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DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions.

Synlett : accounts and rapid communications in synthetic organic chemistry

Reilly MK, Rychnovsky SD.
PMID: 24371372
Synlett. 2011 Oct 01;2011(16). doi: 10.1055/s-0030-1261218.

Diethanolamine complexed heterocyclic boronic acids (DABO boronates) are air-stable reagents that can be used directly in Suzuki-Miyaura reactions in the presence of water or a protic co-solvent. Interestingly, heterocyclic DABO boronates can be stored for extended periods of time...

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Reilly MK, Rychnovsky SD. DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions. Synlett. 2011;2011(16)doi: 10.1055/s-0030-1261218.
Reilly, M. K., & Rychnovsky, S. D. (2011). DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions. Synlett : accounts and rapid communications in synthetic organic chemistry, 2011(16), . https://doi.org/10.1055/s-0030-1261218
Reilly, Maureen K, and Rychnovsky, Scott D. "DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions." Synlett : accounts and rapid communications in synthetic organic chemistry vol. 2011,16 (2011). doi: https://doi.org/10.1055/s-0030-1261218
Reilly MK, Rychnovsky SD. DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions. Synlett. 2011 Oct 01;2011(16). doi: 10.1055/s-0030-1261218. PMID: 24371372; PMCID: PMC3870905.
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Laboratory and clinical trials of cocamide diethanolamine lotion against head lice.

PeerJ

Burgess IF, Brunton ER, Brown CM.
PMID: 26557439
PeerJ. 2015 Nov 03;3:e1368. doi: 10.7717/peerj.1368. eCollection 2015.

Context. During the late 1990s, insecticide resistance had rendered a number of treatment products ineffective; some companies saw this as an opportunity to develop alternative types of treatment. We investigated the possibility that a surfactant-based lotion containing 10% cocamide...

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Burgess IF, Brunton ER, Brown CM. Laboratory and clinical trials of cocamide diethanolamine lotion against head lice. PeerJ. 2015;3:e1368doi: 10.7717/peerj.1368.
Burgess, I. F., Brunton, E. R., & Brown, C. M. (2015). Laboratory and clinical trials of cocamide diethanolamine lotion against head lice. PeerJ, 3e1368. https://doi.org/10.7717/peerj.1368
Burgess, Ian F, et al. "Laboratory and clinical trials of cocamide diethanolamine lotion against head lice." PeerJ vol. 3 (2015): e1368. doi: https://doi.org/10.7717/peerj.1368
Burgess IF, Brunton ER, Brown CM. Laboratory and clinical trials of cocamide diethanolamine lotion against head lice. PeerJ. 2015 Nov 03;3:e1368. doi: 10.7717/peerj.1368. eCollection 2015. PMID: 26557439; PMCID: PMC4636399.
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Diclofenac Salts, VIII. Effect of the Counterions on the Permeation through Porcine Membrane from Aqueous Saturated Solutions.

Pharmaceutics

Fini A, Bassini G, Monastero A, Cavallari C.
PMID: 24300300
Pharmaceutics. 2012 Sep 12;4(3):413-29. doi: 10.3390/pharmaceutics4030413.

The following bases: monoethylamine (EtA), diethylamine (DEtA), triethylamine (TEtA), monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), pyrrolidine (Py), piperidine (Pp), morpholine (M), piperazine (Pz) and their N-2-hydroxyethyl (HE) analogs were employed to prepare 14 diclofenac salts. The salts were re-crystallized...

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Fini A, Bassini G, Monastero A, et al. Diclofenac Salts, VIII. Effect of the Counterions on the Permeation through Porcine Membrane from Aqueous Saturated Solutions. Pharmaceutics. 2012;4(3):413-29doi: 10.3390/pharmaceutics4030413.
Fini, A., Bassini, G., Monastero, A., & Cavallari, C. (2012). Diclofenac Salts, VIII. Effect of the Counterions on the Permeation through Porcine Membrane from Aqueous Saturated Solutions. Pharmaceutics, 4(3), 413-29. https://doi.org/10.3390/pharmaceutics4030413
Fini, Adamo, et al. "Diclofenac Salts, VIII. Effect of the Counterions on the Permeation through Porcine Membrane from Aqueous Saturated Solutions." Pharmaceutics vol. 4,3 (2012): 413-29. doi: https://doi.org/10.3390/pharmaceutics4030413
Fini A, Bassini G, Monastero A, Cavallari C. Diclofenac Salts, VIII. Effect of the Counterions on the Permeation through Porcine Membrane from Aqueous Saturated Solutions. Pharmaceutics. 2012 Sep 12;4(3):413-29. doi: 10.3390/pharmaceutics4030413. PMID: 24300300; PMCID: PMC3834916.
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Acyclic N-halamine-immobilized polyurethane: Preparation and antimicrobial and biofilm-controlling functions.

