Creating Chiral Organoalanes and Organic Derivatives
- 總結
- Researchers at Purdue University have developed a method that uses Zr-catalyzed asymmetric carboalumination of alkenes to produce chiral alkylalanes. These chiral alkylalanes can then be converted to various chiral organic compounds, such as isoalkyl alcohols and other organic compounds of interest, which can then be used in the production of vitamins, pharmaceuticals, and other medicinally and biologically important compounds. This process also yields isoalkyl alcohols with a high enantiomeric excess (e.e.), often exceeding 95% e.e.
- 技術優勢
- Can be used in production of various organic compounds of interestYields isoalkyl alcohols with high enantiomeric excess
- 技術應用
- Chemical AnalysisPhamaceuticalsMedical/Healthcare
- 詳細技術說明
- Ei-ichi NegishiPurdue Chemistry
- *Abstract
-
- *Background
- Catalytic enantioselective carbon-carbon bond formation is a highly desirable but difficult synthetic task when it involves simple alkenes without heteroatom function groups.
- *IP Issue Date
- Dec 14, 1999
- *IP Type
- Utility
- *Stage of Development
- Process Validation in Lab
- *Web Links
- Purdue Office of Technology CommercializationPurdueInnovation and EntrepreneurshipEi-ichi NegishiPurdue Chemistry
- 國家
- United States
- 申請號碼
- 6,002,037
- 國家/地區
- 美國
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