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• W3007465111 endingPage "1824" @default.
• W3007465111 startingPage "1818" @default.
• W3007465111 abstract "Sulfonylated N-unsubstituted enamines were synthesized through a chain of chemical and electrochemical transformations via sulfonylation of vinyl azides. The disclosing of the N-unsubstituted enamines synthesis was based on a unique property of the azido group, which is its ability to eliminate the N2 molecule. Furthermore, a formal paradox is observed: a double bond reacts and a double bond is retained. Electrosynthesis proceeded in an undivided cell equipped with a graphite anode and a stainless steel cathode; NH4I was used as a supporting electrolyte." @default.
• W3007465111 created "2020-03-06" @default.
• W3007465111 creator A5034777140 @default.
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• W3007465111 creator A5091732254 @default.
• W3007465111 date "2020-02-20" @default.
• W3007465111 modified "2023-10-02" @default.
• W3007465111 title "Electrochemically Induced Synthesis of Sulfonylated <i>N</i>-Unsubstituted Enamines from Vinyl Azides and Sulfonyl Hydrazides" @default.
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• W3007465111 doi "https://doi.org/10.1021/acs.orglett.0c00139" @default.
• W3007465111 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32077294" @default.
• W3007465111 hasPublicationYear "2020" @default.
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