Journal of bioactive and compatible polymers

Luo J, Porteous N, Lin J, Sun Y.
PMID: 26089593
J Bioact Compat Polym. 2015 Mar;30(2):157-166. doi: 10.1177/0883911515569007.

Hydroxyl groups were introduced onto polyurethane surfaces through 1,6-hexamethylene diisocyanate activation, followed by diethanolamine hydroxylation. Polymethacrylamide was covalently attached to the hydroxylated polyurethane through surface grafting polymerization of methacrylamide using cerium (IV) ammonium nitrate as an initiator. After bleach...

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Luo J, Porteous N, Lin J, et al. Acyclic N-halamine-immobilized polyurethane: Preparation and antimicrobial and biofilm-controlling functions. J Bioact Compat Polym. 2015;30(2):157-166doi: 10.1177/0883911515569007.
Luo, J., Porteous, N., Lin, J., & Sun, Y. (2015). Acyclic N-halamine-immobilized polyurethane: Preparation and antimicrobial and biofilm-controlling functions. Journal of bioactive and compatible polymers, 30(2), 157-166. https://doi.org/10.1177/0883911515569007
Luo, Jie, et al. "Acyclic N-halamine-immobilized polyurethane: Preparation and antimicrobial and biofilm-controlling functions." Journal of bioactive and compatible polymers vol. 30,2 (2015): 157-166. doi: https://doi.org/10.1177/0883911515569007
Luo J, Porteous N, Lin J, Sun Y. Acyclic N-halamine-immobilized polyurethane: Preparation and antimicrobial and biofilm-controlling functions. J Bioact Compat Polym. 2015 Mar;30(2):157-166. doi: 10.1177/0883911515569007. PMID: 26089593; PMCID: PMC4469204.
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Solutions of complex copper salts in low-transition-temperature mixture (LTTM).

Dalton transactions (Cambridge, England : 2003)

Zakharov MA, Fetisov GV, Veligzhanin AA, Bykov MA, Paseshnichenko KA, Dunaev SF, Aslanov LA.
PMID: 26448612
Dalton Trans. 2015 Nov 14;44(42):18576-84. doi: 10.1039/c5dt02941d. Epub 2015 Oct 08.

The structure and properties of diethanolamine complexes of copper(ii) triflates dissolved in an excess of diethanolamine (DH2) were studied. The copper containing substance was found to be a solution of copper(ii) complex salt [Cu(2+)DH2(DH(-))]OTf(-) in LTTM composition [(DH2)4H(+)](OTf(-)), where...

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Zakharov MA, Fetisov GV, Veligzhanin AA, et al. Solutions of complex copper salts in low-transition-temperature mixture (LTTM). Dalton Trans. 2015;44(42):18576-84doi: 10.1039/c5dt02941d.
Zakharov, M. A., Fetisov, G. V., Veligzhanin, A. A., Bykov, M. A., Paseshnichenko, K. A., Dunaev, S. F., & Aslanov, L. A. (2015). Solutions of complex copper salts in low-transition-temperature mixture (LTTM). Dalton transactions (Cambridge, England : 2003), 44(42), 18576-84. https://doi.org/10.1039/c5dt02941d
Zakharov, Maxim A, et al. "Solutions of complex copper salts in low-transition-temperature mixture (LTTM)." Dalton transactions (Cambridge, England : 2003) vol. 44,42 (2015): 18576-84. doi: https://doi.org/10.1039/c5dt02941d
Zakharov MA, Fetisov GV, Veligzhanin AA, Bykov MA, Paseshnichenko KA, Dunaev SF, Aslanov LA. Solutions of complex copper salts in low-transition-temperature mixture (LTTM). Dalton Trans. 2015 Nov 14;44(42):18576-84. doi: 10.1039/c5dt02941d. Epub 2015 Oct 08. PMID: 26448612.
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Decarboxylation and simultaneous reduction of silver(I) β-ketocarboxylates with three types of coordinations.

