Disulfide Promoted C−P Bond Cleavage of Phosphoramide: “P” Surrogates to Synthesize Phosphonates and Phosphinates-Reference-Cited by-同舟云学术

Disulfide Promoted C−P Bond Cleavage of Phosphoramide: “P” Surrogates to Synthesize Phosphonates and Phosphinates

Published:2020-10 Issue:21 Volume:362 Page:4755-4760
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Hou Fei¹,Du Xing‐Peng¹,Alduma Anwar I.¹,Li Zhi‐Feng²,Huo Cong‐De¹,Wang Xi‐Cun¹,Wu Xiao‐Feng¹³,Quan Zheng‐Jun¹

Affiliation:

1. International Scientific and Technological Cooperation Base of Water Retention Chemical Functional Materials College of Chemistry and Chemical Engineering Northwest Normal University Lanzhou Gansu 730070 People's Republic of China

2. College of Chemical Engineering and Technology Key Laboratory for New Molecule Design and Function of Gansu Universities Tianshui Normal University Tianshui 741001 People's Republic of China

3. Department of Chemistry University of Liverpool Crown Street Liverpool L69 7ZD UK

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202000511

Reference122 articles.

2. Surface Modification Using Phosphonic Acids and Esters

3. Enantioselective Esterification of Prochiral Phosphonate Pendants of a Polyphenylacetylene Assisted by Macromolecular Helicity: Storage of a Dynamic Macromolecular Helicity Memory

5. Review on Modern Advances of Chemical Methods for the Introduction of a Phosphonic Acid Group

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