Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 27 entries
Sorted by: Best Match Show Resources per page
In-vitro synthesis of marble apatite as a novel adsorbent for removal of fluoride ions from ground water: An ultrasonic approach.

Ultrasonics sonochemistry

Mehta D, Mondal P, Saharan VK, George S.
PMID: 28946471
Ultrason Sonochem. 2018 Jan;40:664-674. doi: 10.1016/j.ultsonch.2017.08.015. Epub 2017 Aug 18.

Marble waste powder consisting of calcium and magnesium compounds was used to synthesize a novel biocompatible product, marble apatite (MA) primarily hydroxyapatite (Hap) for applications in defluoridation of drinking water. Synthesis of marble apatite was carried out by using...

Cite
Mehta D, Mondal P, Saharan VK, et al. In-vitro synthesis of marble apatite as a novel adsorbent for removal of fluoride ions from ground water: An ultrasonic approach. Ultrason Sonochem. 2017;40:664-674doi: 10.1016/j.ultsonch.2017.08.015.
Mehta, D., Mondal, P., Saharan, V. K., & George, S. (2018). In-vitro synthesis of marble apatite as a novel adsorbent for removal of fluoride ions from ground water: An ultrasonic approach. Ultrasonics sonochemistry, 40664-674. https://doi.org/10.1016/j.ultsonch.2017.08.015
Mehta, Dhiraj, et al. "In-vitro synthesis of marble apatite as a novel adsorbent for removal of fluoride ions from ground water: An ultrasonic approach." Ultrasonics sonochemistry vol. 40 (2018): 664-674. doi: https://doi.org/10.1016/j.ultsonch.2017.08.015
Mehta D, Mondal P, Saharan VK, George S. In-vitro synthesis of marble apatite as a novel adsorbent for removal of fluoride ions from ground water: An ultrasonic approach. Ultrason Sonochem. 2018 Jan;40:664-674. doi: 10.1016/j.ultsonch.2017.08.015. Epub 2017 Aug 18. PMID: 28946471.
Copy Download .nbib Format: NLM
Transition-metal-free Sonogashira-type coupling of ortho-substituted aryl and alkynyl Grignard reagents by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical as an oxidant.

Organic letters

Maji MS, Murarka S, Studer A.
PMID: 20704186
Org Lett. 2010 Sep 03;12(17):3878-81. doi: 10.1021/ol1015702.

Cross coupling of aryl, alkenyl, and alkynyl magnesium compounds by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical (TEMPO) as an environmentally benign organic oxidant is described. This coupling reaction can be performed without adding any transition metal on various ortho-substituted aryl and alkynyl...

Cite
Maji MS, Murarka S, Studer A. Transition-metal-free Sonogashira-type coupling of ortho-substituted aryl and alkynyl Grignard reagents by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical as an oxidant. Org Lett. 2010;12(17):3878-81doi: 10.1021/ol1015702.
Maji, M. S., Murarka, S., & Studer, A. (2010). Transition-metal-free Sonogashira-type coupling of ortho-substituted aryl and alkynyl Grignard reagents by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical as an oxidant. Organic letters, 12(17), 3878-81. https://doi.org/10.1021/ol1015702
Maji, Modhu Sudan, et al. "Transition-metal-free Sonogashira-type coupling of ortho-substituted aryl and alkynyl Grignard reagents by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical as an oxidant." Organic letters vol. 12,17 (2010): 3878-81. doi: https://doi.org/10.1021/ol1015702
Maji MS, Murarka S, Studer A. Transition-metal-free Sonogashira-type coupling of ortho-substituted aryl and alkynyl Grignard reagents by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical as an oxidant. Org Lett. 2010 Sep 03;12(17):3878-81. doi: 10.1021/ol1015702. PMID: 20704186.
Copy Download .nbib Format: NLM
Magnesium hydride-promoted dearomatisation of pyridine.

Dalton transactions (Cambridge, England : 2003)

Hill MS, MacDougall DJ, Mahon MF.
PMID: 20959940
Dalton Trans. 2010 Dec 14;39(46):11129-31. doi: 10.1039/c0dt01246g. Epub 2010 Oct 20.

