Found: 18
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Lipophilic aminophosphonates and their calix[4]arene derivatives: synthesis and membrane transport of biorelevant species.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 518, doi. 10.1002/1098-1071(2000)11:7<518::AID-HC10>3.0.CO;2-#
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Erratum: 'On acidification of thiols to produce the corresponding disulfides'.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 583, doi. 10.1002/1098-1071(2000)11:7<583::AID-HC17>3.0.CO;2-N
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Bone active bisphosphonate mechanistic studies: synthesis of a 2-pyrindinylmethylene bisphosphonic acid via a photolytic ring contraction.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 442, doi. 10.1002/1098-1071(2000)11:7<442::AID-HC2>3.0.CO;2-4
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An overview of recent advances on the synthesis and biological activity of α-aminophosphonic acid derivatives.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 480, doi. 10.1002/1098-1071(2000)11:7<480::AID-HC6>3.0.CO;2-J
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A facile asymmetric synthesis of 1-amino-2,2,2-trifluoroethanephosphonic acid.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 536, doi. 10.1002/1098-1071(2000)11:7<536::AID-HC12>3.0.CO;2-Y
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Synthesis of 1-hydroxy-1,1-bisphosphonates.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 556, doi. 10.1002/1098-1071(2000)11:7<556::AID-HC15>3.0.CO;2-N
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What are the requirements in the glyphosate molecule in order for it to be herbicidally active?
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 454, doi. 10.1002/1098-1071(2000)11:7<454::AID-HC4>3.0.CO;2-U
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Syntheses of new racemic N<sup>G</sup>-(1-iminoethyl)phosphalysine derivatives as potential inhibitors of nitric oxide synthase.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 505, doi. 10.1002/1098-1071(2000)11:7<505::AID-HC8>3.0.CO;2-V
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A practical and effective asymmetric synthesis of 2-amino-3,3,3-trifluoropropanephosphonic acid.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 541, doi. 10.1002/1098-1071(2000)11:7<541::AID-HC13>3.0.CO;2-8
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Polycations. IX. Polyammonium derivatives of cyclodextrins: syntheses and binding to organic oxyanions.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 546, doi. 10.1002/1098-1071(2000)11:7<546::AID-HC14>3.0.CO;2-R
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From the editors.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 585, doi. 10.1002/1098-1071(2000)11:7<585::AID-HC18>3.0.CO;2-E
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- Article
Herbicidally active aminomethylenebisphosphonic acids.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 449, doi. 10.1002/1098-1071(2000)11:7<449::AID-HC3>3.0.CO;2-V
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Syntheses, characterization, stereochemistry and complexing properties of acyclic and macrocyclic compounds possessing α-amino- or α-hydroxyphosphonate units: a review article.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 493, doi. 10.1002/1098-1071(2000)11:7<493::AID-HC7>3.0.CO;2-A
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NMR-controlled titrations: characterizing aminophosphonates and related structures.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 562, doi. 10.1002/1098-1071(2000)11:7<562::AID-HC16>3.0.CO;2-V
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From the editors.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 441, doi. 10.1002/1098-1071(2000)11:7<441::AID-HC1>3.0.CO;2-8
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Long-chain functional bisphosphonates: synthesis, anticalcification, and antiresorption activity.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 470, doi. 10.1002/1098-1071(2000)11:7<470::AID-HC5>3.0.CO;2-P
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The reaction of PhCH<sub>2</sub>C(O)NR<sub>2</sub>/P(O)Cl<sub>3</sub> with phosphites and hydridophosphorane.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 512, doi. 10.1002/1098-1071(2000)11:7<512::AID-HC9>3.0.CO;2-S
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A new and efficient asymmetric synthesis of 1-amino-1-alkylphosphonic acids.
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- Heteroatom Chemistry, 2000, v. 11, n. 7, p. 528, doi. 10.1002/1098-1071(2000)11:7<528::AID-HC11>3.0.CO;2-W
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