Claisen Rearrangements of 5,6-Dideoxy-1,2-O-isopropylidene-α-D-xylo- and α-D-ribo-hept-5-eno-1,4-furanoses with Triethyl Orthoacetate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/62/12/62_12_3978/_pdf
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2. Ortho ester Claisen rearrangements of three 3-C-(hydroxymethyl)methylene derivatives of hexofuranose: stereoselective introduction of a quaternary center on C-3 of D-ribo-, L-lyxo-, and D-arabino-hexofuranoses
3. Claisen rearrangement of (Z)-3-deoxy-3-C-[(hydroxymethyl)methylene]-1,2:5,6-di-O-isopropylidene-.alpha.-D-ribo-hexofuranose with triethyl orthopropionate
4. Stereoselective synthesis of the bis(tetrahydrofuran) moiety (C-1 to C-9) of (+)-asteltoxin, a novel mycotoxin from aspergillus stellatus
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