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author:

Ru, T. (Ru, T..) [1] | Zhang, Y. (Zhang, Y..) [2] | Wei, Q. (Wei, Q..) [3] | Zuo, S. (Zuo, S..) [4] | Jia, Z. (Jia, Z..) [5] | Chen, F.-E. (Chen, F.-E..) [6]

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Scopus

Abstract:

Hydroformylation of olefins is widely used in the chemical industry due to its versatility and the ability to produce valuable aldehydes with 100% atom economy. Herein, a hybrid phosphate promoter was found to efficiently promote rhodium-catalyzed hydroformylation of styrenes under remarkably mild conditions with high regioselectivities. Preliminary mechanistic studies revealed that the weak coordination between the Rhodium and the P=O double bond of this pentavalent phosphate likely induced exceptional reactivity and high ratios of branched aldehydes to linear products.

Keyword:

branched selectivity hybrid phosphate hydroformylation styrene

Community:

  • [ 1 ] [Ru T.]Department of Medicinal Chemistry, School of Pharmacy, Fudan University, 201203, Shanghai, China
  • [ 2 ] [Ru T.]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, 200433, Shanghai, China
  • [ 3 ] [Ru T.]Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, 200433, Shanghai, China
  • [ 4 ] [Zhang Y.]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, 200433, Shanghai, China
  • [ 5 ] [Zhang Y.]Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, 200433, Shanghai, China
  • [ 6 ] [Zhang Y.]College of Chemical Engineering, Fuzhou University, Fuzhou 350102, China
  • [ 7 ] [Wei Q.]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, 200433, Shanghai, China
  • [ 8 ] [Wei Q.]Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, 200433, Shanghai, China
  • [ 9 ] [Wei Q.]College of Chemical Engineering, Fuzhou University, Fuzhou 350102, China
  • [ 10 ] [Zuo S.]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, 200433, Shanghai, China
  • [ 11 ] [Zuo S.]Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, 200433, Shanghai, China
  • [ 12 ] [Jia Z.]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, 200433, Shanghai, China
  • [ 13 ] [Jia Z.]Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, 200433, Shanghai, China
  • [ 14 ] [Chen F.-E.]Department of Medicinal Chemistry, School of Pharmacy, Fudan University, 201203, Shanghai, China
  • [ 15 ] [Chen F.-E.]Engineering Center of Catalysis and Synthesis for Chiral Molecules, Department of Chemistry, Fudan University, 200433, Shanghai, China
  • [ 16 ] [Chen F.-E.]Shanghai Engineering Center of Industrial Asymmetric Catalysis for Chiral Drugs, 200433, Shanghai, China
  • [ 17 ] [Chen F.-E.]College of Chemical Engineering, Fuzhou University, Fuzhou 350102, China

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Source :

Molecules (Basel, Switzerland)

ISSN: 1420-3049

Year: 2024

Issue: 9

Volume: 29

3 . 0 6 0

JCR@2018

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 1

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