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Published in 2020 at "ACS Catalysis"
DOI: 10.1021/acscatal.0c02377
Abstract: The tertiary amide is a ubiquitous functional group and plays an irreplaceable role in medicinal chemistry. Its robust nature has meant—in the past—that selective manipulation of this motif remaine...
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Keywords:
using vaska;
reductive functionalization;
amides using;
functionalization tertiary ... See more keywords
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Published in 2017 at "Chemical communications"
DOI: 10.1039/c7cc04170e
Abstract: The development of an efficient protocol for the reductive functionalization of amides into pyrimidinediones and amino-substituted thioacrylamides is presented. Enamines are generated in a highly chemoselective amide hydrosilylation reaction catalyzed by molybdenum hexacarbonyl in combination…
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Keywords:
functionalization amides;
preparation pyrimidinediones;
reductive functionalization;
facile preparation ... See more keywords
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Published in 2021 at "Chemical Science"
DOI: 10.1039/d1sc02819g
Abstract: A mesoionic N-heterocyclic olefin (mNHO) was introduced as a metal-free catalyst for the reductive functionalization of CO2 leading to consecutive double N-methylation of primary amines in the presence of 9-borabicyclo[3.3.1]nonane (9-BBN). A wide range of…
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Keywords:
methylation;
mesoionic heterocyclic;
functionalization co2;
reductive functionalization ... See more keywords