Dalton transactions (Cambridge, England : 2003)

Hatamura M, Yamaguchi S, Takane SY, Chen Y, Suganuma K.
PMID: 25882627
Dalton Trans. 2015 May 21;44(19):8993-9003. doi: 10.1039/c5dt00773a.

A series of silver(I) β-ketocarboxylates were prepared by reaction of β-ketocarboxylic acids with silver nitrate in the presence of diethanolamine. The silver(I) β-ketocarboxylates decomposed over a narrow temperature range to form metallic silver, CO2, and the corresponding ketones. In...

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Hatamura M, Yamaguchi S, Takane SY, et al. Decarboxylation and simultaneous reduction of silver(I) β-ketocarboxylates with three types of coordinations. Dalton Trans. 2015;44(19):8993-9003doi: 10.1039/c5dt00773a.
Hatamura, M., Yamaguchi, S., Takane, S. Y., Chen, Y., & Suganuma, K. (2015). Decarboxylation and simultaneous reduction of silver(I) β-ketocarboxylates with three types of coordinations. Dalton transactions (Cambridge, England : 2003), 44(19), 8993-9003. https://doi.org/10.1039/c5dt00773a
Hatamura, Mariko, et al. "Decarboxylation and simultaneous reduction of silver(I) β-ketocarboxylates with three types of coordinations." Dalton transactions (Cambridge, England : 2003) vol. 44,19 (2015): 8993-9003. doi: https://doi.org/10.1039/c5dt00773a
Hatamura M, Yamaguchi S, Takane SY, Chen Y, Suganuma K. Decarboxylation and simultaneous reduction of silver(I) β-ketocarboxylates with three types of coordinations. Dalton Trans. 2015 May 21;44(19):8993-9003. doi: 10.1039/c5dt00773a. PMID: 25882627.
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trans-Bis(diethanolamine-N,O)bis(saccharinato-N)cadmium(II).

Acta crystallographica. Section C, Crystal structure communications

Andac O, Topcu Y, Yilmaz VT, Harrison WT.
PMID: 11781458
Acta Crystallogr C. 2002 Jan;58:m14-6. doi: 10.1107/s0108270101018546. Epub 2001 Dec 14.

The structure of the title complex consists of isolated [Cd(C7H4NO3S)2(C4H11NO2)2] units. The Cd2+ cation lies on an inversion centre and is octahedrally coordinated by two N,O-bidentate diethanolamine (dea) and two N-bonded saccharinate (sac) ligands [saccharin is 1,2-benzisothiazol-3(2H)-one 1,1-dioxide]. The...

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Andac O, Topcu Y, Yilmaz VT, et al. trans-Bis(diethanolamine-N,O)bis(saccharinato-N)cadmium(II). Acta Crystallogr C. 2001;58:m14-6doi: 10.1107/s0108270101018546.
Andac, O., Topcu, Y., Yilmaz, V. T., & Harrison, W. T. (2002). trans-Bis(diethanolamine-N,O)bis(saccharinato-N)cadmium(II). Acta crystallographica. Section C, Crystal structure communications, 58m14-6. https://doi.org/10.1107/s0108270101018546
Andac, Omer, et al. "trans-Bis(diethanolamine-N,O)bis(saccharinato-N)cadmium(II)." Acta crystallographica. Section C, Crystal structure communications vol. 58 (2002): m14-6. doi: https://doi.org/10.1107/s0108270101018546
Andac O, Topcu Y, Yilmaz VT, Harrison WT. trans-Bis(diethanolamine-N,O)bis(saccharinato-N)cadmium(II). Acta Crystallogr C. 2002 Jan;58:m14-6. doi: 10.1107/s0108270101018546. Epub 2001 Dec 14. PMID: 11781458.
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Synthesis, structure, and dynamics of six-membered metallacoronands and metallodendrimers of iron and indium.

Chemistry (Weinheim an der Bergstrasse, Germany)

Saalfrank RW, Deutscher C, Maid H, Ako AM, Sperner S, Nakajima T, Bauer W, Hampel F, Hess BA, van Eikema Hommes NJ, Puchta R, Heinemann FW.
PMID: 15079828
Chemistry. 2004 Apr 19;10(8):1899-905. doi: 10.1002/chem.200306050.

In the reaction of the N-substituted diethanolamines (H(2)L(1-3)) (1-3) with calcium hydride followed by addition of iron(III) or indium(III) chloride, the iron wheels [Fe(6)Cl(6)(L(1))(6)] (4) and [Fe(6)Cl(6)(L(2))(6)] (6) or indium wheels [In(6)Cl(6)(L(1))(6)] (5), [In(6)Cl(6)(L(2))(6)] (8) and [In(6)Cl(6)(L(3))(6)] (9) were...

