2009
DOI: 10.1134/s1070363209020066
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Synthesis of the first unsymmetrical macroheterocycle containing endocyclic phosphorus atoms from pyrocatechol and hydroquinone

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Cited by 3 publications
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“…Based on bisphosphorylated products generated from aromatic diols, unsymmetrical phosphorus(III)-containing arene macrocycles bearing simultaneously two different diol moieties, such as hydroquinone, di(p-hydroxyphenyl)propane, resorcinol or pyrocatechol, were synthesized by the variative molecular assembly technique. 14,15 For example, compound 10 can be prepared by bisphosphorylation of diol 11 with an excess of phosphorous acid hexaethyltriamide (2b) followed by the reaction of bisphosphorylated product 12 with hydroquinone (13) (Scheme 4). Another sequence of the molecular assembly giving the same product proved to be more efficient.…”
Section: Synthesis Of Phosphorus-containing Crown Ethersmentioning
confidence: 99%
“…Based on bisphosphorylated products generated from aromatic diols, unsymmetrical phosphorus(III)-containing arene macrocycles bearing simultaneously two different diol moieties, such as hydroquinone, di(p-hydroxyphenyl)propane, resorcinol or pyrocatechol, were synthesized by the variative molecular assembly technique. 14,15 For example, compound 10 can be prepared by bisphosphorylation of diol 11 with an excess of phosphorous acid hexaethyltriamide (2b) followed by the reaction of bisphosphorylated product 12 with hydroquinone (13) (Scheme 4). Another sequence of the molecular assembly giving the same product proved to be more efficient.…”
Section: Synthesis Of Phosphorus-containing Crown Ethersmentioning
confidence: 99%