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A new polymer-attached reagent for the oxidation of primary and secondary alcohols.

Organic letters

Sourkouni-Argirusi G, Kirschning A.
PMID: 11101418
Org Lett. 2000 Nov 30;2(24):3781-4. doi: 10.1021/ol006483t.

A new, polymer-bound reagent system for the efficient oxidation of primary alcohols to aldehydes and secondary alcohols to ketones in the presence of a catalytic amount of 2,2,6, 6-tetramethyl-1-piperidinyloxyl (TEMPO) is described. In most cases, workup of this heavy...

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Sourkouni-Argirusi G, Kirschning A. A new polymer-attached reagent for the oxidation of primary and secondary alcohols. Org Lett. 2000;2(24):3781-4doi: 10.1021/ol006483t.
Sourkouni-Argirusi, G., & Kirschning, A. (2000). A new polymer-attached reagent for the oxidation of primary and secondary alcohols. Organic letters, 2(24), 3781-4. https://doi.org/10.1021/ol006483t
Sourkouni-Argirusi, and Kirschning. "A new polymer-attached reagent for the oxidation of primary and secondary alcohols." Organic letters vol. 2,24 (2000): 3781-4. doi: https://doi.org/10.1021/ol006483t
Sourkouni-Argirusi G, Kirschning A. A new polymer-attached reagent for the oxidation of primary and secondary alcohols. Org Lett. 2000 Nov 30;2(24):3781-4. doi: 10.1021/ol006483t. PMID: 11101418.
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Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons.

Angewandte Chemie (International ed. in English)

Luy B, Hauser G, Kirschning A, Glaser SJ.
PMID: 12645070
Angew Chem Int Ed Engl. 2003 Mar 17;42(11):1300-2. doi: 10.1002/anie.200390335.

No abstract available.

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Luy B, Hauser G, Kirschning A, et al. Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons. Angew Chem Int Ed Engl. 2003;42(11):1300-2doi: 10.1002/anie.200390335.
Luy, B., Hauser, G., Kirschning, A., & Glaser, S. J. (2003). Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons. Angewandte Chemie (International ed. in English), 42(11), 1300-2. https://doi.org/10.1002/anie.200390335
Luy, Burkhard, et al. "Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons." Angewandte Chemie (International ed. in English) vol. 42,11 (2003): 1300-2. doi: https://doi.org/10.1002/anie.200390335
Luy B, Hauser G, Kirschning A, Glaser SJ. Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons. Angew Chem Int Ed Engl. 2003 Mar 17;42(11):1300-2. doi: 10.1002/anie.200390335. PMID: 12645070.
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The influence of microgravity on the morphology of identified cerebral neurons in a cricket (Acheta domesticus).

Journal of gravitational physiology : a journal of the International Society for Gravitational Physiology

Kirschnik U, Horn E, Agricola HJ.
PMID: 14703671
J Gravit Physiol. 2002 Jul;9(1):P27-8.

Studies in cricket larvae (Acheta domesticus) revealed that descending sulfakinin-ir-neurons (PDS-neurons) from the sensorimotor area of the brain are insensitive to gravity deprivation if they were exposed to microgravity after determination of their shape. In the project CRISP-2, we...

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Kirschnik U, Horn E, Agricola HJ. The influence of microgravity on the morphology of identified cerebral neurons in a cricket (Acheta domesticus). J Gravit Physiol. 2002;9(1):P27-8
Kirschnik, U., Horn, E., & Agricola, H. J. (2002). The influence of microgravity on the morphology of identified cerebral neurons in a cricket (Acheta domesticus). Journal of gravitational physiology : a journal of the International Society for Gravitational Physiology, 9(1), P27-8.
Kirschnik, Uta, et al. "The influence of microgravity on the morphology of identified cerebral neurons in a cricket (Acheta domesticus)." Journal of gravitational physiology : a journal of the International Society for Gravitational Physiology vol. 9,1 (2002): P27-8.
Kirschnik U, Horn E, Agricola HJ. The influence of microgravity on the morphology of identified cerebral neurons in a cricket (Acheta domesticus). J Gravit Physiol. 2002 Jul;9(1):P27-8. PMID: 14703671.
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Hetero-Diels-Alder reactions of cyclic ketone derived enamide. A new and efficient concept for the asymmetric Robinson annulation.

Organic letters

Gallier F, Hussain H, Martel A, Kirschning A, Dujardin G.
PMID: 19537770
Org Lett. 2009 Jul 16;11(14):3060-3. doi: 10.1021/ol901065e.

Chiral enamides, easily prepared in one step from a cyclic ketone and an oxazolidinone, are successfully employed in high-yielding, endo, and facially selective Hetero-Diels-Alder reactions involving activated oxadienes and Siever's reagent as catalyst. From the resulting bicyclic heteroadducts, a...

