It has been reported that the reaction of halogenoazulenes with some nucleophilic reagents gave the corresponding substitution products by replacement of the halogen0 substituents with the reagents (1, 2, 3). However, no report has
The reaction of diethyl 2 chloro- and diethyl 2-methoxy-azulene-1,3-dicarboxylates with Grignard reagents
β Scribed by Noritaka Abe; Kahei Takase
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 231 KB
- Volume
- 14
- 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 βFull Textβ option. The original article is trackable v
The stereoelectronically controlled reaction of P-methoxy-1,3-dioxane (1) with Grignard reagents does not follow the course suggested by the behavior of anancomeric models for the conformational isomers of 1. Treatment of 1 with RMgX leads to the predominant formation of acid labile 3-(l'-methoxyalk