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Psychiatric conditions and general practitioner attendance prior to HPV vaccination and the risk of referral to a specialized hospital setting because of suspected adverse events following HPV vaccination: a register-based, matched case-control study.

Clinical epidemiology

Lützen TH, Bech BH, Mehlsen J, Høstrup Vestergaard C, Krogsgaard LW, Olsen J, Vestergaard M, Plana-Ripoll O, Rytter D.
PMID: 28979164
Clin Epidemiol. 2017 Sep 12;9:465-473. doi: 10.2147/CLEP.S135318. eCollection 2017.

AIM: No association between human papilloma virus (HPV) vaccination and numerous diseases has been found. Still, a large number of Danish women are reporting suspected adverse events. Other factors may play a role, and the aim of this study...

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Lützen TH, Bech BH, Mehlsen J, et al. Psychiatric conditions and general practitioner attendance prior to HPV vaccination and the risk of referral to a specialized hospital setting because of suspected adverse events following HPV vaccination: a register-based, matched case-control study. Clin Epidemiol. 2017;9:465-473doi: 10.2147/CLEP.S135318.
Lützen, T. H., Bech, B. H., Mehlsen, J., Høstrup Vestergaard, C., Krogsgaard, L. W., Olsen, J., Vestergaard, M., Plana-Ripoll, O., & Rytter, D. (2017). Psychiatric conditions and general practitioner attendance prior to HPV vaccination and the risk of referral to a specialized hospital setting because of suspected adverse events following HPV vaccination: a register-based, matched case-control study. Clinical epidemiology, 9465-473. https://doi.org/10.2147/CLEP.S135318
Lützen, Tina Hovgaard, et al. "Psychiatric conditions and general practitioner attendance prior to HPV vaccination and the risk of referral to a specialized hospital setting because of suspected adverse events following HPV vaccination: a register-based, matched case-control study." Clinical epidemiology vol. 9 (2017): 465-473. doi: https://doi.org/10.2147/CLEP.S135318
Lützen TH, Bech BH, Mehlsen J, Høstrup Vestergaard C, Krogsgaard LW, Olsen J, Vestergaard M, Plana-Ripoll O, Rytter D. Psychiatric conditions and general practitioner attendance prior to HPV vaccination and the risk of referral to a specialized hospital setting because of suspected adverse events following HPV vaccination: a register-based, matched case-control study. Clin Epidemiol. 2017 Sep 12;9:465-473. doi: 10.2147/CLEP.S135318. eCollection 2017. PMID: 28979164; PMCID: PMC5602377.
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Self-assembly of heteroleptic dinuclear metallosupramolecular kites from multivalent ligands via social self-sorting.

Beilstein journal of organic chemistry

Benkhäuser C, Lützen A.
PMID: 26124873
Beilstein J Org Chem. 2015 May 08;11:693-700. doi: 10.3762/bjoc.11.79. eCollection 2015.

A Tröger's base-derived racemic bis(1,10-phenanthroline) ligand (rac)-1 and a bis(2,2'-bipyridine) ligand with a central 1,3-diethynylbenzene unit 2 were synthesized. Each of these ligands acts as a multivalent entity for the binding of two copper(I) ions. Upon coordination to the...

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Benkhäuser C, Lützen A. Self-assembly of heteroleptic dinuclear metallosupramolecular kites from multivalent ligands via social self-sorting. Beilstein J Org Chem. 2015;11:693-700doi: 10.3762/bjoc.11.79.
Benkhäuser, C., & Lützen, A. (2015). Self-assembly of heteroleptic dinuclear metallosupramolecular kites from multivalent ligands via social self-sorting. Beilstein journal of organic chemistry, 11693-700. https://doi.org/10.3762/bjoc.11.79
Benkhäuser, Christian, and Lützen, Arne. "Self-assembly of heteroleptic dinuclear metallosupramolecular kites from multivalent ligands via social self-sorting." Beilstein journal of organic chemistry vol. 11 (2015): 693-700. doi: https://doi.org/10.3762/bjoc.11.79
Benkhäuser C, Lützen A. Self-assembly of heteroleptic dinuclear metallosupramolecular kites from multivalent ligands via social self-sorting. Beilstein J Org Chem. 2015 May 08;11:693-700. doi: 10.3762/bjoc.11.79. eCollection 2015. PMID: 26124873; PMCID: PMC4464459.
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Interspecific hybridization among cultivars of hardy Hibiscus species section Muenchhusia.

