๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Photochemical (2+2) cycloaddition of aromatic thiones to ketenimines. Acid catalyzed rearrangement of 2-iminothietanes

โœ Scribed by R.G. Visser; J.P.B. Baaij; A.C. Brouwer; H.J.T. Bos


Book ID
104235800
Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
141 KB
Volume
18
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Acid-catalyzed rearrangement of O-(2-ary
โœ Yasuyuki Endo; Ken-ichiro Kataoka; Naoki Haga; Koichi Shudo ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 235 KB

Acid-catalyzed rearrangement of 0-(2-arylphenyl)hydroxylamines followed by ring enlargement affords 7-aryl-2,3-dihydro-lH-azepin-2-ones. 2-Amino-2-phenyl-3,5-cyclohexadienone, an intermediate of the reaction, was trapped as the N-trifluoroacetamide.

Photochemical, acid, and base catalyzed
โœ D. Gravel; J. Gauthier ๐Ÿ“‚ Article ๐Ÿ“… 1968 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 317 KB

A recent communication by Schuster and Brizzolara (1) prompts us to report our results on the investigation of the photochemical rearrangement of 5,10-dimethyl-5-hydroxy-A lV9-2-octalone (1). In studying the photochemistry of compound 1, it was hoped that the presence of a hydroxyl group in an appro