Applications of chiral allenylzinc additions and Noyori asymmetric reductions to an enantioselective synthesis of a C3–C13 precursor of the polyketide phosphatase inhibitor cytostatin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Cytostatin, a novel inhibitor of cell adhesion to components of extracellular matrix produced by Streptomyces sp. MJ654-NF4. I. Taxonomy, fermentation, isolation and biological activities.
2. Synthesis of the Protein Phosphatase 2A Inhibitor (4S,5S,6S,10S,11S,12S)-Cytostatin
3. Synthesis and biological evaluation of cytostatin analoguesElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b3/b305308n/
4. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
5. Addition of Allenylzinc Reagents, Prepared in Situ from Nonracemic Propargylic Mesylates, to Aldehydes. A New Synthesis of Highly Enantioenriched Homopropargylic Alcohols
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