Breeding science

Kuligowska K, Lütken H, Christensen B, Müller R.
PMID: 27162501
Breed Sci. 2016 Mar;66(2):300-8. doi: 10.1270/jsbbs.66.300. Epub 2016 Mar 01.

Rose mallows belong to the Muenchhusia section of the Hibiscus genus. They represent a small group of cold tolerant North American plants and are popular ornamentals mainly because of their abundant, large and colorful flowers. Due to their geographical...

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Kuligowska K, Lütken H, Christensen B, et al. Interspecific hybridization among cultivars of hardy Hibiscus species section Muenchhusia. Breed Sci. 2016;66(2):300-8doi: 10.1270/jsbbs.66.300.
Kuligowska, K., Lütken, H., Christensen, B., & Müller, R. (2016). Interspecific hybridization among cultivars of hardy Hibiscus species section Muenchhusia. Breeding science, 66(2), 300-8. https://doi.org/10.1270/jsbbs.66.300
Kuligowska, Katarzyna, et al. "Interspecific hybridization among cultivars of hardy Hibiscus species section Muenchhusia." Breeding science vol. 66,2 (2016): 300-8. doi: https://doi.org/10.1270/jsbbs.66.300
Kuligowska K, Lütken H, Christensen B, Müller R. Interspecific hybridization among cultivars of hardy Hibiscus species section Muenchhusia. Breed Sci. 2016 Mar;66(2):300-8. doi: 10.1270/jsbbs.66.300. Epub 2016 Mar 01. PMID: 27162501; PMCID: PMC4785007.
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Enantiomerically pure trinuclear helicates via diastereoselective self-assembly and characterization of their redox chemistry.

Journal of the American Chemical Society

Gütz C, Hovorka R, Struch N, Bunzen J, Meyer-Eppler G, Qu ZW, Grimme S, Topić F, Rissanen K, Cetina M, Engeser M, Lützen A.
PMID: 25050629
J Am Chem Soc. 2014 Aug 20;136(33):11830-8. doi: 10.1021/ja506327c. Epub 2014 Aug 05.

A tris(bipyridine) ligand 1 with two BINOL (BINOL = 2,2'-dihydroxy-1,1'-binaphthyl) groups has been prepared in two enantiomerically pure forms. This ligand undergoes completely diastereoselective self-assembly into D2-symmeteric double-stranded trinuclear helicates upon coordination to copper(I) and silver(I) ions and to...

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Gütz C, Hovorka R, Struch N, et al. Enantiomerically pure trinuclear helicates via diastereoselective self-assembly and characterization of their redox chemistry. J Am Chem Soc. 2014;136(33):11830-8doi: 10.1021/ja506327c.
Gütz, C., Hovorka, R., Struch, N., Bunzen, J., Meyer-Eppler, G., Qu, Z. W., Grimme, S., Topić, F., Rissanen, K., Cetina, M., Engeser, M., & Lützen, A. (2014). Enantiomerically pure trinuclear helicates via diastereoselective self-assembly and characterization of their redox chemistry. Journal of the American Chemical Society, 136(33), 11830-8. https://doi.org/10.1021/ja506327c
Gütz, Christoph, et al. "Enantiomerically pure trinuclear helicates via diastereoselective self-assembly and characterization of their redox chemistry." Journal of the American Chemical Society vol. 136,33 (2014): 11830-8. doi: https://doi.org/10.1021/ja506327c
Gütz C, Hovorka R, Struch N, Bunzen J, Meyer-Eppler G, Qu ZW, Grimme S, Topić F, Rissanen K, Cetina M, Engeser M, Lützen A. Enantiomerically pure trinuclear helicates via diastereoselective self-assembly and characterization of their redox chemistry. J Am Chem Soc. 2014 Aug 20;136(33):11830-8. doi: 10.1021/ja506327c. Epub 2014 Aug 05. PMID: 25050629.
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Patents and literature.