Reaction of pyridine with well defined magnesium hydride species results in heterocycle dearomatisation by a hydride transfer which occurs with the formation of magnesium compounds containing 1,2- and 1,4-dihydropyridide anions as the respective kinetic and thermodynamic products.

Cite
Hill MS, MacDougall DJ, Mahon MF. Magnesium hydride-promoted dearomatisation of pyridine. Dalton Trans. 2010;39(46):11129-31doi: 10.1039/c0dt01246g.
Hill, M. S., MacDougall, D. J., & Mahon, M. F. (2010). Magnesium hydride-promoted dearomatisation of pyridine. Dalton transactions (Cambridge, England : 2003), 39(46), 11129-31. https://doi.org/10.1039/c0dt01246g
Hill, Michael S, et al. "Magnesium hydride-promoted dearomatisation of pyridine." Dalton transactions (Cambridge, England : 2003) vol. 39,46 (2010): 11129-31. doi: https://doi.org/10.1039/c0dt01246g
Hill MS, MacDougall DJ, Mahon MF. Magnesium hydride-promoted dearomatisation of pyridine. Dalton Trans. 2010 Dec 14;39(46):11129-31. doi: 10.1039/c0dt01246g. Epub 2010 Oct 20. PMID: 20959940.
Copy Download .nbib Format: NLM
Volatile magnesium octahydrotriborate complexes as potential CVD precursors to MgB2. Synthesis and characterization of Mg(B3H8)2 and its etherates.

Inorganic chemistry

Kim DY, Yang Y, Abelson JR, Girolami GS.
PMID: 17914810
Inorg Chem. 2007 Oct 29;46(22):9060-6. doi: 10.1021/ic701037t. Epub 2007 Oct 03.

The solid-state reaction of MgBr2 and NaB3H8 at 20 degrees C, followed by sublimation at 80 degrees C and 0.05 Torr, affords Mg(B3H8)2 as a white solid. Similar reactions with MgBr2(Et2O) and MgBr2(Me2O)1.5 afford the crystalline ether adducts Mg(B3H8)2(Et2O)2...

Cite
Kim DY, Yang Y, Abelson JR, et al. Volatile magnesium octahydrotriborate complexes as potential CVD precursors to MgB2. Synthesis and characterization of Mg(B3H8)2 and its etherates. Inorg Chem. 2007;46(22):9060-6doi: 10.1021/ic701037t.
Kim, D. Y., Yang, Y., Abelson, J. R., & Girolami, G. S. (2007). Volatile magnesium octahydrotriborate complexes as potential CVD precursors to MgB2. Synthesis and characterization of Mg(B3H8)2 and its etherates. Inorganic chemistry, 46(22), 9060-6. https://doi.org/10.1021/ic701037t
Kim, Do Young, et al. "Volatile magnesium octahydrotriborate complexes as potential CVD precursors to MgB2. Synthesis and characterization of Mg(B3H8)2 and its etherates." Inorganic chemistry vol. 46,22 (2007): 9060-6. doi: https://doi.org/10.1021/ic701037t
Kim DY, Yang Y, Abelson JR, Girolami GS. Volatile magnesium octahydrotriborate complexes as potential CVD precursors to MgB2. Synthesis and characterization of Mg(B3H8)2 and its etherates. Inorg Chem. 2007 Oct 29;46(22):9060-6. doi: 10.1021/ic701037t. Epub 2007 Oct 03. PMID: 17914810.
Copy Download .nbib Format: NLM
Alkenyl Magnesium Compounds: Generation and Synthetic Application.

Chemistry (Weinheim an der Bergstrasse, Germany)

Zhu M, Liu L, Yu HT, Zhang WX, Xi Z.
PMID: 29984536
Chemistry. 2018 Dec 20;24(72):19122-19135. doi: 10.1002/chem.201802536. Epub 2018 Oct 30.

Alkenyl magnesium compounds have received much attention in synthetic organic chemistry because of their high reactivity. This review summarizes three types of alkenyl magnesium compounds which contain at least one [Mg-C=C] fragment, for example, (1) alkenyl Grignard reagents prepared...

