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A comparative study of two polymorphs of bis(1-hydroxy-2-methylpropan-2-aminium) carbonate.

Acta crystallographica. Section C, Structural chemistry

Ben Nasr M, Aubert E, Espinosa E.
PMID: 26942432
Acta Crystallogr C Struct Chem. 2016 Mar;72:225-9. doi: 10.1107/S2053229616002849. Epub 2016 Feb 24.

Alkanolamines have been known for their high CO2 absorption for over 60 years and are used widely in the natural gas industry for reversible CO2 capture. In an attempt to crystallize a salt of (RS)-2-(3-benzoylphenyl)propionic acid with 2-amino-2-methylpropan-1-ol, we...

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Ben Nasr M, Aubert E, Espinosa E. A comparative study of two polymorphs of bis(1-hydroxy-2-methylpropan-2-aminium) carbonate. Acta Crystallogr C Struct Chem. 2016;72:225-9doi: 10.1107/S2053229616002849.
Ben Nasr, M., Aubert, E., & Espinosa, E. (2016). A comparative study of two polymorphs of bis(1-hydroxy-2-methylpropan-2-aminium) carbonate. Acta crystallographica. Section C, Structural chemistry, 72225-9. https://doi.org/10.1107/S2053229616002849
Ben Nasr, Mahjouba, et al. "A comparative study of two polymorphs of bis(1-hydroxy-2-methylpropan-2-aminium) carbonate." Acta crystallographica. Section C, Structural chemistry vol. 72 (2016): 225-9. doi: https://doi.org/10.1107/S2053229616002849
Ben Nasr M, Aubert E, Espinosa E. A comparative study of two polymorphs of bis(1-hydroxy-2-methylpropan-2-aminium) carbonate. Acta Crystallogr C Struct Chem. 2016 Mar;72:225-9. doi: 10.1107/S2053229616002849. Epub 2016 Feb 24. PMID: 26942432.
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Inter-layer charge disproportionation in the dual-layer organic metal (tTTF-I)2ClO4 with unsymmetrical I···O halogen bond interactions.

Dalton transactions (Cambridge, England : 2003)

Shin KS, Jeannin O, Brezgunova M, Dahaoui S, Aubert E, Espinosa E, Auban-Senzier P, Świetlik R, Frąckowiak A, Fourmigué M.
PMID: 24327264
Dalton Trans. 2014 Apr 14;43(14):5280-91. doi: 10.1039/c3dt52801d.

A mixed-valence salt of tTTF-I with ClO4(-), formulated as (tTTF-I)2ClO4, is characterized by the presence of two crystallographically independent donor molecules, segregated in different layers and linked together through I···O interactions with the ClO4(-) anion disordered at room temperature....

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Shin KS, Jeannin O, Brezgunova M, et al. Inter-layer charge disproportionation in the dual-layer organic metal (tTTF-I)2ClO4 with unsymmetrical I···O halogen bond interactions. Dalton Trans. 2014;43(14):5280-91doi: 10.1039/c3dt52801d.
Shin, K. S., Jeannin, O., Brezgunova, M., Dahaoui, S., Aubert, E., Espinosa, E., Auban-Senzier, P., Świetlik, R., Frąckowiak, A., & Fourmigué, M. (2014). Inter-layer charge disproportionation in the dual-layer organic metal (tTTF-I)2ClO4 with unsymmetrical I···O halogen bond interactions. Dalton transactions (Cambridge, England : 2003), 43(14), 5280-91. https://doi.org/10.1039/c3dt52801d
Shin, Kyoung-Soon, et al. "Inter-layer charge disproportionation in the dual-layer organic metal (tTTF-I)2ClO4 with unsymmetrical I···O halogen bond interactions." Dalton transactions (Cambridge, England : 2003) vol. 43,14 (2014): 5280-91. doi: https://doi.org/10.1039/c3dt52801d
Shin KS, Jeannin O, Brezgunova M, Dahaoui S, Aubert E, Espinosa E, Auban-Senzier P, Świetlik R, Frąckowiak A, Fourmigué M. Inter-layer charge disproportionation in the dual-layer organic metal (tTTF-I)2ClO4 with unsymmetrical I···O halogen bond interactions. Dalton Trans. 2014 Apr 14;43(14):5280-91. doi: 10.1039/c3dt52801d. PMID: 24327264.
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Prognostic value of FDG PET/CT in head and neck squamous cell carcinomas.

OncoTargets and therapy

Dequanter D, Shahla M, Aubert C, Deniz Y, Lothaire P.
PMID: 26346890
Onco Targets Ther. 2015 Aug 26;8:2279-83. doi: 10.2147/OTT.S85479. eCollection 2015.