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Gallier F, Hussain H, Martel A, et al. Hetero-Diels-Alder reactions of cyclic ketone derived enamide. A new and efficient concept for the asymmetric Robinson annulation. Org Lett. 2009;11(14):3060-3doi: 10.1021/ol901065e.
Gallier, F., Hussain, H., Martel, A., Kirschning, A., & Dujardin, G. (2009). Hetero-Diels-Alder reactions of cyclic ketone derived enamide. A new and efficient concept for the asymmetric Robinson annulation. Organic letters, 11(14), 3060-3. https://doi.org/10.1021/ol901065e
Gallier, Florian, et al. "Hetero-Diels-Alder reactions of cyclic ketone derived enamide. A new and efficient concept for the asymmetric Robinson annulation." Organic letters vol. 11,14 (2009): 3060-3. doi: https://doi.org/10.1021/ol901065e
Gallier F, Hussain H, Martel A, Kirschning A, Dujardin G. Hetero-Diels-Alder reactions of cyclic ketone derived enamide. A new and efficient concept for the asymmetric Robinson annulation. Org Lett. 2009 Jul 16;11(14):3060-3. doi: 10.1021/ol901065e. PMID: 19537770.
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Chemistry in flow systems II.

Beilstein journal of organic chemistry

Kirschning A.
PMID: 21915206
Beilstein J Org Chem. 2011;7:1046-7. doi: 10.3762/bjoc.7.119. Epub 2011 Aug 02.

No abstract available.

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Kirschning A. Chemistry in flow systems II. Beilstein J Org Chem. 2011;7:1046-7doi: 10.3762/bjoc.7.119.
Kirschning, A. (2011). Chemistry in flow systems II. Beilstein journal of organic chemistry, 71046-7. https://doi.org/10.3762/bjoc.7.119
Kirschning, Andreas. "Chemistry in flow systems II." Beilstein journal of organic chemistry vol. 7 (2011): 1046-7. doi: https://doi.org/10.3762/bjoc.7.119
Kirschning A. Chemistry in flow systems II. Beilstein J Org Chem. 2011;7:1046-7. doi: 10.3762/bjoc.7.119. Epub 2011 Aug 02. PMID: 21915206; PMCID: PMC3169419.
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Towards a biocompatible artificial lung: Covalent functionalization of poly(4-methylpent-1-ene) (TPX) with cRGD pentapeptide.

Beilstein journal of organic chemistry

Möller L, Hess C, Paleček J, Su Y, Haverich A, Kirschning A, Dräger G.
PMID: 23504394
Beilstein J Org Chem. 2013;9:270-7. doi: 10.3762/bjoc.9.33. Epub 2013 Feb 08.

Covalent multistep coating of poly(methylpentene), the membrane material in lung ventilators, by using a copper-free "click" approach with a modified cyclic RGD peptide, leads to a highly biocompatible poly(methylpentene) surface. The resulting modified membrane preserves the required excellent gas-flow...

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Möller L, Hess C, Paleček J, et al. Towards a biocompatible artificial lung: Covalent functionalization of poly(4-methylpent-1-ene) (TPX) with cRGD pentapeptide. Beilstein J Org Chem. 2013;9:270-7doi: 10.3762/bjoc.9.33.
Möller, L., Hess, C., Paleček, J., Su, Y., Haverich, A., Kirschning, A., & Dräger, G. (2013). Towards a biocompatible artificial lung: Covalent functionalization of poly(4-methylpent-1-ene) (TPX) with cRGD pentapeptide. Beilstein journal of organic chemistry, 9270-7. https://doi.org/10.3762/bjoc.9.33
Möller, Lena, et al. "Towards a biocompatible artificial lung: Covalent functionalization of poly(4-methylpent-1-ene) (TPX) with cRGD pentapeptide." Beilstein journal of organic chemistry vol. 9 (2013): 270-7. doi: https://doi.org/10.3762/bjoc.9.33
Möller L, Hess C, Paleček J, Su Y, Haverich A, Kirschning A, Dräger G. Towards a biocompatible artificial lung: Covalent functionalization of poly(4-methylpent-1-ene) (TPX) with cRGD pentapeptide. Beilstein J Org Chem. 2013;9:270-7. doi: 10.3762/bjoc.9.33. Epub 2013 Feb 08. PMID: 23504394; PMCID: PMC3596089.
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Chemistry in flow systems III.

Beilstein journal of organic chemistry

Kirschning A.
PMID: 24062829
Beilstein J Org Chem. 2013 Aug 16;9:1696-7. doi: 10.3762/bjoc.9.193. eCollection 2013.

No abstract available.

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Kirschning A. Chemistry in flow systems III. Beilstein J Org Chem. 2013;9:1696-7doi: 10.3762/bjoc.9.193.
Kirschning, A. (2013). Chemistry in flow systems III. Beilstein journal of organic chemistry, 91696-7. https://doi.org/10.3762/bjoc.9.193
Kirschning, Andreas. "Chemistry in flow systems III." Beilstein journal of organic chemistry vol. 9 (2013): 1696-7. doi: https://doi.org/10.3762/bjoc.9.193
Kirschning A. Chemistry in flow systems III. Beilstein J Org Chem. 2013 Aug 16;9:1696-7. doi: 10.3762/bjoc.9.193. eCollection 2013. PMID: 24062829; PMCID: PMC3778420.
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New Device for Ergonomic Control of a Surgical Robot with 4 DOF Including Haptic Feedback.