Cite
Zhu M, Liu L, Yu HT, et al. Alkenyl Magnesium Compounds: Generation and Synthetic Application. Chemistry. 2018;24(72):19122-19135doi: 10.1002/chem.201802536.
Zhu, M., Liu, L., Yu, H. T., Zhang, W. X., & Xi, Z. (2018). Alkenyl Magnesium Compounds: Generation and Synthetic Application. Chemistry (Weinheim an der Bergstrasse, Germany), 24(72), 19122-19135. https://doi.org/10.1002/chem.201802536
Zhu, Miaomiao, et al. "Alkenyl Magnesium Compounds: Generation and Synthetic Application." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 24,72 (2018): 19122-19135. doi: https://doi.org/10.1002/chem.201802536
Zhu M, Liu L, Yu HT, Zhang WX, Xi Z. Alkenyl Magnesium Compounds: Generation and Synthetic Application. Chemistry. 2018 Dec 20;24(72):19122-19135. doi: 10.1002/chem.201802536. Epub 2018 Oct 30. PMID: 29984536.
Copy Download .nbib Format: NLM
Synthesis, Characterization, and Cellular Uptake of Magnesium Maltol and Ethylmaltol Complexes.

ACS omega

Case DR, Gonzalez R, Zubieta J, Doyle RP.
PMID: 34778643
ACS Omega. 2021 Oct 28;6(44):29713-29723. doi: 10.1021/acsomega.1c04104. eCollection 2021 Nov 09.

Magnesium deficiency and/or deficit (hypomagnesemia,

Cite
Case DR, Gonzalez R, Zubieta J, et al. Synthesis, Characterization, and Cellular Uptake of Magnesium Maltol and Ethylmaltol Complexes. ACS Omega. 2021;6(44):29713-29723doi: 10.1021/acsomega.1c04104.
Case, D. R., Gonzalez, R., Zubieta, J., & Doyle, R. P. (2021). Synthesis, Characterization, and Cellular Uptake of Magnesium Maltol and Ethylmaltol Complexes. ACS omega, 6(44), 29713-29723. https://doi.org/10.1021/acsomega.1c04104
Case, Derek R, et al. "Synthesis, Characterization, and Cellular Uptake of Magnesium Maltol and Ethylmaltol Complexes." ACS omega vol. 6,44 (2021): 29713-29723. doi: https://doi.org/10.1021/acsomega.1c04104
Case DR, Gonzalez R, Zubieta J, Doyle RP. Synthesis, Characterization, and Cellular Uptake of Magnesium Maltol and Ethylmaltol Complexes. ACS Omega. 2021 Oct 28;6(44):29713-29723. doi: 10.1021/acsomega.1c04104. eCollection 2021 Nov 09. PMID: 34778643; PMCID: PMC8587132.
Copy Download .nbib Format: NLM
Divinyl-end-functionalized polyethylenes: ready access to a range of telechelic polyethylenes through thiol-ene reactions.

Angewandte Chemie (International ed. in English)

Norsic S, Thomas C, D'Agosto F, Boisson C.
PMID: 25688747
Angew Chem Int Ed Engl. 2015 Apr 07;54(15):4631-5. doi: 10.1002/anie.201411223. Epub 2015 Feb 16.

Telechelic α,ω-iodo-vinyl-polyethylenes (Vin-PE-I) were obtained by catalytic ethylene polymerization in the presence of [(C5 Me5 )2 NdCl2 Li(OEt2 )2 ] in combination with a functionalized chain-transfer agent, namely, di(10-undecenyl)magnesium, followed by treatment of the resulting di(vinylpolyethylenyl)magnesium compounds ((vinyl-PE)2 Mg)...

