A new type of carbonium ion rearrangement. Cyclization of 3,4-diphenylbut-3-en-2-one oxime benzoate to 1-phenyl-3-methylisoquinoline
✍ Scribed by Stefan Goszczyński; Ewa Salwińska
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 154 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
A/~trac~ A new type of anionic ¢yelization has been discovered in which the condensation of alkyl benzoates with simple nitriles, induced by an excess of LDA, leads directly to substituted-3-amino-2-indan-l-ones. The corresponding intermediL.t,~-[~-oxmitriles undergo cyclization to give, in most ins