Synthetic studies on ambruticin: Determination of the absolute stereochemistry by a chiral synthesis of the cyclopropane ring
โ Scribed by Nigel J. Barnes; Alan H. Davidson; Leslie R. Hughes; Garry Procter; Veedianand Rajcoomar
- Book ID
- 104241625
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 200 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract The absolute configuration of the antibiotic (+)โxanthocidin (4,5โdihydroxyโ5โisopropylโ4โmethylโ2โmethyleneโ3โoxocyclopentaneโ1โcarboxylicacid, 1) was shown to be 1__R__,4__S__,5__S__ by the synthesis of its enantiomers. Lipase AK (Amano) was used for the key resolution step, and the a
A photooxygenation reaction of 2',2',4',4'-tetramethyl tetrahydroindole (9) followed by a pinacoltype rearrangement furnished 2',2 ',4',4'-tetramethyl-3-spirocydopentylsuccinimide (11). This transformation constitutes a model study for the synthesis of the spirosuccinimide ring system of asperparali
## 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 โFull Textโ option. The original article is trackable v