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Structure of the reduction products ofN-(m-tolyl)-exo-2,3-epoxybicyclo[2.2.1]heptane-endo-5,endo-6-dicarboximide with lithium tetrahydridoaluminate

✍ Scribed by L. I. Kas’yan; O. V. Krishchik; A. O. Kas’yan; I. N. Tarabara

Book ID
106523350
Publisher
SP MAIK Nauka/Interperiodica
Year
2004
Tongue
English
Weight
45 KB
Volume
40
Category
Article
ISSN
1070-4280

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Azabrendanes. III. Synthesis of stereoisomeric exo- and endo-5-acylaminomethyl-exo-2,3-epoxybicyclo[2.2.1]heptanes and their reduction by lithium aluminum hydride
✍ Lilija I. Kasyan; Igor N. Tarabara; Oxana A. Savel'yeva; Andrey O. Kasyan 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 121 KB

## Abstract A number of stereoisomeric N‐[aryl(alkyl, cycloalkyl)carbonyl]‐exo(endo)‐5‐aminomethylbicyclo[2.2.1]hept‐2‐enes have been synthesized from bicyclo[2.2.1]hept‐2‐en‐exo(endo)‐5‐carbonitrile via reduction of the latter by lithium aluminum hydride and subsequent reactions of the resulting a