Stereochemical Studies on 1,6 Additions to 10-Methyl-1(9),7-hexal-2-one by Grignard Reagents
โ Scribed by Marshall, James A.; Roebke, Heide
- Book ID
- 127184275
- Publisher
- American Chemical Society
- Year
- 1966
- Tongue
- English
- Weight
- 751 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Conjugate additions of Zithiated arylacetonitriles to 2-octaZones give good yields of cis-decalone products. Z'he stereochemistry of the adducts is determined by 13 C NMR spectroscopy. Conjugate additions of enolates2, 3 4 cuprates , allylsilanes and aluminum or zirconium acetylides (via nick
1998 structure structure (organic substances) K 9000 46 -031 9-Methyl-8,11,12-trioxatricyclo [7.2.1.O 2,7 ]dodeca-2,4,6-trien-10-one. -The structure of the title compound (I), unexpected reaction product of salicylaldehyde and pyruvic acid, is elucidated by X-ray diffraction analysis. -(EILERS, F.;