𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reactions of 1,1,3,3-tetramethylindane-2-selone with grignard and organolithium reagents

✍ Scribed by Renji Okazaki; Akihiko Ishii; Naoki Inamoto


Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
172 KB
Volume
25
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


The title reaction afforded selenophilic, carbophilic, and reduction products depending on the kinds of the organometallic reagents and the heterophilic nature of the reaction was more conspicuous in the reaction with the selenoketone than with the corresponding thioketone.


πŸ“œ SIMILAR VOLUMES


Reactions of Grignard Reagents with 1,3-
✍ I. A. Novakov; B. S. Orlinson; E. N. Savel'ev; V. N. Urazbaev; Yu. B. Monakov πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons βš– 69 KB πŸ‘ 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Reaction of 2-methoxy-1,3-dioxane with g
✍ William F. Bailey; Allan A Croteau πŸ“‚ Article πŸ“… 1981 πŸ› Elsevier Science 🌐 French βš– 283 KB

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

The reaction of diethyl azulene-1,3-dica
✍ Noritaka Abe; Tadayoshi Morita; Kahei Takase πŸ“‚ Article πŸ“… 1973 πŸ› Elsevier Science 🌐 French βš– 194 KB

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