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Published in 2020 at "Organic chemistry frontiers"
DOI: 10.1039/d0qo00024h
Abstract: A cyanomethylation of α,β-unsaturated aldehydes with acetonitrile as a nucleophile is disclosed. The reaction is promoted with Cu2O as an inexpensive catalyst. Mild conditions are used, and the reaction completes within a few minutes. Through…
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Keywords:
unsaturated aldehydes;
acetonitrile unsaturated;
catalyzed selective;
addition acetonitrile ... See more keywords
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1
Published in 2022 at "Chemical Science"
DOI: 10.1039/d2sc01690g
Abstract: Main group organometallic compounds can exhibit unusual optical properties arising from hybrid σ,π-conjugation. While linear silanes are extensively studied, the shortage of methods for the controlled synthesis of well-defined cyclic materials has precluded the study…
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Keywords:
addition;
alkynes enabling;
cyclosilanes alkynes;
selective addition ... See more keywords
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2
Published in 2023 at "Chemical Science"
DOI: 10.1039/d2sc05674g
Abstract: Transition-metal catalyzed functionalization of ACPs has been widely investigated in cycloaddition and 1,3-difunctionalization reactions. However, the transition metal catalyzed nucleophilic reactions of ACPs have rarely been reported. In this article, an enantio-, site- and E/Z-selective…
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Keywords:
site selective;
palladium nsted;
nsted acid;
selective addition ... See more keywords