𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Asymmetric reduction of ketoxime O-alkyl ethers with chirally modified NaBH4?ZrCl4

✍ Scribed by Itsuno, Shinichi; Sakurai, Yoshiki; Shimizu, Koji; Ito, Koichi


Book ID
118043902
Publisher
Royal Society of Chemistry
Year
1990
Weight
549 KB
Volume
7
Category
Article
ISSN
1472-7781

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Chirally Modified N
✍ K. Purushothama Chary; R. Mathew Thomas; D. S. Iyengar πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Asymmetric reduction of ketoxime ethers
✍ John T. Dougherty; Joseph R. Flisak; Jerome Hayes; Ivan Lantos; Li Liu; Lynn Tuc πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 English βš– 183 KB

The asymmetric reduction of ketoxime ethers to yield enantiomerically enriched chiral hydroxylamines with reagents prepared from borane and norephedrine has been investigated. Very high enantioselectivity (ca. 99% ee) was obtained in the reduction of ketoxime O-(o-nitrobenzyl) ether to O-(o-nitroben

ChemInform Abstract: Asymmetric Reductio
✍ J. T. DOUGHERTY; J. R. FLILSAK; J. HAYES; I. LANTOS; L. LIU; L. TUCKER πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 29 KB πŸ‘ 2 views

Asymmetric Reduction of Ketoxime Ethers to Optically Active O-Substituted Hydroxylamines with Reagents Prepared from Borane and Chiral Amino Alcohols. -The reduction in the presence of norephedrine is an efficient method to prepare chiral O-substituted hydroxylamines. However, O-Tbs and O-tBu subst