Applied biochemistry and biotechnology

Smith JA, Luenser SJ, Olson NF, Magee EL, Olivieri R, Viglia A, Degen L, Angelini L, Fascetti E, Miwa N, Masuda Y, Kawarabuki S, Sai T, Saito T, Busby MG, Hartwig DW, Heady R, Yagi Y, Kouno K, Inui T, Marshall JJ, Thomson AR, Miles BJ, Caygill JC, Moore DJ, Nakamura K, Nankai S, Iijima T, Ooshima Y, Baldeschwieler JD, Gamble RC, Mauk MR, Shen TY, Ponpipom MM, Khachatourians GG, Zaffaroni P, Senni A, Formiconi L, Blair JE, Davis LT, Cabane B, Vergnault J, Volesky B, Tsezos M, Bull FG, Messing RA, Ahnell JE, Chen LF, Gong CS, Tsao GT, Katsumata R, Green S, Leiser RS, Fedde PA, Ghosh S, Henry MP, Klass DL, Uemura Y, Arimura H, Morise H, Funakoshi S, Suyama T, Lützen NW, Kita DA, Fenton DM, Maclennan DG, Ousby JC, Owen TR, Steer DC, Araujo FJ, Calderon IL, Diaz IL, Olmedo C, Rebeller M, Yout P, Lonchamp D, Mynatt RL, Berg A, Eckmayer Z, Maselli JA, Horwath RO, Gotou E, Satou K, Wu RJ, Bahl CP, Narang SA, Hershberger CL, Baxter JD, Roberts JL, Seeburg PH, Goodman HM, Tsuchida T.
PMID: 24234462
Appl Biochem Biotechnol. 1982 Nov;7(6):497-510. doi: 10.1007/BF02799180.

No abstract available.

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Smith JA, Luenser SJ, Olson NF, et al. Patents and literature. Appl Biochem Biotechnol. 1982;7(6):497-510doi: 10.1007/BF02799180.
Smith, J. A., Luenser, S. J., Olson, N. F., Magee, E. L., Olivieri, R., Viglia, A., Degen, L., Angelini, L., Fascetti, E., Miwa, N., Masuda, Y., Kawarabuki, S., Sai, T., Saito, T., Busby, M. G., Hartwig, D. W., Heady, R., Yagi, Y., Kouno, K., Inui, T., Marshall, J. J., Thomson, A. R., Miles, B. J., Caygill, J. C., Moore, D. J., Nakamura, K., Nankai, S., Iijima, T., Ooshima, Y., Baldeschwieler, J. D., Gamble, R. C., Mauk, M. R., Shen, T. Y., Ponpipom, M. M., Khachatourians, G. G., Zaffaroni, P., Senni, A., Formiconi, L., Blair, J. E., Davis, L. T., Cabane, B., Vergnault, J., Volesky, B., Tsezos, M., Bull, F. G., Messing, R. A., Ahnell, J. E., Chen, L. F., Gong, C. S., Tsao, G. T., Katsumata, R., Green, S., Leiser, R. S., Fedde, P. A., Ghosh, S., Henry, M. P., Klass, D. L., Uemura, Y., Arimura, H., Morise, H., Funakoshi, S., Suyama, T., Lützen, N. W., Kita, D. A., Fenton, D. M., Maclennan, D. G., Ousby, J. C., Owen, T. R., Steer, D. C., Araujo, F. J., Calderon, I. L., Diaz, I. L., Olmedo, C., Rebeller, M., Yout, P., Lonchamp, D., Mynatt, R. L., Berg, A., Eckmayer, Z., Maselli, J. A., Horwath, R. O., Gotou, E., Satou, K., Wu, R. J., Bahl, C. P., Narang, S. A., Hershberger, C. L., Baxter, J. D., Roberts, J. L., Seeburg, P. H., Goodman, H. M., & Tsuchida, T. (1982). Patents and literature. Applied biochemistry and biotechnology, 7(6), 497-510. https://doi.org/10.1007/BF02799180
Smith, J A, et al. "Patents and literature." Applied biochemistry and biotechnology vol. 7,6 (1982): 497-510. doi: https://doi.org/10.1007/BF02799180
Smith JA, Luenser SJ, Olson NF, Magee EL, Olivieri R, Viglia A, Degen L, Angelini L, Fascetti E, Miwa N, Masuda Y, Kawarabuki S, Sai T, Saito T, Busby MG, Hartwig DW, Heady R, Yagi Y, Kouno K, Inui T, Marshall JJ, Thomson AR, Miles BJ, Caygill JC, Moore DJ, Nakamura K, Nankai S, Iijima T, Ooshima Y, Baldeschwieler JD, Gamble RC, Mauk MR, Shen TY, Ponpipom MM, Khachatourians GG, Zaffaroni P, Senni A, Formiconi L, Blair JE, Davis LT, Cabane B, Vergnault J, Volesky B, Tsezos M, Bull FG, Messing RA, Ahnell JE, Chen LF, Gong CS, Tsao GT, Katsumata R, Green S, Leiser RS, Fedde PA, Ghosh S, Henry MP, Klass DL, Uemura Y, Arimura H, Morise H, Funakoshi S, Suyama T, Lützen NW, Kita DA, Fenton DM, Maclennan DG, Ousby JC, Owen TR, Steer DC, Araujo FJ, Calderon IL, Diaz IL, Olmedo C, Rebeller M, Yout P, Lonchamp D, Mynatt RL, Berg A, Eckmayer Z, Maselli JA, Horwath RO, Gotou E, Satou K, Wu RJ, Bahl CP, Narang SA, Hershberger CL, Baxter JD, Roberts JL, Seeburg PH, Goodman HM, Tsuchida T. Patents and literature. Appl Biochem Biotechnol. 1982 Nov;7(6):497-510. doi: 10.1007/BF02799180. PMID: 24234462.
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Two New Carbaalanes: Compounds with an Al(7)C(5) and a.