Cite
Norsic S, Thomas C, D'Agosto F, et al. Divinyl-end-functionalized polyethylenes: ready access to a range of telechelic polyethylenes through thiol-ene reactions. Angew Chem Int Ed Engl. 2015;54(15):4631-5doi: 10.1002/anie.201411223.
Norsic, S., Thomas, C., D'Agosto, F., & Boisson, C. (2015). Divinyl-end-functionalized polyethylenes: ready access to a range of telechelic polyethylenes through thiol-ene reactions. Angewandte Chemie (International ed. in English), 54(15), 4631-5. https://doi.org/10.1002/anie.201411223
Norsic, Sebastien, et al. "Divinyl-end-functionalized polyethylenes: ready access to a range of telechelic polyethylenes through thiol-ene reactions." Angewandte Chemie (International ed. in English) vol. 54,15 (2015): 4631-5. doi: https://doi.org/10.1002/anie.201411223
Norsic S, Thomas C, D'Agosto F, Boisson C. Divinyl-end-functionalized polyethylenes: ready access to a range of telechelic polyethylenes through thiol-ene reactions. Angew Chem Int Ed Engl. 2015 Apr 07;54(15):4631-5. doi: 10.1002/anie.201411223. Epub 2015 Feb 16. PMID: 25688747.
Copy Download .nbib Format: NLM
An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate.

The Journal of organic chemistry

Bhagat S, Chakraborti AK.
PMID: 17253748
J Org Chem. 2007 Feb 16;72(4):1263-70. doi: 10.1021/jo062140i. Epub 2007 Jan 25.

Commercially available magnesium perchlorate is reported as an extremely efficient catalyst for the synthesis of alpha-aminophosphonates. A three-component reaction (3-CR) of an amine, an aldehyde or a ketone, and a di-/trialkyl phosphite (Kabachnik-Fields reaction) took place in one pot...

Cite
Bhagat S, Chakraborti AK. An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate. J Org Chem. 2007;72(4):1263-70doi: 10.1021/jo062140i.
Bhagat, S., & Chakraborti, A. K. (2007). An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate. The Journal of organic chemistry, 72(4), 1263-70. https://doi.org/10.1021/jo062140i
Bhagat, Srikant, and Chakraborti, Asit K. "An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate." The Journal of organic chemistry vol. 72,4 (2007): 1263-70. doi: https://doi.org/10.1021/jo062140i
Bhagat S, Chakraborti AK. An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate. J Org Chem. 2007 Feb 16;72(4):1263-70. doi: 10.1021/jo062140i. Epub 2007 Jan 25. PMID: 17253748.
Copy Download .nbib Format: NLM
Facile high-yield synthesis of pure, crystalline Mg(BH4)2.

Inorganic chemistry

Zanella P, Crociani L, Masciocchi N, Giunchi G.
PMID: 17900187
Inorg Chem. 2007 Oct 29;46(22):9039-41. doi: 10.1021/ic701436c. Epub 2007 Sep 28.

Magnesium borohydride, Mg(BH4)2, a long-sought candidate for efficient hydrogen storage chemisorption technology, has been obtained in a pure and crystalline form by two new synthetic routes in a hydrocarbon solvent. A first synthetic approach involves a metathetical reaction between...

Cite
Zanella P, Crociani L, Masciocchi N, et al. Facile high-yield synthesis of pure, crystalline Mg(BH4)2. Inorg Chem. 2007;46(22):9039-41doi: 10.1021/ic701436c.
Zanella, P., Crociani, L., Masciocchi, N., & Giunchi, G. (2007). Facile high-yield synthesis of pure, crystalline Mg(BH4)2. Inorganic chemistry, 46(22), 9039-41. https://doi.org/10.1021/ic701436c
Zanella, Pierino, et al. "Facile high-yield synthesis of pure, crystalline Mg(BH4)2." Inorganic chemistry vol. 46,22 (2007): 9039-41. doi: https://doi.org/10.1021/ic701436c
Zanella P, Crociani L, Masciocchi N, Giunchi G. Facile high-yield synthesis of pure, crystalline Mg(BH4)2. Inorg Chem. 2007 Oct 29;46(22):9039-41. doi: 10.1021/ic701436c. Epub 2007 Sep 28. PMID: 17900187.
Copy Download .nbib Format: NLM
Availability of magnesium from various commercially available oral preparations in a variety of dosage forms: comparative in vitro study.

Journal of medicinal food

Steinmetz T, Fortmann-Mölling B, Wenisch S, Leonhäuser IU.
PMID: 19281350
J Med Food. 1999;2(2):65-71. doi: 10.1089/jmf.1999.2.65.

