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Synthesis of new functionalized mono‐ and bisphosphinates with 2,6‐di‐tert‐butyl‐4‐methylphenol fragments

Synthesis of new functionalized mono‐ and bisphosphinates with 2,6‐di‐tert‐butyl‐4‐methylphenol... Convenient procedures for the synthesis of functionalized mono‐ and bisphosphinates with 2,6‐di‐tert‐butyl‐4‐methylphenol (ionol) fragments, starting from the available 3,5‐di‐tert‐butyl‐4‐benzaldehyde and its derivatives, are proposed, and some properties of the new phosphorus‐substituted sterically hindered phenols are presented. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:562–568, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20475 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

Synthesis of new functionalized mono‐ and bisphosphinates with 2,6‐di‐tert‐butyl‐4‐methylphenol fragments

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References (6)

Publisher
Wiley
Copyright
Copyright © 2008 Wiley Periodicals, Inc.
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/hc.20475
Publisher site
See Article on Publisher Site

Abstract

Convenient procedures for the synthesis of functionalized mono‐ and bisphosphinates with 2,6‐di‐tert‐butyl‐4‐methylphenol (ionol) fragments, starting from the available 3,5‐di‐tert‐butyl‐4‐benzaldehyde and its derivatives, are proposed, and some properties of the new phosphorus‐substituted sterically hindered phenols are presented. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:562–568, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20475

Journal

Heteroatom ChemistryWiley

Published: Sep 1, 2008

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