amide, aryl ketone and aliphatic #ketone fragments to access a library of 2-substituted #naphthalenes"
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"Here we describe a photoredox-enabled functionalized carbon-atom insertion reaction into #indene. We disclose the utilization of a radical #carbyne precursor that facilitates the insertion of carbon atoms bearing a variety of functional groups, including #trifluoromethyl, #ester, phosphate ester, sulfonate ester, sulfone, nitrile, #amide, aryl ketone and aliphatic #ketone fragments to access a library of 2-substituted #naphthalenes"
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"Here we describe a photoredox-enabled functionalized carbon-atom insertion reaction into #indene. We disclose the utilization of a radical #carbyne precursor that facilitates the insertion of carbon atoms bearing a variety of functional groups, including #trifluoromethyl, #ester, phosphate ester, sulfonate ester, sulfone, nitrile, #amide, aryl ketone and aliphatic #ketone fragments to access a library of 2-substituted #naphthalenes"
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"Here we describe a photoredox-enabled functionalized carbon-atom insertion reaction into #indene. We disclose the utilization of a radical #carbyne precursor that facilitates the insertion of carbon atoms bearing a variety of functional groups, including #trifluoromethyl, #ester, phosphate ester, sulfonate ester, sulfone, nitrile, #amide, aryl ketone and aliphatic #ketone fragments to access a library of 2-substituted #naphthalenes"
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"Here we describe a photoredox-enabled functionalized carbon-atom insertion reaction into #indene. We disclose the utilization of a radical #carbyne precursor that facilitates the insertion of carbon atoms bearing a variety of functional groups, including #trifluoromethyl, #ester, phosphate ester, sulfonate ester, sulfone, nitrile, #amide, aryl ketone and aliphatic #ketone fragments to access a library of 2-substituted #naphthalenes"