Angewandte Chemie (International ed. in English)

Uhl W, Breher F, Lützen A, Saak W.
PMID: 10649427
Angew Chem Int Ed Engl. 2000 Jan;39(2):406-409.

The hydroalumination of aluminum ethynides leads to the formation of carbaalanes as a new class of compounds, which have clusters exclusively formed by carbon and aluminum atoms. Two novel carbaalanes with Al(7)C(5) and Al(7)C(4) clusters are described-the latter is...

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Uhl W, Breher F, Lützen A, et al. Two New Carbaalanes: Compounds with an Al(7)C(5) and a. Angew Chem Int Ed Engl. 2000;39(2):406-409
Uhl, W., Breher, F., Lützen, A., & Saak, W. (2000). Two New Carbaalanes: Compounds with an Al(7)C(5) and a. Angewandte Chemie (International ed. in English), 39(2), 406-409.
Uhl, et al. "Two New Carbaalanes: Compounds with an Al(7)C(5) and a." Angewandte Chemie (International ed. in English) vol. 39,2 (2000): 406-409.
Uhl W, Breher F, Lützen A, Saak W. Two New Carbaalanes: Compounds with an Al(7)C(5) and a. Angew Chem Int Ed Engl. 2000 Jan;39(2):406-409. PMID: 10649427.
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Developmental regulation of H+-ATPase-dependent auxin responses in the diageotropica mutant of tomato (Lycopersicon esculentum).

Physiologia plantarum

Coenen C, Bierfreund N, Lüthen H, Neuhaus G.
PMID: 12060269
Physiol Plant. 2002 Mar;114(3):461-471. doi: 10.1034/j.1399-3054.2002.1140316.x.

Rapid auxin effects on H+ pumping across the plasma membrane precede auxin-induced elongation growth of hypocotyls and swelling of guard cells, as well as auxin inhibition of root growth. To investigate whether auxin-signalling mechanisms in such diverse cell types...

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Coenen C, Bierfreund N, Lüthen H, et al. Developmental regulation of H+-ATPase-dependent auxin responses in the diageotropica mutant of tomato (Lycopersicon esculentum). Physiol Plant. 2002;114(3):461-471doi: 10.1034/j.1399-3054.2002.1140316.x.
Coenen, C., Bierfreund, N., Lüthen, H., & Neuhaus, G. (2002). Developmental regulation of H+-ATPase-dependent auxin responses in the diageotropica mutant of tomato (Lycopersicon esculentum). Physiologia plantarum, 114(3), 461-471. https://doi.org/10.1034/j.1399-3054.2002.1140316.x
Coenen, Catharina, et al. "Developmental regulation of H+-ATPase-dependent auxin responses in the diageotropica mutant of tomato (Lycopersicon esculentum)." Physiologia plantarum vol. 114,3 (2002): 461-471. doi: https://doi.org/10.1034/j.1399-3054.2002.1140316.x
Coenen C, Bierfreund N, Lüthen H, Neuhaus G. Developmental regulation of H+-ATPase-dependent auxin responses in the diageotropica mutant of tomato (Lycopersicon esculentum). Physiol Plant. 2002 Mar;114(3):461-471. doi: 10.1034/j.1399-3054.2002.1140316.x. PMID: 12060269.
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Reexamination of the Acid growth theory of auxin action.

