## 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 βFull Textβ option. The original article is trackable v
Practical synthesis of chiral ligands for catalytic enantioselective cyanosilylation of ketones
β Scribed by Shuji Masumoto; Kazuo Yabu; Motomu Kanai; Masakatsu Shibasaki
- Book ID
- 104250873
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 72 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Ti(O i Pr) 4 + 1 or 2 (1 : 1) (1~10 mol %) + 71-92% 84-97% ee (R) 85-97% 62%-97 ee (S) Ln(O i Pr) 3 + 1 (1 : 2) (5~15 mol %) chiral ligands
π SIMILAR VOLUMES
## 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 βFull Textβ option. The original article is trackable v
Sterical and electronical tuning of the bifunctional catalyst 1 afforded the improved catalyst 2, which promoted the cyanosilylation of ketones with higher enantioselectivity as well as with improved catalyst turn-over with a factor of up to 10. Thus, chiral quaternary a-hydroxynitriles were obtaine
Enantioselective catalyst efficiency for the synthesis of the camptothecin family was improved through ligand-tuning. Key intermediates of two convergent syntheses of camptothecin (Curran's intermediate and Corey's intermediate) were obtained in up to 10 g scale through the catalytic enantioselectiv