## Abstract The Friedel—Crafts reaction of aziridines (V) with arenes (VI) proceeds regioselectively to afford amino esters (VII), whilst the reaction with 1,4‐dimethoxybenzene (VIII) leads to an inseparable mixture of regioisomers (IX) and (X).
Friedel-Crafts Reactions of Vinylaziridine Linked to an Ester Group
✍ Scribed by Nagumo, Shinji; Takada, Hisashi; Yasui, Eiko; Sahara, Yui; Chinen, Yūki; Tanaka, Hirotoshi; Morita, Yusuke; Kobiki, Chihiro; Narisawa, Daiki; Mizukami, Megumi; Miyashita, Masaaki
- Book ID
- 118272862
- Publisher
- Japan Institute of Heterocyclic Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 814 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0385-5414
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📜 SIMILAR VOLUMES
Treatment of arylpropyl vinyloxiranes linked to ester with BF 3 was found to produce seven-membered ring products in excellent yields. This reaction proceeded in an inversion fashion.
Friedel-Crafts reactions of [arylthio(chloro)methyl]trimethylsilanes (ti,&) with arenes gave [aryl(arylthio)methyl]trimethylsilanes (a,b>, which were converted into arylmethyltrimethylsilanes (3) by reduction with Raney nickel. Arylmethyltrimethylsilanes (3) are versatile intermediates in organic sy