Facile Rearrangement of O -Silylated Oximes on Reduction with Boron Trifluoride/Borane
✍ Scribed by Ortiz-Marciales, Margarita; Rivera, Luis D.; De Jesús, Melvin; Espinosa, Sandraliz; Benjamin, Josúe A.; Casanova, Orlando E.; Figueroa, Irving G.; Rodríguez, Sheila; Correa, Wilbert
- Book ID
- 127000217
- Publisher
- American Chemical Society
- Year
- 2005
- Tongue
- English
- Weight
- 93 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0022-3263
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📜 SIMILAR VOLUMES
4-Methoxy acetophenone oximes substituted at the oxygen with TMS, TBS, TIPS and MDPS groups were reduced with borane±THF obtaining the 4-methoxy-N-ethyl aniline as the principal product, up to a 95% yield in the case of the more hindered TIPS group. The 2-methoxy-and 2,4-methoxyacetophenone O-TBS ox
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