INTRODUCTION: The purpose of this study was to evaluate the use of (18)F-fluorodeoxyglucose positron emission tomography/computed tomography ((18)F-FDG PET/CT) to identify the presence of cervical lymph nodes metastases and extracapsular spread with histologic correlations in head and neck squamous...

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Dequanter D, Shahla M, Aubert C, et al. Prognostic value of FDG PET/CT in head and neck squamous cell carcinomas. Onco Targets Ther. 2015;8:2279-83doi: 10.2147/OTT.S85479.
Dequanter, D., Shahla, M., Aubert, C., Deniz, Y., & Lothaire, P. (2015). Prognostic value of FDG PET/CT in head and neck squamous cell carcinomas. OncoTargets and therapy, 82279-83. https://doi.org/10.2147/OTT.S85479
Dequanter, D, et al. "Prognostic value of FDG PET/CT in head and neck squamous cell carcinomas." OncoTargets and therapy vol. 8 (2015): 2279-83. doi: https://doi.org/10.2147/OTT.S85479
Dequanter D, Shahla M, Aubert C, Deniz Y, Lothaire P. Prognostic value of FDG PET/CT in head and neck squamous cell carcinomas. Onco Targets Ther. 2015 Aug 26;8:2279-83. doi: 10.2147/OTT.S85479. eCollection 2015. PMID: 26346890; PMCID: PMC4556030.
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Double-Stereodifferentiation in Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition: Chiral Ligand/Chiral Counterion Matched Pair.

Organic letters

Augé M, Feraldi-Xypolia A, Barbazanges M, Aubert C, Fensterbank L, Gandon V, Kolodziej E, Ollivier C.
PMID: 26219218
Org Lett. 2015 Aug 07;17(15):3754-7. doi: 10.1021/acs.orglett.5b01738. Epub 2015 Jul 29.

The first enantioselective metal-catalyzed [2 + 2 + 2] cycloaddition involving a double asymmetric induction has been devised. It relies on the use of an in situ generated chiral cationic rhodium(I) catalyst with a matched chiral ligand/chiral counterion pair....

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Augé M, Feraldi-Xypolia A, Barbazanges M, et al. Double-Stereodifferentiation in Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition: Chiral Ligand/Chiral Counterion Matched Pair. Org Lett. 2015;17(15):3754-7doi: 10.1021/acs.orglett.5b01738.
Augé, M., Feraldi-Xypolia, A., Barbazanges, M., Aubert, C., Fensterbank, L., Gandon, V., Kolodziej, E., & Ollivier, C. (2015). Double-Stereodifferentiation in Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition: Chiral Ligand/Chiral Counterion Matched Pair. Organic letters, 17(15), 3754-7. https://doi.org/10.1021/acs.orglett.5b01738
Augé, Mylène, et al. "Double-Stereodifferentiation in Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition: Chiral Ligand/Chiral Counterion Matched Pair." Organic letters vol. 17,15 (2015): 3754-7. doi: https://doi.org/10.1021/acs.orglett.5b01738
Augé M, Feraldi-Xypolia A, Barbazanges M, Aubert C, Fensterbank L, Gandon V, Kolodziej E, Ollivier C. Double-Stereodifferentiation in Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition: Chiral Ligand/Chiral Counterion Matched Pair. Org Lett. 2015 Aug 07;17(15):3754-7. doi: 10.1021/acs.orglett.5b01738. Epub 2015 Jul 29. PMID: 26219218.
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Adiposity throughout adulthood and risk of sudden cardiac death in women.

JACC. Clinical electrophysiology

Chiuve SE, Sun Q, Sandhu RK, Tedrow U, Cook NR, Manson JE, Albert CM.
PMID: 26824079
JACC Clin Electrophysiol. 2015 Dec 01;1(6):520-528. doi: 10.1016/j.jacep.2015.07.011.

BACKGROUND: Sudden cardiac death (SCD) is often the first manifestation of coronary heart disease (CHD) among women. Data regarding BMI and risk of SCD are limited and conflicting.OBJECTIVES: We examined the association of BMI repeatedly measured over 32 years...