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Saalfrank RW, Deutscher C, Maid H, et al. Synthesis, structure, and dynamics of six-membered metallacoronands and metallodendrimers of iron and indium. Chemistry. 2004;10(8):1899-905doi: 10.1002/chem.200306050.
Saalfrank, R. W., Deutscher, C., Maid, H., Ako, A. M., Sperner, S., Nakajima, T., Bauer, W., Hampel, F., Hess, B. A., van Eikema Hommes, N. J., Puchta, R., & Heinemann, F. W. (2004). Synthesis, structure, and dynamics of six-membered metallacoronands and metallodendrimers of iron and indium. Chemistry (Weinheim an der Bergstrasse, Germany), 10(8), 1899-905. https://doi.org/10.1002/chem.200306050
Saalfrank, Rolf W, et al. "Synthesis, structure, and dynamics of six-membered metallacoronands and metallodendrimers of iron and indium." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 10,8 (2004): 1899-905. doi: https://doi.org/10.1002/chem.200306050
Saalfrank RW, Deutscher C, Maid H, Ako AM, Sperner S, Nakajima T, Bauer W, Hampel F, Hess BA, van Eikema Hommes NJ, Puchta R, Heinemann FW. Synthesis, structure, and dynamics of six-membered metallacoronands and metallodendrimers of iron and indium. Chemistry. 2004 Apr 19;10(8):1899-905. doi: 10.1002/chem.200306050. PMID: 15079828.
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Assembling novel heterotrimetallic Cu/Co/Ni and Cu/Co/Cd cores supported by diethanolamine ligand in one-pot reactions of zerovalent copper with metal salts.

Inorganic chemistry

Nesterov DS, Makhankova VG, Vassilyeva OY, Kokozay VN, Kovbasyuk LA, Skelton BW, Jezierska J.
PMID: 15554652
Inorg Chem. 2004 Nov 29;43(24):7868-76. doi: 10.1021/ic048955w.

The three novel heterotrimetallic complexes [Ni(H2L)2][CoCu(L)2(H2L)(NCS)]2(NCS)2 (1), [Ni(H2L)2][CuCo(L)2(H2L)(NCS)]2Br2.2H2O (2), and [CuCoCd(H2L)2(L)2(NCS)Br2].CH3OH (3) have been prepared using zerovalent copper; cobalt thiocyanate; nickel thiocyanate (1), nickel bromide (2), or cadmium bromide (3); and methanol solutions of diethanolamine in air. The most...

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Nesterov DS, Makhankova VG, Vassilyeva OY, et al. Assembling novel heterotrimetallic Cu/Co/Ni and Cu/Co/Cd cores supported by diethanolamine ligand in one-pot reactions of zerovalent copper with metal salts. Inorg Chem. 2004;43(24):7868-76doi: 10.1021/ic048955w.
Nesterov, D. S., Makhankova, V. G., Vassilyeva, O. Y., Kokozay, V. N., Kovbasyuk, L. A., Skelton, B. W., & Jezierska, J. (2004). Assembling novel heterotrimetallic Cu/Co/Ni and Cu/Co/Cd cores supported by diethanolamine ligand in one-pot reactions of zerovalent copper with metal salts. Inorganic chemistry, 43(24), 7868-76. https://doi.org/10.1021/ic048955w
Nesterov, Dmytro S, et al. "Assembling novel heterotrimetallic Cu/Co/Ni and Cu/Co/Cd cores supported by diethanolamine ligand in one-pot reactions of zerovalent copper with metal salts." Inorganic chemistry vol. 43,24 (2004): 7868-76. doi: https://doi.org/10.1021/ic048955w
Nesterov DS, Makhankova VG, Vassilyeva OY, Kokozay VN, Kovbasyuk LA, Skelton BW, Jezierska J. Assembling novel heterotrimetallic Cu/Co/Ni and Cu/Co/Cd cores supported by diethanolamine ligand in one-pot reactions of zerovalent copper with metal salts. Inorg Chem. 2004 Nov 29;43(24):7868-76. doi: 10.1021/ic048955w. PMID: 15554652.
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Determination of water samples and ene-diols or thiols in samples inaccessible for direct K.Fischer titration.

