Author:
Azarifar Davood,Khosravi Kaveh,Najminejad Zohreh,Soleimani Khadijeh
Publisher
Springer Science and Business Media LLC
Cited by
16 articles.
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1. Convenient transformation of thioamides and thioketones to their oxygen analogues with singlet oxygen generated from trans-5-hydroperoxy-3,5-dimethyl-1,2-dioxolan-3-yl ethaneperoxate;Journal of Sulfur Chemistry;2024-04-08
2. Oxidative decarboxylation of arylacetic acids and arylacetic esters with singlet molecular oxygen generated from trans-5-hydroperoxy-3,5-dimethyl-1,2-dioxolan-3-yl ethaneperoxate;Journal of Chemical Sciences;2024-02-12
3. Oxidative Cleavage of C=N Bond of Ketoximes with Singlet Molecular Oxygen Generated from
trans-
5-Hydroperoxy-3,5-dimethyl-1,2-dioxolane-3-yl Ethaneperoxoate;Organic Preparations and Procedures International;2024-02-05
4. C–N bond cleavage of benzylamines with singlet molecular oxygen generated from trans-5-hydroperoxy-3,5dimethyl-1,2-dioxolan-3-yl ethaneperoxate: synthesis of 2,4,6-triaryl pyridines;Journal of Chemical Sciences;2023-07-24
5. Oxidative Bromination of Unreactive Aromatic Substrates Promoted by trans-3,5-Dihydroperoxy-3,5-dimethyl-1,2-dioxolane in Water under Mild Conditions;Organic Preparations and Procedures International;2023-06-27