Convenient synthesis of perinaphthane via chloroaluminum hydride reduction of perinaphthanone
β Scribed by Simpson, J. Ernest; Daub, Guido H.
- Book ID
- 126860566
- Publisher
- American Chemical Society
- Year
- 1979
- Tongue
- English
- Weight
- 157 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Hydride reduction of pyrrolo[1,4]benzodiazepine-5,lO-diones to carbinolamines is possible if a sufficiently electron-withdrawing group is present on the aromatic ring; the X-ray structure of one such product is given.
The recent findings that 2-oxazolines are inert to lithium aluminum hydride' and the successful implementation of a chiral non-racemic oxazoline as a reagent in asymmetric synthesis 2s3 have prompted a study involving oxazoline-hydrides as chiral reducing agents. Several chiral nonracemic oxazolines
## 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