Additive-free aerobic oxidative difunctionalization of alkenes with P<sub>4</sub>S<sub>10</sub> and alcohols to access β-hydroxy phosphorodithioates-Reference-Cited by-同舟云学术

Additive-free aerobic oxidative difunctionalization of alkenes with P₄S₁₀ and alcohols to access β-hydroxy phosphorodithioates

Published:2023 Issue:24 Volume:25 Page:10678-10683
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Qu Chengming¹²,Lv Yufen²,Huang Jian²,Ma Chao²,Yue Huilan¹^ORCID,Wei Wei¹²^ORCID,Yi Dong³^ORCID

Affiliation:

1. Qinghai Provincial Key Laboratory of Tibetan Medicine Research and CAS Key Laboratory of Tibetan Medicine Research, Northwest Institute of Plateau Biology, Xining 810008, Qinghai, P. R. China

2. School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, Shandong, P. R. China

3. School of Pharmacy, Southwest Medical University, Luzhou 646000, Sichuan, P. R. China

Abstract

An efficient strategy has been established for the synthesis of β-hydroxy phosphorodithioates and alkyl phosphorodithioates via additive-free aerobic oxidative difunctionalization of alkenes with P4S10 and alcohols at room temperature.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/GC/D3GC02665E

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3. Synthesis, Properties, and Applications of Oligonucleotides Containing an RNA Dinucleotide Phosphorothiolate Linkage

4. A Berzelius Reagent, Phosphorus Decasulfide (P4S10), in Organic Syntheses

5. Design, synthesis and biological evaluation of organophosphorous-homodimers as dual binding site acetylcholinesterase inhibitors

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