Mechanism of the Stevens Rearrangement of Ammonium Ylides. -The title rearrangement of the ylide precursor (I) is studied, revealing that the Stevens rearrangement occurs at room temperature. The isomerization to compound (II) is always accompanied by formation of the Sommelet-Hauser rearrangement p
β¦ LIBER β¦
ChemInform Abstract: The Controversial Reaction Mechanism of Stevens Rearrangement
β Scribed by Soumendranath Bhakat
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 18 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Review: 25 refs.
π SIMILAR VOLUMES
ChemInform Abstract: Mechanism of the St
β
Y. MAEDA; Y. SATO
π
Article
π
2010
π
John Wiley and Sons
β 26 KB
π 1 views
On the Mechanism of the Stevens Rearrang
β
Dr. E. F. Jenny; Dr. J. Druey
π
Article
π
1962
π
John Wiley and Sons
π
English
β 215 KB
π 2 views
ChemInform Abstract: Photo-Stevens Rearr
β
H. MORITA; H. KAMIYAMA; M. KYOTANI; T. FUJII; T. YOSHIMURA; S. ONO; C. SHIMASAKI
π
Article
π
2010
π
John Wiley and Sons
β 28 KB
ChemInform Abstract: The JacobsenβKatsuk
β
T. LINKER
π
Article
π
2010
π
John Wiley and Sons
β 25 KB
Borate Complexes Derived from Lithium Ca
β
Doz. Dr. G. KΓΆbrich; Dipl.-Chem. H. R. Merkle
π
Article
π
1967
π
John Wiley and Sons
π
English
β 103 KB
π 2 views
ChemInform Abstract: Mechanism of the Re
β
S. KOHMOTO; N. NAKAYAMA; J. TAKAMI; K. KISHIKAWA; M. YAMAMOTO; K. YAMADA
π
Article
π
2010
π
John Wiley and Sons
β 25 KB
Mechanism of the Rearrangement of 7-Vinylnorcaradienes. -Thermal rearrangement of the diastereomeric 7-vinylnorcaradienes (I) and (II) provides three products, two formed via a 1,3-and 3,5-vinylcyclopropanecyclopentane rearrangement and the third one resulting from a 3,3-cope rearrangement.