Kabachnik‐Fields Reaction
Author information unavailable
Abstract
Author information unavailable
Abstract
Abstract A one‐pot synthesis of α‐amino phosphonate via the three‐component coupling of aldehyde (or ketone), an amine, and a dialkylphosphite is generally referred to as the Kabachnik–Fields reaction. It has been reported ketones undergo the coupling more readily than aldehydes, especially for aliphatic ketones that react vigorously. Besides this several other reaction conditions have been discussed to achieve the optimal yields. This reaction has been applied for the preparation of α‐amino phosphonates, which are useful for chelating agents.
OpenAlex reports 3 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract A one‐pot synthesis of α‐amino phosphonate via the three‐component coupling of aldehyde (or ketone), an amine, and a dialkylphosphite is generally referred to as the Kabachnik–Fields reaction. It has been reported ketones undergo the coupling more readily than aldehydes, especially for aliphatic ketones that react vigorously. Besides this several other reaction conditions have been discussed to achieve the optimal yields. This reaction has been applied for the preparation of α‐amino phosphonates, which are useful for chelating agents.
Key concepts: Aldehyde, Phosphonate, Chemistry, Ketone, Amine gas treating, Coupling reaction, Reaction conditions, Chelation