Synthesis of the THF Moiety of Annonacin Based on Aldolization and Baeyer-Villiger Oxidation. -Anti-aldolization of cyclohexanone with γ,δ-unsaturated aldehydes followed by epoxidation-cyclization and stereoselective Baeyer-Villiger oxidation provides a new and simple approach to key-THF synthons o
✦ LIBER ✦
Synthesis of the THF moiety of annonacin based on aldolisation and Baeyer-Villiger oxidation
✍ Scribed by Jean-Pierre Gesson; Brigitte Renoux; Els Schulten
- Book ID
- 104257646
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 194 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
ChemInform Abstract: Synthesis of the TH
✍
J.-P. GESSON; B. RENOUX; E. SCHULTEN
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 32 KB
👁 2 views
Sodium Perborate—A Convenient Baeyer–Vil
✍
Maria Espiritu; Paul N. Handley; Ralf Neumann
📂
Article
📅
2003
🏛
John Wiley and Sons
🌐
English
⚖ 50 KB
👁 1 views
ChemInform Abstract: Synthesis of Spiroc
✍
J. COSSY; B. GILLE; V. BELLOSTA
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 34 KB
👁 2 views
ChemInform Abstract: Synthesis of Chiral
✍
Ayhan S. Demir; Asuman Aybey
📂
Article
📅
2009
🏛
John Wiley and Sons
⚖ 55 KB
👁 2 views
Bioreduction of (R)-carvone and regiosel
✍
David L. Varie; John Brennan; Barbara Briggs; Jason S. Cronin; David A. Hay; Joh
📂
Article
📅
1998
🏛
Elsevier Science
🌐
French
⚖ 276 KB
A theoretical study on the mechanism of
✍
Attila Kovács; Dénes S. Nemcsok; György Keglevich
📂
Article
📅
2007
🏛
John Wiley and Sons
🌐
English
⚖ 444 KB
## Abstract DFT computations have been performed on selected stationary points of the reaction path (reactants, intermediates, and products) of the Baeyer–Villiger type oxidation of 7‐phosphanorbornene 7‐oxide derivatives. Our computations justified the relevance of a Criegee‐type intermediate form