Intramolecular aldol condensation applied to -glucose-derived δ-ketoaldehydes : access to enantiomerically pure six-membered carbocycles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. A NOVEL SYNTHESIS OF PSEUDO-α-L-ALTROPYRANOSE FROM D-GLUCOSE
2. Construction of an Optically Active 7-Oxabicyclo[4.3.0]non-4-en-3-one Skeleton from D-Glucose, and Its Transformation to Some Pseudo-Hexopyranoses
3. Construction of an enantiomerically pure cis-fused 7-oxabicyclo[4.3.0]nonan-3-one skeleton. Synthesis of (1S,6R,8R,9R)-8,9-(isopropylidenedioxy)-7-oxabicyclo[4.3.0]nonan-3-one from D-allose
4. Syntheses of Optically Active Pentaacetates of Pseudo-β-L-allopyranose and Pseudo-α-D-mannopyranose
5. Pd(II)-mediated intramolecular acetal formation applied to a substrate prepared from D-glucose : A formal synthesis of enantiomeric paniculide B
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2. Challenges to the Synthesis of Structurally Unique Cyclic Skeletons and Application to Biologically Intriguing Natural Product Synthesis;Journal of Synthetic Organic Chemistry, Japan;2011
3. ChemInform Abstract: Intramolecular Aldol Condensation Applied to D-Glucose-Derived δ- Ketoaldehydes: Access to Enantiomerically Pure Six-Membered Carbocycles.;ChemInform;2010-08-21
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5. 1-Aza-sugars from d -glucose. Preparation of 1-deoxy-5-dehydroxymethyl-nojirimycin, its analogues and evaluation of glycosidase inhibitory activity;Bioorganic & Medicinal Chemistry;2002-07
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