Stereochemistry of some “mixed hydride” reductions of 1-phenylcyclopentene oxide
✍ Scribed by Peter T. Lansbury; V.A. Pattison
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- French
- Weight
- 146 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Mixed hydride" reducing agents prepared from lithium aluminum hydride (l&i) and aluminum chloride in diethyl ether have been utilized by Eliel and coworkers (l-3) for the reduction of unsymmetrical epoxides, such as styrene oxide (1) and triphenylethylene oxide (2). Depending upon the ratios of
📜 SIMILAR VOLUMES
The reactions of hydrides and Grignard reagents with simple open-chain alaehydes aa ketones I (L, M, S, and R being groups containing carbon and hy- drogen only) are known to lead predominantly to the diastereoisomers IIA, as predicted by "Cram's rule" (1). I ## IIA IIB According to current theo
## Abstract The factors influencing the ease of the lithium aluminium hydride reduction of various 1,2‐epoxycycloalkanes and 1,2‐epoxyalkanes are described and discussed.