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Chiuve SE, Sun Q, Sandhu RK, et al. Adiposity throughout adulthood and risk of sudden cardiac death in women. JACC Clin Electrophysiol. 2015;1(6):520-528doi: 10.1016/j.jacep.2015.07.011.
Chiuve, S. E., Sun, Q., Sandhu, R. K., Tedrow, U., Cook, N. R., Manson, J. E., & Albert, C. M. (2015). Adiposity throughout adulthood and risk of sudden cardiac death in women. JACC. Clinical electrophysiology, 1(6), 520-528. https://doi.org/10.1016/j.jacep.2015.07.011
Chiuve, Stephanie E, et al. "Adiposity throughout adulthood and risk of sudden cardiac death in women." JACC. Clinical electrophysiology vol. 1,6 (2015): 520-528. doi: https://doi.org/10.1016/j.jacep.2015.07.011
Chiuve SE, Sun Q, Sandhu RK, Tedrow U, Cook NR, Manson JE, Albert CM. Adiposity throughout adulthood and risk of sudden cardiac death in women. JACC Clin Electrophysiol. 2015 Dec 01;1(6):520-528. doi: 10.1016/j.jacep.2015.07.011. PMID: 26824079; PMCID: PMC4725590.
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Poly[diaquatris(μ6-4,6-dioxo-1,4,5,6-tetra-hydro-1,3,5-triazine-2-carboxylato)tripotassium].

Acta crystallographica. Section E, Structure reports online

Soudani S, Aubert E, Wenger E, Jelsch C, Gautier-Luneau I, Ben Nasr C.
PMID: 24860308
Acta Crystallogr Sect E Struct Rep Online. 2014 Apr 09;70:m174-5. doi: 10.1107/S1600536814007569. eCollection 2014 May 01.

The asymmetric unit of the title compound, [K3(C4H2N3O4)3(H2O)2] n , contains two potassium cations (one in general position, one located on a twofold rotation axis), one and a half oxonate anions (the other half generated by twofold symmetry) and...

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Soudani S, Aubert E, Wenger E, et al. Poly[diaquatris(μ6-4,6-dioxo-1,4,5,6-tetra-hydro-1,3,5-triazine-2-carboxylato)tripotassium]. Acta Crystallogr Sect E Struct Rep Online. 2014;70:m174-5doi: 10.1107/S1600536814007569.
Soudani, S., Aubert, E., Wenger, E., Jelsch, C., Gautier-Luneau, I., & Ben Nasr, C. (2014). Poly[diaquatris(μ6-4,6-dioxo-1,4,5,6-tetra-hydro-1,3,5-triazine-2-carboxylato)tripotassium]. Acta crystallographica. Section E, Structure reports online, 70m174-5. https://doi.org/10.1107/S1600536814007569
Soudani, Sarra, et al. "Poly[diaquatris(μ6-4,6-dioxo-1,4,5,6-tetra-hydro-1,3,5-triazine-2-carboxylato)tripotassium]." Acta crystallographica. Section E, Structure reports online vol. 70 (2014): m174-5. doi: https://doi.org/10.1107/S1600536814007569
Soudani S, Aubert E, Wenger E, Jelsch C, Gautier-Luneau I, Ben Nasr C. Poly[diaquatris(μ6-4,6-dioxo-1,4,5,6-tetra-hydro-1,3,5-triazine-2-carboxylato)tripotassium]. Acta Crystallogr Sect E Struct Rep Online. 2014 Apr 09;70:m174-5. doi: 10.1107/S1600536814007569. eCollection 2014 May 01. PMID: 24860308; PMCID: PMC4011208.
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Mild niobium-catalyzed [2 + 2 + 2] cycloaddition of sila-triynes: easy access to polysubstituted benzosilacyclobutenes.

Organic letters

Simon C, Amatore M, Aubert C, Petit M.
PMID: 25668409
Org Lett. 2015 Feb 20;17(4):844-7. doi: 10.1021/ol503663k. Epub 2015 Feb 10.

A new and efficient synthesis of highly sensitive benzosilacyclobutenes has been developed. For the first time, these compounds can be synthesized in very high yields by a mild, unprecedented intramolecular niobium-catalyzed [2 + 2 + 2] cycloaddition of easily...

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Simon C, Amatore M, Aubert C, et al. Mild niobium-catalyzed [2 + 2 + 2] cycloaddition of sila-triynes: easy access to polysubstituted benzosilacyclobutenes. Org Lett. 2015;17(4):844-7doi: 10.1021/ol503663k.
Simon, C., Amatore, M., Aubert, C., & Petit, M. (2015). Mild niobium-catalyzed [2 + 2 + 2] cycloaddition of sila-triynes: easy access to polysubstituted benzosilacyclobutenes. Organic letters, 17(4), 844-7. https://doi.org/10.1021/ol503663k
Simon, Cédric, et al. "Mild niobium-catalyzed [2 + 2 + 2] cycloaddition of sila-triynes: easy access to polysubstituted benzosilacyclobutenes." Organic letters vol. 17,4 (2015): 844-7. doi: https://doi.org/10.1021/ol503663k
Simon C, Amatore M, Aubert C, Petit M. Mild niobium-catalyzed [2 + 2 + 2] cycloaddition of sila-triynes: easy access to polysubstituted benzosilacyclobutenes. Org Lett. 2015 Feb 20;17(4):844-7. doi: 10.1021/ol503663k. Epub 2015 Feb 10. PMID: 25668409.
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Cobalt(I)-mediated cycloisomerization of enynes: mechanistic insights.

