Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/154630
Title: Air-stable phosphine organocatalysts for the hydroarsination reaction
Authors: Tay, Wee Shan
Li, Yongxin
Yang, Xiang-Yuan
Pullarkat, Sumod Appukuttan
Leung, Pak-Hing
Keywords: Science::Chemistry
Issue Date: 2020
Source: Tay, W. S., Li, Y., Yang, X., Pullarkat, S. A. & Leung, P. (2020). Air-stable phosphine organocatalysts for the hydroarsination reaction. Journal of Organometallic Chemistry, 914, 121216-. https://dx.doi.org/10.1016/j.jorganchem.2020.121216
Project: M401110000 RG 10/19
Journal: Journal of Organometallic Chemistry
Abstract: Readily-available triarylphosphines are explored as organocatalysts for the hydroarsination reaction. When compared to transition metal catalysis, phosphine organocatalysis greatly improved solvent compatibility of the hydroarsination of nitrostyrenes. Upon complete conversion, arsine products were isolated in up to 99% yield while up to 48% of the phosphine catalyst was still active. A mechanism was proposed and structure-activity analysis regarding catalyst activity concluded that sterically-bulkier catalysts were effective at minimizing catalyst deactivation.
URI: https://hdl.handle.net/10356/154630
ISSN: 0022-328X
DOI: 10.1016/j.jorganchem.2020.121216
Rights: © 2020 Published by Elsevier B.V. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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