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ChemInform Abstract: Synthesis of Novel Oxazolines and Application in Cyanosilylation of Prochiral Ketones.

✍ Scribed by Luo Mei; Li Xiao Xuan; Ke Yu Ping; Yin Hao; Hu Ke Liang; Zhang Jia Hai; Jiang Ying


Publisher
John Wiley and Sons
Year
2008
Weight
28 KB
Volume
39
Category
Article
ISSN
0931-7597

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πŸ“œ SIMILAR VOLUMES


Synthesis of novel oxazolines and applic
✍ Luo Mei; Li Xiao Xuan; Ke Yu Ping; Yin Hao; Hu Ke Liang; Zhang Jia Hai; Jiang Yi πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 206 KB

## Abstract A new family of oxazolines was synthesized in high yields and was characterized by NMR, IR, and MS. Oxazoline–lanthanide complexes, as the novel Lewis acid catalysts, were applied to the asymmetric cyanosilylation of ketones that gave the corresponding cyanohydrin trimethylsilyl ethers

Synthesis of novel oxazolines and applic
✍ Luo Mei; Li Xiao Xuan; Ke Yu Ping; Yin Hao; Hu Ke Liang; Zhang Jia Hai; Jiang Yi πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 34 KB

Table titled "The Cyanosilylation of Ketones Catalyzed by Rare Earth Complex 2c-La [10]" in column 2 of page 681 should be Table 4. The online version of this paper has been corrected.

ChemInform Abstract: Catalytic Enantiose
✍ Yoshitaka Hamashima; Motomu Kanai; Masakatsu Shibasaki πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 26 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

Synthesis of novel chiral Schiff bases a
✍ Zhongqiang Zhou; Yongjun Bian πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 100 KB

## Abstract Novel chiral Schiff bases were synthesized from (+)‐camphor, and their application to asymmetric transfer hydrogenation of prochiral ketones is described. The asymmetric transfer hydrogenation reaction could afford excellent conversion rates (up to 97.3%) and up to 27.3% enantiomeric ex