Novel photocyclization of β,γ-unsaturated oximes
✍ Scribed by Diego Armesto; Ana Ramos; Maria J. Ortiz; Maria J. Mancheño; Elena P. Mayoral
- Book ID
- 104589793
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 313 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0165-0513
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## Abstract magnified image 3,5‐Disubstituted Δ^2^‐isoxazolines can be prepared using the palladium‐mediated nucleometalation / methoxycarbonylation of β,γ‐unsaturated oximes. This novel route to this class of compounds is tolerant of a wide variety of functionality in the starting material, and p
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
The photochemical SET induced cyclization of some fi,y-unsaturated oximes using 9, lo-dicyanoanthracene provides an efficient route for the synthesis of novel dihydroisoxazole derivatives.