Stereochemistry of Nucleophilic Addition Reactions. 10. Preparation of 2-C-Diacetylmethyl and 2-C-Acetylmethyl Derivatives with theAltro, Gluco, andMannoConfiguration from Methyl 4,6-O-Benzylidene-2,3-dideoxy-3-nitro-α-D-erythro-hex-2-enopyranoside
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/53/8/53_8_2322/_pdf
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1. Michael reactions on conformationally flexible methyl 3-C-nitro-hex-2-enopyranoside derivatives;Carbohydrate Research;2000-08
2. Photoaddition reactions of 3-nitro-2-enopyranoside derivatives in 1,3-dioxolane;Carbohydrate Research;1992-03
3. Formation of dihydrofuran derivatives by intramolecular substitution of the manno adducts formed by Michael reaction of a 1-O-acetyl-3-C-nitro-2-enopyranose derivative with 2,4-pentanedione and dibenzoylmethane;Carbohydrate Research;1991-06
4. Stereochemistry of nucleophilic addition reactions 13;Tetrahedron;1984-01
5. Reactions of methyl 4,6-O-benzylidene-2,3-dideoxy-3-nitro-α- and-β-d-erythro-hex-2-enopyranosides with phenylacetonitrile: Preparation and structural determination of adducts and an isoxazole derivative;Carbohydrate Research;1983-09
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