Stereoselective synthesis of (3R,4S)-statine utilising the iron acetyl complex [(η5-C5H5)Fe(CO)(PPh3)COMe] as a chiral acetate enolate equivalent.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference54 articles.
1. PEPSTATIN, A NEW PEPSIN INHIBITOR PRODUCED BY AGTINOMYGETES
2. NEW PEPSTATINS, PEPSTATINS B AND G, AND PEPSTANONE A, PRODUCED BY STREPTOMYCES
3. SYNTHESIS OF 4-AMINO-3 HYDROXY-6-METHYLHEPTANOIG ACID, AN AMINE COMPONENT OF PEPSTATIN
4. ABSOLUTE CONFIGURATION OF 4-AMINO-3-HYDROXY-6-METHYLHEPTANOIC ACID PRESENT IN PEPSTATIN A AND STEREOSPECIFIC SYNTHESIS OF ALL FOUR ISOMERS
5. X-RAY STRUCTURE DETERMINATION OF 4-AMINO-3-HYDROXY-6-METHYLHEPTANOIC ACID, AN AMINE COMPONENT OF PEPSTATIN
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1. Stereoselective syntheses of substituted succinic acid derivatives of the iron chiral auxiliary [(η5-C5H5)Fe(CO)(PPh3)];Tetrahedron;2014-11
2. Addition To C=O Bonds II;Key Chiral Auxiliary Applications;2014
3. Diversity-Oriented Synthesis of Aminocyclohexitols from Garner's Aldehyde;Synthesis;2013-01-09
4. Stereochemical aspects of nucleophilic addition reactions to alkoxycarbene cations of the iron chiral auxiliary [(η5-C5H5)Fe(CO)(PPh3)];New Journal of Chemistry;2013
5. Progress in the Asymmetric Synthesis of Statine and Its Analogs;Chinese Journal of Organic Chemistry;2012
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