A Route to C2-Methyl-hex-2-enopyranose Synthons
Author:
Affiliation:
1. b BASF AG , Farbenlaboratorium D-6700, Ludwigshafen, Germany
2. a Department of Chemistry, Paul M. Gross Chemical Laboratory , Duke University , Durham, North Carolina, 27708-0346, USA
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328309408011670
Reference14 articles.
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3. The 2- and 3-C-Methyl Derivatives of Methyl 2,3-Dideoxy-α-D-erythro-hex-2-enopyranosid-4-ulose
4. Synthetic studies relating to the C1–C9 “Eastern” Half of Rosaramicin
5. Revision of the assignment of relative stereochemistry in sibirosamine: synthesis of methyl n-tosyl α-d-disirosaminopyranoside
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1. ChemInform Abstract: A Route to C2-Methyl-hex-2-enopyranose Synthons.;ChemInform;2010-08-18
2. A practical and enantiospecific conversion of d-galactose to a substituted α,β-unsaturated δ-lactone synthon;Tetrahedron Letters;2007-12
3. An Unusual C-1C-2 Ring-Splitting of Pyranosides by a Retro-Aldol Reaction - a Route to New Chiral Building Blocks;Liebigs Annalen;2006-01-25
4. Cyclopropanation of glycals: Application to the synthesis of 2-deoxy-2-vinyl glycosides;Tetrahedron Letters;1995-12
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