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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 52, 2022 - Issue 24
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Articles

Chemoselective benzylic oxidation of alkyl-substituted aromatics with singlet molecular oxygen generated from trans-3,5 hydroperoxy-3,5 dimethyl-1,2-dioxolan-3-yl ethaneperoxate

Zohreh NajminejadDepartment of Chemistry, Payame Noor University, Tehran, IranCorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0002-3676-3101View further author information
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Pages 2301-2310 | Received 05 Sep 2022, Published online: 11 Nov 2022

Citations (5)

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Read on this site (2)

Zohreh Najminejad. 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 0:0, pages 1-10.
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Z. Najminejad. 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 0:0, pages 1-8.
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Articles from other publishers (3)

Z Najminejad. (2024) 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 136:1.
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Z Najminejad & F Sameri. (2023) 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 135:3.
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R. Alan Aitken. 2023. 333 349 .

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