Benign approaches for the synthesis of bis-imine Schiff bases

Tania R. Van Den Ancker; Gareth W.V. Cave; Colin L. Raston

doi:10.1039/b513289d

Benign approaches for the synthesis of bis-imine Schiff bases

Tania R. Van Den Ancker
, Gareth W.V. Cave
, Colin L. Raston

Research output: Contribution to journal › Article › peer-review

46 Citations (Scopus)

Abstract

Pure bis-imine Schiff bases are readily accessible in high yield, typically >95%, when aliphatic diamine/aldehyde condensation reactions are carried out under solvent-free conditions or in poly(propyleneglycol) (PPG) as a recyclable reaction medium, with negligible waste.

Original language	English
Pages (from-to)	50-53
Number of pages	4
Journal	Green Chemistry
Volume	8
Issue number	1
DOIs	https://doi.org/10.1039/b513289d
Publication status	Published - 5 Apr 2006
Externally published	Yes

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title = "Benign approaches for the synthesis of bis-imine Schiff bases",

abstract = "Pure bis-imine Schiff bases are readily accessible in high yield, typically >95\%, when aliphatic diamine/aldehyde condensation reactions are carried out under solvent-free conditions or in poly(propyleneglycol) (PPG) as a recyclable reaction medium, with negligible waste.",

author = "\{Van Den Ancker\}, \{Tania R.\} and Cave, \{Gareth W.V.\} and Raston, \{Colin L.\}",

year = "2006",

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AB - Pure bis-imine Schiff bases are readily accessible in high yield, typically >95%, when aliphatic diamine/aldehyde condensation reactions are carried out under solvent-free conditions or in poly(propyleneglycol) (PPG) as a recyclable reaction medium, with negligible waste.

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U2 - 10.1039/b513289d

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JO - Green Chemistry

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Benign approaches for the synthesis of bis-imine Schiff bases

Abstract

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