Photoaddition reactions of 3-nitro-2-enopyranoside derivatives in 1,3-dioxolane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference7 articles.
1. Stereochemistry of nucleophilic addition reactions 13
2. Photoreaction of methyl 4,6-O-benzylidene-2,3-dideoxy-3-nitro-β-d-erythro-hex-2-enopyranoside with 1,3-dioxolane and tetrahydrofuran
3. Selective Reduction of Carbohydrate Nitroolefins
4. 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
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1. Carbon Nitride Photoredox Catalysis Enables the Generation of the Dioxolanyl Radical for Conjugate Addition Reactions;ACS CATAL;2022
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3. C–H Activation via Radical Processes Using Photo-Excited Ketones;Topics in Heterocyclic Chemistry;2018
4. Alkylation of Nonacidic C(sp3)–H Bonds by Photoinduced Catalytic Michael-Type Radical Addition;Organic Letters;2016-09-26
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