Chemistry (Weinheim an der Bergstrasse, Germany)

Buisine O, Aubert C, Malacria M.
PMID: 11560322
Chemistry. 2001 Aug 17;7(16):3517-25. doi: 10.1002/1521-3765(20010817)7:16<3517::aid-chem3517>3.0.co;2-v.

[CpCo(CO)2] catalyzes the cycloisomerization of 1,n-enynes to afford selectively five- and six-membered ring systems in high yields. The factors governing the cyclization have been explored and we have discovered that the reaction associates two different, but complementary, reactivities of...

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Buisine O, Aubert C, Malacria M. Cobalt(I)-mediated cycloisomerization of enynes: mechanistic insights. Chemistry. 2001;7(16):3517-25doi: 10.1002/1521-3765(20010817)7:16<3517::aid-chem3517>3.0.co;2-v.
Buisine, O., Aubert, C., & Malacria, M. (2001). Cobalt(I)-mediated cycloisomerization of enynes: mechanistic insights. Chemistry (Weinheim an der Bergstrasse, Germany), 7(16), 3517-25. https://doi.org/10.1002/1521-3765(20010817)7:16<3517::aid-chem3517>3.0.co;2-v
Buisine, O, et al. "Cobalt(I)-mediated cycloisomerization of enynes: mechanistic insights." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 7,16 (2001): 3517-25. doi: https://doi.org/10.1002/1521-3765(20010817)7:16<3517::aid-chem3517>3.0.co;2-v
Buisine O, Aubert C, Malacria M. Cobalt(I)-mediated cycloisomerization of enynes: mechanistic insights. Chemistry. 2001 Aug 17;7(16):3517-25. doi: 10.1002/1521-3765(20010817)7:16<3517::aid-chem3517>3.0.co;2-v. PMID: 11560322.
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A multicenter study to assess outcome following a switch in the primary immunosuppressant from cyclosporin (CYA) to tacrolimus (TAC) in lung recipients.

The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation

Klepetko W, Estenne M, Glanville A, Verleden G, Aubert JD, Sarahrudi K, Gerbase M, Hirt S, Reichenspurner H, Ploner M.
PMID: 11250377
J Heart Lung Transplant. 2001 Feb;20(2):208. doi: 10.1016/s1053-2498(00)00448-4.

No abstract available.

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Klepetko W, Estenne M, Glanville A, et al. A multicenter study to assess outcome following a switch in the primary immunosuppressant from cyclosporin (CYA) to tacrolimus (TAC) in lung recipients. J Heart Lung Transplant. 2001;20(2):208doi: 10.1016/s1053-2498(00)00448-4.
Klepetko, W., Estenne, M., Glanville, A., Verleden, G., Aubert, J. D., Sarahrudi, K., Gerbase, M., Hirt, S., Reichenspurner, H., & Ploner, M. (2001). A multicenter study to assess outcome following a switch in the primary immunosuppressant from cyclosporin (CYA) to tacrolimus (TAC) in lung recipients. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 20(2), 208. https://doi.org/10.1016/s1053-2498(00)00448-4
Klepetko, W, et al. "A multicenter study to assess outcome following a switch in the primary immunosuppressant from cyclosporin (CYA) to tacrolimus (TAC) in lung recipients." The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation vol. 20,2 (2001): 208. doi: https://doi.org/10.1016/s1053-2498(00)00448-4
Klepetko W, Estenne M, Glanville A, Verleden G, Aubert JD, Sarahrudi K, Gerbase M, Hirt S, Reichenspurner H, Ploner M. A multicenter study to assess outcome following a switch in the primary immunosuppressant from cyclosporin (CYA) to tacrolimus (TAC) in lung recipients. J Heart Lung Transplant. 2001 Feb;20(2):208. doi: 10.1016/s1053-2498(00)00448-4. PMID: 11250377.
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Diastereoselective cobalt-mediated [2 + 2 + 2] cycloadditions of substituted linear enediynes phosphine oxides: scope and limitations.

The Journal of organic chemistry

Slowinski F, Aubert C, Malacria M.
PMID: 12530863
J Org Chem. 2003 Jan 24;68(2):378-86. doi: 10.1021/jo026212r.

