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- W1867106068 abstract "Total synthesis of (R)-aporphine has been accomplished by an approach that employs in the key step a sequence of transformations involving a [4+2] cycloaddition reaction followed by a hydrogen migration, leading to aporphine core in good yield, which was subjected to a 1D gradient NOE experiment, conformational analysis, and simple transformations, including a small scale resolution process, to afford enantiomerically enriched aporphine alkaloid." @default.
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- W1867106068 date "2015-12-01" @default.
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- W1867106068 title "A convenient formation of aporphine core via benzyne chemistry: conformational analysis and synthesis of (R)-aporphine" @default.
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- W1867106068 doi "https://doi.org/10.1016/j.tetlet.2015.10.083" @default.
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