## Abstract The easily prepared and recoverable chiral __N__‐sulfonylated __β__‐amino alcohol **2** in combination with Ti(OPr‐__i__)~4~was found to be an effective chiral catalyst for the enantioselective addition of alkynylzinc to ketones, which gave the useful products, __i.e.__ chiral tertiary
Mechanism of Asymmetric Dialkylzinc Addition to Aldehydes Catalyzed by Titanium(IV) Complexes of N -Sulfonylated β-Amino Alcohols
✍ Scribed by Wu, Kuo-Hui; Gau, Han-Mou
- Book ID
- 126137031
- Publisher
- American Chemical Society
- Year
- 2004
- Tongue
- English
- Weight
- 211 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0276-7333
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📜 SIMILAR VOLUMES
A chiral (1R,2S)-2-(p-toluenesulfonylamino)-1,3-diphenyl-1-propanol derived catalyst was synthesized and successfully grafted onto amorphous silica gel and mesoporous silica (MCM-41) by a facile approach. This is the first use of silica-immobilized titanium(IV) complexes of N-sulfonylated amino alco
## Abstract An __N__‐sulfonylated β‐amino alcohol (__R__,__S__,__S__,__R__)‐**9** with four stereogenic centers is prepared. The titanium complex of **9** is an effective catalyst to induce excellent enantioselectivities for diethylzinc addition to aromatic aldehydes with ee values up to 99%. The f