Variously substituted linear enediynes phosphines oxides possessing the double bond at either the terminal or internal position and with the phosphine oxide appended onto the alkyne or the alkene terminus have been prepared. Their cobalt(I)-mediated cyclizations produce the eta(4)-complexed...

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Slowinski F, Aubert C, Malacria M. Diastereoselective cobalt-mediated [2 + 2 + 2] cycloadditions of substituted linear enediynes phosphine oxides: scope and limitations. J Org Chem. 2003;68(2):378-86doi: 10.1021/jo026212r.
Slowinski, F., Aubert, C., & Malacria, M. (2003). Diastereoselective cobalt-mediated [2 + 2 + 2] cycloadditions of substituted linear enediynes phosphine oxides: scope and limitations. The Journal of organic chemistry, 68(2), 378-86. https://doi.org/10.1021/jo026212r
Slowinski, Franck, et al. "Diastereoselective cobalt-mediated [2 + 2 + 2] cycloadditions of substituted linear enediynes phosphine oxides: scope and limitations." The Journal of organic chemistry vol. 68,2 (2003): 378-86. doi: https://doi.org/10.1021/jo026212r
Slowinski F, Aubert C, Malacria M. Diastereoselective cobalt-mediated [2 + 2 + 2] cycloadditions of substituted linear enediynes phosphine oxides: scope and limitations. J Org Chem. 2003 Jan 24;68(2):378-86. doi: 10.1021/jo026212r. PMID: 12530863.
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Long-range self-assembly of a polyunsaturated linear organosilane at the n-tetradecane/Au(111) interface studied by STM.

Journal of the American Chemical Society

Marchenko A, Katsonis N, Fichou D, Aubert C, Malacria M.
PMID: 12188658
J Am Chem Soc. 2002 Aug 28;124(34):9998-9. doi: 10.1021/ja027002z.

We report on the formation of self-assembled monolayers of 13-(trimethylsilyl)-1-tridecene-6,12-diyne [C13H17-Si(CH3)3], an organosilane derivative with a linear polyunsaturated chain, on Au(111) substrates. Molecular resolution STM images recorded at the liquid-solid interface between gold and tetradecane reveal a long-range and...

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Marchenko A, Katsonis N, Fichou D, et al. Long-range self-assembly of a polyunsaturated linear organosilane at the n-tetradecane/Au(111) interface studied by STM. J Am Chem Soc. 2002;124(34):9998-9doi: 10.1021/ja027002z.
Marchenko, A., Katsonis, N., Fichou, D., Aubert, C., & Malacria, M. (2002). Long-range self-assembly of a polyunsaturated linear organosilane at the n-tetradecane/Au(111) interface studied by STM. Journal of the American Chemical Society, 124(34), 9998-9. https://doi.org/10.1021/ja027002z
Marchenko, Alexandr, et al. "Long-range self-assembly of a polyunsaturated linear organosilane at the n-tetradecane/Au(111) interface studied by STM." Journal of the American Chemical Society vol. 124,34 (2002): 9998-9. doi: https://doi.org/10.1021/ja027002z
Marchenko A, Katsonis N, Fichou D, Aubert C, Malacria M. Long-range self-assembly of a polyunsaturated linear organosilane at the n-tetradecane/Au(111) interface studied by STM. J Am Chem Soc. 2002 Aug 28;124(34):9998-9. doi: 10.1021/ja027002z. PMID: 12188658.
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The behavior of 1,n-enynes in the presence of transition metals.

Chemical reviews

Aubert C, Buisine O, Malacria M.
PMID: 11890758
Chem Rev. 2002 Mar;102(3):813-34. doi: 10.1021/cr980054f.

No abstract available.

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Aubert C, Buisine O, Malacria M. The behavior of 1,n-enynes in the presence of transition metals. Chem Rev. 2002;102(3):813-34doi: 10.1021/cr980054f.
Aubert, C., Buisine, O., & Malacria, M. (2002). The behavior of 1,n-enynes in the presence of transition metals. Chemical reviews, 102(3), 813-34. https://doi.org/10.1021/cr980054f
Aubert, Corinne, et al. "The behavior of 1,n-enynes in the presence of transition metals." Chemical reviews vol. 102,3 (2002): 813-34. doi: https://doi.org/10.1021/cr980054f
Aubert C, Buisine O, Malacria M. The behavior of 1,n-enynes in the presence of transition metals. Chem Rev. 2002 Mar;102(3):813-34. doi: 10.1021/cr980054f. PMID: 11890758.
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Showing 1 to 12 of 259 entries