Plant physiology

Lüthen H, Bigdon M, Böttger M.
PMID: 16667603
Plant Physiol. 1990 Jul;93(3):931-9. doi: 10.1104/pp.93.3.931.

Some crucial arguments against the acid growth theory of auxin action (U Kutschera, P Schopfer [1985] Planta 163: 483-493) have been reinvestigated by simultaneous measurements of proton fluxes and growth of maize (Zea mays L.) coleoptiles. Special care was...

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Lüthen H, Bigdon M, Böttger M. Reexamination of the Acid growth theory of auxin action. Plant Physiol. 1990;93(3):931-9doi: 10.1104/pp.93.3.931.
Lüthen, H., Bigdon, M., & Böttger, M. (1990). Reexamination of the Acid growth theory of auxin action. Plant physiology, 93(3), 931-9. https://doi.org/10.1104/pp.93.3.931
Lüthen, H, et al. "Reexamination of the Acid growth theory of auxin action." Plant physiology vol. 93,3 (1990): 931-9. doi: https://doi.org/10.1104/pp.93.3.931
Lüthen H, Bigdon M, Böttger M. Reexamination of the Acid growth theory of auxin action. Plant Physiol. 1990 Jul;93(3):931-9. doi: 10.1104/pp.93.3.931. PMID: 16667603; PMCID: PMC1062611.
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Self-discriminating self-assembly of dinuclear heterochiral rhombs from Tröger's base derived bis(pyridyl) ligands.

Chemistry (Weinheim an der Bergstrasse, Germany)

Weilandt T, Kiehne U, Bunzen J, Schnakenburg G, Lützen A.
PMID: 20077545
Chemistry. 2010 Feb 22;16(8):2418-26. doi: 10.1002/chem.200902993.

Five racemic dissymmetric bis(pyridyl) ligands based on 2,8- or 3,9-difunctionalised Tröger's base derivatives have been synthesised. Only those derived from a 2,8-difunctionalised scaffold were found to undergo selective self-assembly to discrete self-assembled dinuclear metallosupramolecular aggregates of rhomboid shape upon...

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Weilandt T, Kiehne U, Bunzen J, et al. Self-discriminating self-assembly of dinuclear heterochiral rhombs from Tröger's base derived bis(pyridyl) ligands. Chemistry. 2010;16(8):2418-26doi: 10.1002/chem.200902993.
Weilandt, T., Kiehne, U., Bunzen, J., Schnakenburg, G., & Lützen, A. (2010). Self-discriminating self-assembly of dinuclear heterochiral rhombs from Tröger's base derived bis(pyridyl) ligands. Chemistry (Weinheim an der Bergstrasse, Germany), 16(8), 2418-26. https://doi.org/10.1002/chem.200902993
Weilandt, Torsten, et al. "Self-discriminating self-assembly of dinuclear heterochiral rhombs from Tröger's base derived bis(pyridyl) ligands." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 16,8 (2010): 2418-26. doi: https://doi.org/10.1002/chem.200902993
Weilandt T, Kiehne U, Bunzen J, Schnakenburg G, Lützen A. Self-discriminating self-assembly of dinuclear heterochiral rhombs from Tröger's base derived bis(pyridyl) ligands. Chemistry. 2010 Feb 22;16(8):2418-26. doi: 10.1002/chem.200902993. PMID: 20077545.
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A new structural motif for an enantiomerically pure metallosupramolecular Pd₄L₈ aggregate by anion templating.

Angewandte Chemie (International ed. in English)

Klein C, Gütz C, Bogner M, Topić F, Rissanen K, Lützen A.
PMID: 24590898
Angew Chem Int Ed Engl. 2014 Apr 01;53(14):3739-42. doi: 10.1002/anie.201400626. Epub 2014 Mar 03.

An enantiomerically pure BINOL-based bis(3-pyridyl) ligand 1 assembles into a homochiral [Pd4(1)8] complex upon coordination to tetravalent Pd(II) ions. The formation of this aggregate is templated by two tetrafluoroborate counterions that are encapsulated in two peripheral cavities. The resulting...

