Urinary metabolites of 3a,4,5,6,7,7a-Hexahydro-3-(1-methyl-5-nitro-1H-imidazol-2-yl)-1,2-benzisoxazole in the dog
β Scribed by W. J. A. Vandenheuvel; B. H. Arison; T. W. Miller; P. Kulsa; P. Eskola; H. Mrozik; A. K. Miller; H. Skeggs; S. B. Zimmerman; B. M. Miller
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 328 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0022-3549
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π SIMILAR VOLUMES
## Abstract magnified image Oxidation of metronidazole (**4**) with sodium dichromate yielded the corresponding 2β(2βmethylβ5βnitroβ1__H__βimidazolβ1βyl)acetic acid (**5**) which was esterified with 1βbutanol to give butyl 2β(2βmethylβ5βnitroβ1__H__βimidazolβ1βyl)acetate (**8**). Reaction of the l
Hexahydro-4a-methyl-7,7-diphenyl-1(2H)-naphthalenone. -A clean and efficient route to the hitherto not reported title compound (VIII) starting from the known 3-ethenylcyclohexanone (I) is given. The approach represents a general strategy for the synthesis of related 7,7-diarylhexahydronaphthalenone