Nucleophilic Aromatic Substitution with Elimination in a Dinitrosalicylic Lactone or Ester via Meisenheimer Intermediates

DOI: 10.1021/jo00365a031

Source and publish data:

Journal of Organic Chemistry p. 3016 - 3023 (1986)

Update date:2022-08-04

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Authors:

Jones, Paul R.

Rothenberger, Scott D.

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Article abstract of DOI:10.1021/jo00365a031

The dinitro lactone 1b and dinitro ester 2b derived from salicylic acid undergo S_NAr reactions in the presence of a variety of N-,O-, and S-nucleophiles.Substitution is accompanied by elimination of the β-ethylenoxy group, the ester group in no

Full text of DOI:10.1021/jo00365a031

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