Molecular rearrangements in organic synthesis /
Uloženo v:
| Další autoři: | |
|---|---|
| Typ dokumentu: | Kniha |
| Jazyk: | Angličtina |
| Vydáno: |
Hoboken, NJ :
Wiley,
[2015]
|
| Témata: | |
| On-line přístup: | Elektronická verze přístupná pouze pro studenty a pracovníky MU |
| Příbuzné jednotky: | Tištěná verze::
Molecular rearrangements in organic synthesis. |
Obsah:
- 1,2-migrations. Pinacol and semi-pinacol rearrangements in total synthesis
- Baeyer-Villiger (BV) oxidation/rearrangement in organic synthesis
- The Wolff rearrangement : tactics, strategies and recent applications in organic synthesis
- Alkyl and acyl azide rearrangements
- Beckmann rearrangements and fragmentations in organic synthesis
- Brook rearrangement. 1,2-migrations via three-membered rings. The quasi-favorskii rearrangement
- The Ramberg-Backlund reaction
- Applications of di-pi-methane and related rearrangement reactions in chemical synthesis. 1,3-transpositions. Payne rearrangement
- Vinylcyclopropane-cyclopentene rearrangement
- Ferrier carbocyclization reaction. [3,3]- and [2,3]-sigmatropic rearrangements. The Claisen rearrangement
- [3,3]-sigmatropic rearrangements with heteroatom-heteroatom bonds
- [2,3]-rearrangements of ammonium zwitterions
- Oxonium ylide rearrangements in synthesis
- The [2,3]-Wittig rearrangement
- The Mislow-Evans rearrangement. Ipso rearrangements. Smiles rearrangements
- Pummerer-type reactions as powerful tools in organic synthesis.