๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Stereoselective thermal rearrangements of 2-phenyl-alkenylidenecyclopropanes

โœ Scribed by Timothy B. Patrick; Edward C. Haynie; William J. Probst

Publisher
Elsevier Science
Year
1971
Tongue
French
Weight
96 KB
Volume
12
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Stereoselectivities in AgBF4-catalyzed a
Stereoselectivities in AgBF4-catalyzed and photoinduced phenyl-rearrangement of 2-chloropropiophenone
โœ Satoshi Usui; Takeshi Matsumoto; Katsutoshi Ohkubo ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 240 KB

S)-2-Phenylpropionic acid was stereoselectively obtained by the AgBF 4catalyzed phenyl-rearrangement of (S)-2-chloropropiophenone dimethyl acetal, while the photoirradiafion of (S)-or (R)-2-chloropropiophenone afforded partially racemized (S)or (R)-2-phenylpropionic acid, respectively. An intramolec

Beckmann rearrangement of 3-phenyl-2-iso
Beckmann rearrangement of 3-phenyl-2-isoxazolines
โœ G. Cainelli; S. Morrocchi; A. Quilico ๐Ÿ“‚ Article ๐Ÿ“… 1963 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 274 KB

2-Isoxazolines may be regarded as cyclic ethers of S-ketol oximes, although ring I is remarkably stable towards hydrolytic agents. Since it is known that oxime ethers may undergo the Beckmaan rearrangement, it was considered probable that under suitable conditions 2-isoxazolines should also give thi