𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Synthesis of 1,4-Diketones by Michael Addition of O- Aroylmandelonitriles Involving Rearrangement of Aroyl Group and Decyanation.

✍ Scribed by A. MIYASHITA; Y. MATSUOKA; A. NUMATA; T. HIGASHINO


Book ID
112035274
Publisher
John Wiley and Sons
Year
2010
Weight
30 KB
Volume
27
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Olefin-Insertion Re
✍ A. MIYASHITA; A. NUMATA; Y. SUZUKI; K. IWAMOTO; T. HIGASHINO πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 30 KB πŸ‘ 1 views

Olefin-Insertion Reaction Between the Carbonyls of Benzils; Formation of 1,4-Diketones by Michael Addition Catalyzed by Cyanide Ion. -A novel Michael addition type olefination-insertion reaction between the carbonyl groups of benzils (I) affording 1,4-diketones (III) is described. Cyanide ion is req

ChemInform Abstract: Tandem Michael Addi
✍ Deepika Malhotra; Le-Ping Liu; Gerald B. Hammond πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 38 KB πŸ‘ 2 views

## Abstract The reaction leads to the 2‐alkynyl‐1,5‐diketones (III), when catalyzed by Bu~4~NF in THF at room temperature.