N-Benzyloxymalimide for an easy access to 5-alkyl-3-pyrrolin-2-ones: asymmetric synthesis of the mixed imide substructure of the potent immunosuppressant microcolin B-Reference-Cited by-同舟云学术

N-Benzyloxymalimide for an easy access to 5-alkyl-3-pyrrolin-2-ones: asymmetric synthesis of the mixed imide substructure of the potent immunosuppressant microcolin B

Published:2010-04 Issue:8 Volume:21 Page:895-902
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Ye Zhao-Bao,Chen Jie,Meng Wei-Hua,Huang Pei-Qiang

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference84 articles.

1. Practical Asymmetric Approach to Pyrrolidinones: Efficient Synthesis of (+)-Preussin and (−)-AHPPA

2. Approach to the hyacinthacines: first non-chiral pool synthesis of (+)-hyacinthacine A1

3. Asymmetric synthesis of (+)-castanospermine through enol ether metathesis–hydroboration/oxidation

4. Diastereofacial selectivity in reduction of chiral tetramic acids

5. A facile synthesis of N-protected statine and analogs via a lipase-catalyzed kinetic resolution

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