Studies on an unexpected reaction involving a reductive cleavage of the pyridazine moiety of a tricyclic heterocycle are described. Structure assignments for the products obtained from the reductive cleavage were made using physicochemical methods. The pro drug' (TCN-P, fi) of 6-amino-4-N-methyl-8-(
β¦ LIBER β¦
The acid catalyzed ring opening of 1-oxaspiro[2.6]nonane. A 1,5 hydrogen shift.
β Scribed by L.H. Schwartz; M. Feil; A.J. Kascheres; K. Kaufmann; A.M. Levine
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 246 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
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