Talanta

Sherman F, Kuselman I, Shenhar A.
PMID: 18966577
Talanta. 1996 Jul;43(7):1035-42. doi: 10.1016/0039-9140(96)01852-8.

Novel reagents and the rapid technique were developed for the simultaneous determination of water and ene-diols or thiols in chemical products, drugs and other materials which are inaccessible for direct K.Fischer titration. The reagents consist of iodine, tetramethylammonium iodide...

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Sherman F, Kuselman I, Shenhar A. Determination of water samples and ene-diols or thiols in samples inaccessible for direct K.Fischer titration. Talanta. 1996;43(7):1035-42doi: 10.1016/0039-9140(96)01852-8.
Sherman, F., Kuselman, I., & Shenhar, A. (1996). Determination of water samples and ene-diols or thiols in samples inaccessible for direct K.Fischer titration. Talanta, 43(7), 1035-42. https://doi.org/10.1016/0039-9140(96)01852-8
Sherman, F, et al. "Determination of water samples and ene-diols or thiols in samples inaccessible for direct K.Fischer titration." Talanta vol. 43,7 (1996): 1035-42. doi: https://doi.org/10.1016/0039-9140(96)01852-8
Sherman F, Kuselman I, Shenhar A. Determination of water samples and ene-diols or thiols in samples inaccessible for direct K.Fischer titration. Talanta. 1996 Jul;43(7):1035-42. doi: 10.1016/0039-9140(96)01852-8. PMID: 18966577.
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Reduction of nitrosamines in cosmetic products.

International journal of cosmetic science

Challis BC, Trew DF, Guthrie WG, Roper DV.
PMID: 19245496
Int J Cosmet Sci. 1995 Jun;17(3):119-31. doi: 10.1111/j.1467-2494.1995.tb00115.x.

Summary From initial rate studies of morpholine nitrosation in aqueous media by nitrite ion in the presence of formaldehyde at pH 5-7 and 25 degrees C, four potential pathways are revealed for the concurrent formation of nitrosamine contaminants in...

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Challis BC, Trew DF, Guthrie WG, et al. Reduction of nitrosamines in cosmetic products. Int J Cosmet Sci. 1995;17(3):119-31doi: 10.1111/j.1467-2494.1995.tb00115.x.
Challis, B. C., Trew, D. F., Guthrie, W. G., & Roper, D. V. (1995). Reduction of nitrosamines in cosmetic products. International journal of cosmetic science, 17(3), 119-31. https://doi.org/10.1111/j.1467-2494.1995.tb00115.x
Challis, B C, et al. "Reduction of nitrosamines in cosmetic products." International journal of cosmetic science vol. 17,3 (1995): 119-31. doi: https://doi.org/10.1111/j.1467-2494.1995.tb00115.x
Challis BC, Trew DF, Guthrie WG, Roper DV. Reduction of nitrosamines in cosmetic products. Int J Cosmet Sci. 1995 Jun;17(3):119-31. doi: 10.1111/j.1467-2494.1995.tb00115.x. PMID: 19245496.
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Dioxazaborocanes: old adducts, new tricks.

Organic & biomolecular chemistry

Bonin H, Delacroix T, Gras E.
PMID: 21537514
Org Biomol Chem. 2011 Jul 07;9(13):4714-24. doi: 10.1039/c1ob05330b. Epub 2011 May 03.

Dioxazaborocanes are boronic adducts obtained by condensation of diethanolamine derivatives with boronic compounds. They were first described in the mid-1950's as a practical way to isolate a boronic adduct. Their use has for a long time been restricted to...

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Bonin H, Delacroix T, Gras E. Dioxazaborocanes: old adducts, new tricks. Org Biomol Chem. 2011;9(13):4714-24doi: 10.1039/c1ob05330b.
Bonin, H., Delacroix, T., & Gras, E. (2011). Dioxazaborocanes: old adducts, new tricks. Organic & biomolecular chemistry, 9(13), 4714-24. https://doi.org/10.1039/c1ob05330b
Bonin, Hélène, et al. "Dioxazaborocanes: old adducts, new tricks." Organic & biomolecular chemistry vol. 9,13 (2011): 4714-24. doi: https://doi.org/10.1039/c1ob05330b
Bonin H, Delacroix T, Gras E. Dioxazaborocanes: old adducts, new tricks. Org Biomol Chem. 2011 Jul 07;9(13):4714-24. doi: 10.1039/c1ob05330b. Epub 2011 May 03. PMID: 21537514.
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Showing 1 to 12 of 128 entries