Metal-free catalytic nucleophilic substitution of primary alcohols with secondary phosphine oxides

The first dehydrative version of the Michaelis–Arbuzov reaction was developed, and two possible dehydration pathways were proposed.

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Publication Details

Journal
Green Chemistry
Published
2024-11-27
DOI
https://doi.org/10.1039/d4gc04409f
Citations
10
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
1.58
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article

Metal-free catalytic nucleophilic substitution of primary alcohols with secondary phosphine oxides

Xiantao Ma, Li‐Biao Han, Jiarui Guo, Ran Yan et al.
10 citations
Green Chemistry
Asymmetric Hydrogenation and Catalysis
1.58
article

Metal-free catalytic nucleophilic substitution of primary alcohols with secondary phosphine oxides

Xiantao Ma, Li‐Biao Han, Jiarui Guo, Ran Yan, Jing Yu, Qing Xu, Jun Jie Bian, Xiaoyu Yan
article en
10 citations

Abstract

The first dehydrative version of the Michaelis–Arbuzov reaction was developed, and two possible dehydration pathways were proposed.

Green ChemistryVol. 27(1)
Xinyang Normal University (CN), Wenzhou University (CN), Shaoxing University (CN), Institute of New Materials (CN)
Clean water and sanitation
Openalex Percentile: Top 18%
Asymmetric Hydrogenation and Catalysis
1.58
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Metal-free catalytic nucleophilic substitution of primary alcohols with secondary phosphine oxides — Xiantao Ma, Li‐Biao Han, et al. · Green Chemistry (2024) | TGRS Research Map | TGRS