linked to by 1DOI 10.1021/ja910719x PMID 20104842
New reactions of azomethine ylides with nontraditional dipolarophiles are reported. Azomethine ylides, formed in situ via decarboxylative condensations of alpha-amino acids with aldehydes, undergo reactions with naphthols, indoles, alkynes, and nitroalkanes.
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Its been far too long since my last post. Between designing a total synthesis proposal for one of my classes, preparing a manuscript (and supporting information) for a project we are wrapping up, and (in the past week) doing a number of reactions, I’ve...