๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

cis-2-Amino-1-acenaphthenol: Practical resolution and application to the catalytic enantioselective reduction of ketones

โœ Scribed by Atsushi Sudo; Masaru Matsumoto; Yukihiko Hashimoto; Kazuhiko Saigo

Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
200 KB
Volume
6
Category
Article
ISSN
0957-4166

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

ChemInform Abstract: cis-1-Amino-1,2,3,4
ChemInform Abstract: cis-1-Amino-1,2,3,4-tetrahydro-2-naphthalenol: Resolution and Application to the Catalytic Enantioselective Reduction of Ketones.
โœ S. HIGASHIJIMA; H. ITOH; Y. SENDA; S. NAKANO ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 28 KB ๐Ÿ‘ 1 views

cis-1-Amino-1,2,3,4-tetrahydro-2-naphthalenol: Resolution and Application to the Catalytic Enantioselective Reduction of Ketones. -The optically active title amino alcohols are prepared by optical resolution of racemic amino alcohols with (-)-mandelic acid and used in the asymmetric reduction of ke

The chiral amino alcohol, cis-2-amino-1-
The chiral amino alcohol, cis-2-amino-1-acenaphthenol: Synthesis, resolution, and application to the diastereoselective [2,3]-Wittig rearrangement
โœ Atsushi Sudo; Yukihiko Hashimoto; Hiroki Kimoto; Kazuhiro Hayashi; Kazuhiko Saig ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 905 KB

The cbiral amino alcohol, cis-Zamino-1-acenaphthenol, was synthesized, and resolved by a simple procedure. This new chiral amino alcohol was converted into an oxaxoline derivative and applied as a chiral auxiliary to the diastereoselective (2.3]-Wittig rearrangement.

Suitably designed chiral amino alcohols:
Suitably designed chiral amino alcohols: synthesis, resolution and application to the catalytic enantioselective reduction of aryl alkyl ketones
โœ I. Reiners; J. Martens ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 301 KB

The amino alcohol rac-1-(1,2,3,4-tetrahydroisoquinoline-1-yl)-cyclopentanol was resolved via its O,O'-dibenzoyl-tartaric acid salt. These enantiomeric amino alcohols were used in the enantioselective reduction of prochiral aryl alkyl ketones. The resulting secondary alcohols were obtained in high en

cis-1-amino-2-indanol in asymmetric synt
cis-1-amino-2-indanol in asymmetric synthesis. Part I. A practical catalyst system for the enantioselective borane reduction of aromatic ketones
โœ Yaping Hong; Yun Gao; Xiaoyi Nie; Charles M. Zepp ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 278 KB

## A new class of oxozoboroltdine cotaIysts has been preporedjwn opticoliy pure cis-l-amino-2-indonols whtch ore ovoilable in loge quantities. The o~wnetric borone reduction of aromatic ketones using these catalysts has been studied.