Repurposing cycloaddition of β-carbonyl phosphonate and azide to synthesize triazolyl phosphonates <i>via</i> ionic-liquid-based data-driven screening-Reference-Cited by-同舟云学术

Repurposing cycloaddition of β-carbonyl phosphonate and azide to synthesize triazolyl phosphonates via ionic-liquid-based data-driven screening

Published:2022 Issue:21 Volume:24 Page:8466-8476
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zhu Anlian¹,Fan Dongshuang¹,You Yanbo¹,Wang Honglei¹²,Zhao Yang¹,Wang Jianji¹^ORCID,Li Lingjun¹²^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Henan Key Laboratory of Organic Functional Molecule and Drug Innovation, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Normal University, Xinxiang, Henan 453007, China

2. State Key Laboratory of Cell Differentiation Regulation and Target Drug, Henan Normal University, Xinxiang 453007, China

Abstract

Triazolyl phosphonates can be synthesized in the all-in-one ionic liquid reaction system, which are discovered by data-driven screening.

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/2022/GC/D2GC02461F

Reference60 articles.

1. Isolation of 2-Aminoethane Phosphonic Acid from Rumen Protozoa

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