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Article: Synthesis and mass spectrometry of 2-hydroxyethyl 1-aminoalkylphosphonates

TitleSynthesis and mass spectrometry of 2-hydroxyethyl 1-aminoalkylphosphonates
Authors
KeywordsSynthesis
Mannich-type reaction
Multiple component condensation
Aminoalkylphosphonic acid
Amino acid
Mass spectrometry
Alkylphosphonate
Issue Date2007
Citation
Phosphorus, Sulfur and Silicon and the Related Elements, 2007, v. 182, n. 1, p. 25-33 How to Cite?
AbstractMannich-type condensation of benzyl carbamate, aldehydes, and chlorophosphite has been widely used in the synthesis of 1-(N- benzyloxycarbonylamino)arylmethyl-phosphonic derivatives. Reactions of benzyl carbamate, aldehydes, and cyclic chlorophosphite 2-chloro-1,3,2-dioxaphospholane were conducted in benzene to afford a mixture of benzyl [(2-oxido-1,3,2- dioxaphospholane-2-yl)arylmethyl]-carbamates and 2-hydroxyethyl 1-(N-benzoxycarbonylamino)arylmethylphos-phonate monoesters. 2-hydroxyethyl 1-(N-benzoxycarbonylamino)arylmethylphos-phonate monoesters were obtained exclusively after the addition of water under stirring. The reaction mechanism was discussed. Their mass spectrometric fragmentations were also described.
Persistent Identifierhttp://hdl.handle.net/10722/291769
ISSN
2023 Impact Factor: 1.4
2023 SCImago Journal Rankings: 0.240
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorCai, Shuzong-
dc.contributor.authorYin, Wei-
dc.contributor.authorMa, Yuan-
dc.contributor.authorLiu, Han-
dc.contributor.authorZhao, Yufen-
dc.contributor.authorXu, Jiaxi-
dc.date.accessioned2020-11-17T14:55:04Z-
dc.date.available2020-11-17T14:55:04Z-
dc.date.issued2007-
dc.identifier.citationPhosphorus, Sulfur and Silicon and the Related Elements, 2007, v. 182, n. 1, p. 25-33-
dc.identifier.issn1042-6507-
dc.identifier.urihttp://hdl.handle.net/10722/291769-
dc.description.abstractMannich-type condensation of benzyl carbamate, aldehydes, and chlorophosphite has been widely used in the synthesis of 1-(N- benzyloxycarbonylamino)arylmethyl-phosphonic derivatives. Reactions of benzyl carbamate, aldehydes, and cyclic chlorophosphite 2-chloro-1,3,2-dioxaphospholane were conducted in benzene to afford a mixture of benzyl [(2-oxido-1,3,2- dioxaphospholane-2-yl)arylmethyl]-carbamates and 2-hydroxyethyl 1-(N-benzoxycarbonylamino)arylmethylphos-phonate monoesters. 2-hydroxyethyl 1-(N-benzoxycarbonylamino)arylmethylphos-phonate monoesters were obtained exclusively after the addition of water under stirring. The reaction mechanism was discussed. Their mass spectrometric fragmentations were also described.-
dc.languageeng-
dc.relation.ispartofPhosphorus, Sulfur and Silicon and the Related Elements-
dc.subjectSynthesis-
dc.subjectMannich-type reaction-
dc.subjectMultiple component condensation-
dc.subjectAminoalkylphosphonic acid-
dc.subjectAmino acid-
dc.subjectMass spectrometry-
dc.subjectAlkylphosphonate-
dc.titleSynthesis and mass spectrometry of 2-hydroxyethyl 1-aminoalkylphosphonates-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1080/10426500600865251-
dc.identifier.scopuseid_2-s2.0-33845289798-
dc.identifier.volume182-
dc.identifier.issue1-
dc.identifier.spage25-
dc.identifier.epage33-
dc.identifier.eissn1563-5325-
dc.identifier.isiWOS:000242549600004-
dc.identifier.issnl1026-7719-

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