𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Rearrangement of Oxaspiroheptanes to Cyclohexanones Mediated by Lithium Iodide.

✍ Scribed by Didier Bouyssi; Marcello Cavicchioli; Sylvie Large; Nuno Monteiro; Genevieve Balme

Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
31
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Stereochemistry of
ChemInform Abstract: Stereochemistry of Enantioselective Deprotonation of 4-Substituted Cyclohexanones by Chiral Bidentate Lithium Amides.
✍ M. TORIYAMA; K. SUGASAWA; M. SHINDO; N. TOKUTAKE; K. KOGA πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 30 KB πŸ‘ 2 views

## Stereochemistry of Enantioselective Deprotonation of 4-Substituted Cyclohexanones by Chiral Bidentate Lithium Amides. -Enantioselective deprotonation of 4-substituted cyclohexanones using chiral lithium amide bases such as (I) in the presence of excess trimethylsilyl chloride results in format

ChemInform Abstract: Palladium-Catalyzed
ChemInform Abstract: Palladium-Catalyzed [1,3]-O-to-C Rearrangement of Pyrans Toward Functionalized Cyclohexanones.
✍ Julien C. R. Brioche; Thomas A. Barker; David J. Whatrup; Michael D. Barker; Jos πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 2 views

## Abstract Rearrangement of the pyran‐based aryl enol ethers proceeds with nearly complete diastereoselectivity affording the (E)‐trans products, regardless whether (E)‐ or (Z)‐substrates are being used.