The relative dialysability of magnesium in a number of different inorganic and organic magnesium-containing compounds from ten commercially available products was investigated using an in vitro method. Reference values were provided by tests carried out in parallel using comparable...

Cite
Steinmetz T, Fortmann-Mölling B, Wenisch S, et al. Availability of magnesium from various commercially available oral preparations in a variety of dosage forms: comparative in vitro study. J Med Food. 1999;2(2):65-71doi: 10.1089/jmf.1999.2.65.
Steinmetz, T., Fortmann-Mölling, B., Wenisch, S., & Leonhäuser, I. U. (1999). Availability of magnesium from various commercially available oral preparations in a variety of dosage forms: comparative in vitro study. Journal of medicinal food, 2(2), 65-71. https://doi.org/10.1089/jmf.1999.2.65
Steinmetz, T, et al. "Availability of magnesium from various commercially available oral preparations in a variety of dosage forms: comparative in vitro study." Journal of medicinal food vol. 2,2 (1999): 65-71. doi: https://doi.org/10.1089/jmf.1999.2.65
Steinmetz T, Fortmann-Mölling B, Wenisch S, Leonhäuser IU. Availability of magnesium from various commercially available oral preparations in a variety of dosage forms: comparative in vitro study. J Med Food. 1999;2(2):65-71. doi: 10.1089/jmf.1999.2.65. PMID: 19281350.
Copy Download .nbib Format: NLM
Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium.

ACS omega

Case DR, Gonzalez R, Zubieta J, Doyle RP.
PMID: 34926895
ACS Omega. 2021 Nov 30;6(49):33454-33461. doi: 10.1021/acsomega.1c04146. eCollection 2021 Dec 14.

Human chronic latent magnesium deficiency is estimated to impact a substantive portion of the world's population. A number of magnesium compounds have been developed to combat this deficiency; however, none are ideal due to issues of solubility, absorption, side...

Cite
Case DR, Gonzalez R, Zubieta J, et al. Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium. ACS Omega. 2021;6(49):33454-33461doi: 10.1021/acsomega.1c04146.
Case, D. R., Gonzalez, R., Zubieta, J., & Doyle, R. P. (2021). Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium. ACS omega, 6(49), 33454-33461. https://doi.org/10.1021/acsomega.1c04146
Case, Derek R, et al. "Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium." ACS omega vol. 6,49 (2021): 33454-33461. doi: https://doi.org/10.1021/acsomega.1c04146
Case DR, Gonzalez R, Zubieta J, Doyle RP. Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium. ACS Omega. 2021 Nov 30;6(49):33454-33461. doi: 10.1021/acsomega.1c04146. eCollection 2021 Dec 14. PMID: 34926895; PMCID: PMC8679001.
Copy Download .nbib Format: NLM
Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium.

ACS omega

Case DR, Gonzalez R, Zubieta J, Doyle RP.
PMID: 34926895
ACS Omega. 2021 Nov 30;6(49):33454-33461. doi: 10.1021/acsomega.1c04146. eCollection 2021 Dec 14.

Human chronic latent magnesium deficiency is estimated to impact a substantive portion of the world's population. A number of magnesium compounds have been developed to combat this deficiency; however, none are ideal due to issues of solubility, absorption, side...

Cite
Case DR, Gonzalez R, Zubieta J, et al. Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium. ACS Omega. 2021;6(49):33454-33461doi: 10.1021/acsomega.1c04146.
Case, D. R., Gonzalez, R., Zubieta, J., & Doyle, R. P. (2021). Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium. ACS omega, 6(49), 33454-33461. https://doi.org/10.1021/acsomega.1c04146
Case, Derek R, et al. "Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium." ACS omega vol. 6,49 (2021): 33454-33461. doi: https://doi.org/10.1021/acsomega.1c04146
Case DR, Gonzalez R, Zubieta J, Doyle RP. Synthesis, Characterization, and Cellular Uptake of a Glycylglycine Chelate of Magnesium. ACS Omega. 2021 Nov 30;6(49):33454-33461. doi: 10.1021/acsomega.1c04146. eCollection 2021 Dec 14. PMID: 34926895; PMCID: PMC8679001.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 27 entries