Asymmetric trapping of zwitterionic intermediates by sulphur ylides in a palladium-catalysed decarbo...
Asymmetric trapping of zwitterionic intermediates by sulphur ylides in a palladium-catalysed decarboxylation-cycloaddition sequence
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London: Nature Publishing Group UK
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English
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London: Nature Publishing Group UK
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Through nearly 50 years of development, sulphur ylides have been established as versatile and powerful reagents for the construction of carbocycles and heterocycles. Despite advances, two important and yet elusive bottlenecks continue to inhibit the advancement of this chemistry: a limited number of reagents with polar groups to react with sulphur...
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Asymmetric trapping of zwitterionic intermediates by sulphur ylides in a palladium-catalysed decarboxylation-cycloaddition sequence
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TN_cdi_proquest_miscellaneous_1627073308
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1627073308
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2041-1723
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2041-1723
DOI
10.1038/ncomms6500
