## Summarv Reduction of cychc a-hydroxyketoxlmes with borane provides an excellent, high yleldmg, reglo-and stereoselectlve route to a-1,2-amlnoalcohols.
Electroreductive intermolecular coupling of ketones with O-methyl oximes. A convenient route to synthesis of 2-amino alcohols
β Scribed by Tatsuya Shono; Naoki Kise; Taku Fujimoto
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 243 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The electroreduction of ketones together with O-methyl oximes gave intermolecularly coupled products, 2-methoxyamino alcohols, which were easily reduced to 2-amino alcohols.
Reductive cross coupling of C=O group with C=N group will provide a convenient route to the synthesis of 2amino alcohols (eql). It has been reported that electroreductive coupling of N-methylbenzylideneaine with 'C' 'c' ::
π SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Aminobenzyl alcohol undergoes oxidative cyclization with aryl(alkyl), alkyl(alkyl) and cyclic ketones in dioxane at 80Β°in the presence of a catalytic amount of RhCl(PPh 3 ) 3 along with KOH to afford the corresponding quinolines in good yields. The catalytic pathway seems to be proceeded via a seque
1997 carboxylic acid derivatives carboxylic acid derivatives (naphthalene compounds) Q 0950 ## 25 -090 Efficient Synthesis of 1-Amino-2-naphthalenecarboxylic Acid Derivatives via a Sequential Michael Addition/Enolate-Nitrile Coupling Route and Its Application to Facile Preparation of 9-Amino Analo