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Klein C, Gütz C, Bogner M, et al. A new structural motif for an enantiomerically pure metallosupramolecular Pd₄L₈ aggregate by anion templating. Angew Chem Int Ed Engl. 2014;53(14):3739-42doi: 10.1002/anie.201400626.
Klein, C., Gütz, C., Bogner, M., Topić, F., Rissanen, K., & Lützen, A. (2014). A new structural motif for an enantiomerically pure metallosupramolecular Pd₄L₈ aggregate by anion templating. Angewandte Chemie (International ed. in English), 53(14), 3739-42. https://doi.org/10.1002/anie.201400626
Klein, Christoph, et al. "A new structural motif for an enantiomerically pure metallosupramolecular Pd₄L₈ aggregate by anion templating." Angewandte Chemie (International ed. in English) vol. 53,14 (2014): 3739-42. doi: https://doi.org/10.1002/anie.201400626
Klein C, Gütz C, Bogner M, Topić F, Rissanen K, Lützen A. A new structural motif for an enantiomerically pure metallosupramolecular Pd₄L₈ aggregate by anion templating. Angew Chem Int Ed Engl. 2014 Apr 01;53(14):3739-42. doi: 10.1002/anie.201400626. Epub 2014 Mar 03. PMID: 24590898.
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Molecular recognition of isomeric protonated amino acid esters monitored by ESI-mass spectrometry.

Beilstein journal of organic chemistry

Liesenfeld A, Lützen A.
PMID: 24778737
Beilstein J Org Chem. 2014 Apr 09;10:825-31. doi: 10.3762/bjoc.10.78. eCollection 2014.

Two new 9,9'-spirobifluorene-derived crown ethers were prepared and used to recognise constitutionally isomeric amino acid derivatives. The performance of the receptors was evaluated by ESI-mass spectrometry using the isomer labelled guest method (ILGM). This method revealed the preferred binding...

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Liesenfeld A, Lützen A. Molecular recognition of isomeric protonated amino acid esters monitored by ESI-mass spectrometry. Beilstein J Org Chem. 2014;10:825-31doi: 10.3762/bjoc.10.78.
Liesenfeld, A., & Lützen, A. (2014). Molecular recognition of isomeric protonated amino acid esters monitored by ESI-mass spectrometry. Beilstein journal of organic chemistry, 10825-31. https://doi.org/10.3762/bjoc.10.78
Liesenfeld, Andrea, and Lützen, Arne. "Molecular recognition of isomeric protonated amino acid esters monitored by ESI-mass spectrometry." Beilstein journal of organic chemistry vol. 10 (2014): 825-31. doi: https://doi.org/10.3762/bjoc.10.78
Liesenfeld A, Lützen A. Molecular recognition of isomeric protonated amino acid esters monitored by ESI-mass spectrometry. Beilstein J Org Chem. 2014 Apr 09;10:825-31. doi: 10.3762/bjoc.10.78. eCollection 2014. PMID: 24778737; PMCID: PMC3999762.
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Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a,e]cyclooctatetraenes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Melcher MC, Ivšić T, Olagnon C, Tenten C, Lützen A, Strand D.
PMID: 29131428
Chemistry. 2018 Feb 16;24(10):2344-2348. doi: 10.1002/chem.201704816. Epub 2017 Dec 14.

Planar chiral 5,11-disubstiuted dibenzo[a,e]cyclo-octatetraenes (dbCOTs) have been developed as the first useful chiral homologs to dbCOT-ligands for asymmetric applications. Methods enabling the preparation of such compounds on a gram-scale in enantiomerically pure form are described. Evaluated as ligands in...

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Melcher MC, Ivšić T, Olagnon C, et al. Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a,e]cyclooctatetraenes. Chemistry. 2017;24(10):2344-2348doi: 10.1002/chem.201704816.
Melcher, M. C., Ivšić, T., Olagnon, C., Tenten, C., Lützen, A., & Strand, D. (2018). Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a,e]cyclooctatetraenes. Chemistry (Weinheim an der Bergstrasse, Germany), 24(10), 2344-2348. https://doi.org/10.1002/chem.201704816
Melcher, Michaela-Christina, et al. "Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a,e]cyclooctatetraenes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 24,10 (2018): 2344-2348. doi: https://doi.org/10.1002/chem.201704816
Melcher MC, Ivšić T, Olagnon C, Tenten C, Lützen A, Strand D. Control of Enantioselectivity in Rhodium(I) Catalysis by Planar Chiral Dibenzo[a,e]cyclooctatetraenes. Chemistry. 2018 Feb 16;24(10):2344-2348. doi: 10.1002/chem.201704816. Epub 2017 Dec 14. PMID: 29131428.
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Showing 1 to 12 of 88 entries