Epimerization of C5 of an N-hydroxypyrrolidine in the synthesis of swainsonine related iminosugars.

نویسندگان

  • Bao-Chen Qian
  • Akiko Kamori
  • Kyoko Kinami
  • Atsushi Kato
  • Yi-Xian Li
  • George W J Fleet
  • Chu-Yi Yu
چکیده

Epimerization of C5 of an N-hydroxypyrrolidine ring by regioselective oxidation to a nitrone followed by diastereoselective reduction provides a new approach to the synthesis of swainsonine and related compounds. The only protection in the synthesis of the potent mannosidase inhibitor DIM (1,4-dideoxy-1,4-imino-d-mannitol) was the acetonation of d-mannose.

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

Modeling and Optimization of Fixed-Bed Fischer-Tropsch Synthesis Using Genetic Algorithm

  In this paper, modeling and optimization of Fischer-Tropsch Synthesis is considered in a fixed-bed catalytic reactor using an industrial Fe-Cu-K catalyst. A one dimensional pseudo-homogenous plug flow model without axial dispersion is developed for converting syngas to heavy hydrocarbons. The effects of temperature, pressure, H2 to CO ratio in feed stream, and CO molar flow on the mass flow r...

متن کامل

Azetidine- and N-carboxylic azetidine-iminosugars as amyloglucosidase inhibitors: synthesis, glycosidase inhibitory activity and molecular docking studies.

A simple strategy for the synthesis of hitherto unknown azetidine iminosugars 2a–2c and N-carboxylic azetidine iminosugar 2d has been reported. The methodology involves the conversion of 1,2:5,6-di-O-isopropylidene-3-oxo-α-D-glucofuranose 3 to 3-azido-3-deoxy-3-C-(formyl)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 5 using the Jocic–Reeve and Corey–Link approaches. Compound 5 was transformed ...

متن کامل

Synthesis of highly epimerizable N-protected -amino aldehydes of high enantiomeric excess

The Dess–Martin periodinane was found to be a superior oxidant for the efficient, epimerization-free synthesis of optically active N-protected -amino aldehydes from the corresponding N-protected -amino alcohols. Highly racemization-prone products, including N-Fmoc phenylglycinal and N-trifluoroacetyl -amino aldehydes, were prepared in 95% yield with 1% epimerization. © 2000 Elsevier Science Ltd...

متن کامل

Synthesis of N-dialkylphosphoryl iminosugar derivatives and their immunosuppressive activities.

Twelve novel N-dialkylphosphoryliminosugar derivatives were synthesized and their immunosuppressive activities were evaluated on the proliferation of the mouse splenocytes and the secretion of IFN-γ and IL-4. The experimental data demonstrated that the iminosugars with the double long alkyl chains exhibited better inhibitory effects than those with the single long alkyl chain, and the iminosuga...

متن کامل

Direct synthesis of imino-C-nucleoside analogues and other biologically active iminosugars

Iminosugars have attracted increasing attention as chemical probes, chaperones and leads for drug discovery. Despite several clinical successes, their de novo synthesis remains a significant challenge that also limits their integration with modern high-throughput screening technologies. Herein, we describe a unique synthetic strategy that converts a wide range of acetaldehyde derivatives into i...

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:
  • Organic & biomolecular chemistry

دوره 14 19  شماره 

صفحات  -

تاریخ انتشار 2016