Electroinduced oxidative transformation of 2,5-dioxabicyclo[4.4.0]decanes into 5-(1,3-dioxolan-2-yl)- and 5-(dimethoxymethyl)pentanoates
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference12 articles.
1. Electrooxidative rearrangement of 5,(n + 6)-dimethoxy-1-oxabicyclo[n.4.0]alkanes (n = 4, 10) into ω-(2-methoxytetrahydrofur-2-yl)alkanoic esters
2. Ring inversion barriers of 1,4-dioxane and cis-2,3-dimethyl-1,4-dioxane. Carbon-13 coupling-induced nonequivalence of vicinal protons
3. Synthese electrochimique de methoxy-2 dioxa-1,4 cyclanes par oxydation anodique de cetals cycliques de β-ceto-carboxylates
4. A Convenient Method for the Preparation of Bicyclic Dihydro-1,4-dioxins, Dihydro-1,4-oxathiins, Dihydro-1,4-dithiins and Related Compounds.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Electroinduced Oxidative Transformation of 2,5-Dioxabicyclo[4.4.0]decanes into 5-(1,3-Dioxolan-2-yl)- and 5-(Dimethoxymethyl)pentanoates.;ChemInform;2010-06-10
2. Electrochemical transformations of monooxa- and dioxabicycloalkenes and-bicycloalkanes;Russian Chemical Bulletin;1999-11
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