On the Mechanism of the Nucleophilic Addition to 2,3-Dihydrodipyrrin-1(10H)-ones

DOI: 10.1007/BF00809692

Source and publish data:

Monatshefte fur Chemie p. 793 - 812 (1988)

Update date:2022-08-04

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Authors:

Grubmayr, Karl

Wagner, Ulrike Gabriella

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Article abstract of DOI:10.1007/BF00809692

1H NMR-spectroscopic investigations of the acid catalyzed addition of methanol to dihydrodipyrrinones (Z)-2, (E)-2, and 4 show the C-protonation of their enamide parts to be the first and rate determining step forming the key intermediate, the N-acyl-immo

Full text of DOI:10.1007/BF00809692

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