Chiral chromatography in support of pharmaceutical process research

نویسنده

  • CHRISTOPHER J. WELCH
چکیده

Preparative chiral chromatography has recently become a preferred method for rapidly accessing enantiopure compounds in the pharmaceutical industry [1–8]. While preparative chromatographic enantioseparation has been practiced for a number of years by specialized researchers, the current widespread interest in the approach can be attributed in part to advances in equipment and stationary phases, but more importantly, to an increasingly widespread realization of the cost-effectiveness of this technique. In many instances, developing and executing a chromatographic enantioseparation is faster and less labour-intensive than more traditional approaches for accessing enantiopurity. Consequently, preparative chiral chromatography is increasingly used in place of, or in conjunction with, the more traditional methods of organic synthesis. We herein present a general introduction that focuses on some of the current areas of interest in the field of preparative chromatographic enantioseparation, which we hope will be useful to newcomers and experienced practitioners alike.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Chiral recognition mechanisms of four β-blockers by HPLC with Amylose Chiral Stationary Phase

The high performance liquid chromatography (HPLC) enantioseparation of four β-blocking agents metoprolol, bisoprolol, propranolol and atenolol was performed on amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase using n-hexane-ethanol-diethylamine (DEA) as the mobile phase and related chiral recognition mechanisms were discussed. Enantiomeric separation of the fourβ-blockers was ...

متن کامل

Chiral recognition mechanisms of four β-blockers by HPLC with Amylose Chiral Stationary Phase

The high performance liquid chromatography (HPLC) enantioseparation of four β-blocking agents metoprolol, bisoprolol, propranolol and atenolol was performed on amylose tris-(3,5-dimethylphenylcarbamate) chiral stationary phase using n-hexane-ethanol-diethylamine (DEA) as the mobile phase and related chiral recognition mechanisms were discussed. Enantiomeric separation of the fourβ-blockers was ...

متن کامل

Development of a new method based on chiral ligand-exchange chromatography for the enantioseparation of propranolol

A new chromatographic procedure was proposed for the separation of propranolol (PRN) enantiomers based upon enantioselective chiral ligand-exchange chromatography. The separation was carried out on a short C8 column leading to considerably short separation time. L-alanine and Cu2+ were applied as chiral selector and central bivalent complexing ion, respectively. It was found that the kind of co...

متن کامل

Development of a new method based on chiral ligand-exchange chromatography for the enantioseparation of propranolol

A new chromatographic procedure was proposed for the separation of propranolol (PRN) enantiomers based upon enantioselective chiral ligand-exchange chromatography. The separation was carried out on a short C8 column leading to considerably short separation time. L-alanine and Cu2+ were applied as chiral selector and central bivalent complexing ion, respectively. It was found that the kind of co...

متن کامل

Review High-performance liquid chromatographic enantioseparation of drugs containing multiple chiral centers on chiral stationary phases

In recent years there has been considerable interest in the synthesis and separation of enantiomers of organic compounds especially because of their importance in the biochemistry and pharmaceutical industry. High-performance liquid Chromatography is a very useful method for the direct separation of enantiomers. However, about 30−40 years ago, commercially available chiral stationary phases wer...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2004