2008
DOI: 10.1002/hc.20502
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Synthesis of Organophosphorus‐Substituted Amides of Carbonic Acids with PCHNC(O) and 2,6‐Di‐tert‐butyl‐4‐methylphenol Fragments

Abstract: Convenient procedures for the synthesis of new organophosphorus-substituted amides of various carbonic acids with PCHNC(O) and 2,6-di-tertbutyl-4-methylphenol (ionol) fragments, starting from the adducts of imines and acyl chlorides, are proposed.Some properties of the new synthesized organophosphorus amides are presented.

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Cited by 17 publications
(2 citation statements)
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“…Hence, adducts A, which are easily formed from anisal(methyl)amine and crotonoyl, cinnamoyl, sorbinoyl, and oleoyl chlorides in methylene chloride (cf. [9]), react with trimethylsilyl phosphites by the Arbuzov reaction scheme to give the corresponding amides 1-5 with high yields (Eq. (1)).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Hence, adducts A, which are easily formed from anisal(methyl)amine and crotonoyl, cinnamoyl, sorbinoyl, and oleoyl chlorides in methylene chloride (cf. [9]), react with trimethylsilyl phosphites by the Arbuzov reaction scheme to give the corresponding amides 1-5 with high yields (Eq. (1)).…”
Section: Resultsmentioning
confidence: 99%
“…In this work, we propose the unique way for the synthesis of new monoand bisorganophosphorus substituted amides of unsaturated carboxylic acids with PCHNC(O) and antioxidant fragments (cf. [9,10]), which was based on available imines and the corresponding acyl chlorides [11], and trimethylsilyl phosphites [12].…”
Section: Introductionmentioning
confidence: 99%