Biomedizinische Technik. Biomedical engineering

Neupert C, Klug F, Matich S, Kirschniak A, Pott PP, Schlaak HF, Werthschützky R.
PMID: 24043160
Biomed Tech (Berl). 2013 Aug;58. doi: 10.1515/bmt-2013-4404. Epub 2013 Sep 07.

No abstract available.

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Neupert C, Klug F, Matich S, et al. New Device for Ergonomic Control of a Surgical Robot with 4 DOF Including Haptic Feedback. Biomed Tech (Berl). 2013;58doi: 10.1515/bmt-2013-4404.
Neupert, C., Klug, F., Matich, S., Kirschniak, A., Pott, P. P., Schlaak, H. F., & Werthschützky, R. (2013). New Device for Ergonomic Control of a Surgical Robot with 4 DOF Including Haptic Feedback. Biomedizinische Technik. Biomedical engineering, 58. https://doi.org/10.1515/bmt-2013-4404
Neupert, Carsten, et al. "New Device for Ergonomic Control of a Surgical Robot with 4 DOF Including Haptic Feedback." Biomedizinische Technik. Biomedical engineering vol. 58 (2013). doi: https://doi.org/10.1515/bmt-2013-4404
Neupert C, Klug F, Matich S, Kirschniak A, Pott PP, Schlaak HF, Werthschützky R. New Device for Ergonomic Control of a Surgical Robot with 4 DOF Including Haptic Feedback. Biomed Tech (Berl). 2013 Aug;58. doi: 10.1515/bmt-2013-4404. Epub 2013 Sep 07. PMID: 24043160.
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Substrate specificity of α-humulene synthase from .

Engineering in life sciences

Alemdar S, König JC, Seidel K, Kirschning A, Scheper T, Beutel S.
PMID: 32624945
Eng Life Sci. 2018 Jul 03;18(9):654-658. doi: 10.1002/elsc.201800019. eCollection 2018 Sep.

Terpene synthases are the key enzymes in terpene biosynthesis that provide a structurally complex and highly diverse product spectrum. A suitable and reliable analytical assay is indispensable to measure terpene synthase activity accurately and precisely. In this study, a...

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Alemdar S, König JC, Seidel K, et al. Substrate specificity of α-humulene synthase from . Eng Life Sci. 2018;18(9):654-658doi: 10.1002/elsc.201800019.
Alemdar, S., König, J. C., Seidel, K., Kirschning, A., Scheper, T., & Beutel, S. (2018). Substrate specificity of α-humulene synthase from . Engineering in life sciences, 18(9), 654-658. https://doi.org/10.1002/elsc.201800019
Alemdar, Semra, et al. "Substrate specificity of α-humulene synthase from ." Engineering in life sciences vol. 18,9 (2018): 654-658. doi: https://doi.org/10.1002/elsc.201800019
Alemdar S, König JC, Seidel K, Kirschning A, Scheper T, Beutel S. Substrate specificity of α-humulene synthase from . Eng Life Sci. 2018 Jul 03;18(9):654-658. doi: 10.1002/elsc.201800019. eCollection 2018 Sep. PMID: 32624945; PMCID: PMC6999270.
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Author Correction: Insights into a dual function amide oxidase/macrocyclase from lankacidin biosynthesis.

Nature communications

Dorival J, Risser F, Jacob C, Collin S, Dräger G, Paris C, Chagot B, Kirschning A, Gruez A, Weissman KJ.
PMID: 31996686
Nat Commun. 2020 Jan 29;11(1):683. doi: 10.1038/s41467-020-14473-z.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

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Dorival J, Risser F, Jacob C, et al. Author Correction: Insights into a dual function amide oxidase/macrocyclase from lankacidin biosynthesis. Nat Commun. 2020;11(1):683doi: 10.1038/s41467-020-14473-z.
Dorival, J., Risser, F., Jacob, C., Collin, S., Dräger, G., Paris, C., Chagot, B., Kirschning, A., Gruez, A., & Weissman, K. J. (2020). Author Correction: Insights into a dual function amide oxidase/macrocyclase from lankacidin biosynthesis. Nature communications, 11(1), 683. https://doi.org/10.1038/s41467-020-14473-z
Dorival, Jonathan, et al. "Author Correction: Insights into a dual function amide oxidase/macrocyclase from lankacidin biosynthesis." Nature communications vol. 11,1 (2020): 683. doi: https://doi.org/10.1038/s41467-020-14473-z
Dorival J, Risser F, Jacob C, Collin S, Dräger G, Paris C, Chagot B, Kirschning A, Gruez A, Weissman KJ. Author Correction: Insights into a dual function amide oxidase/macrocyclase from lankacidin biosynthesis. Nat Commun. 2020 Jan 29;11(1):683. doi: 10.1038/s41467-020-14473-z. PMID: 31996686; PMCID: PMC6989693.
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Novel box trainer for taTME - prospective evaluation among medical students.

Innovative surgical sciences

Mann J, Rolinger J, Axt S, Kirschniak A, Wilhelm P.
PMID: 31709303
Innov Surg Sci. 2019 Oct 07;4(3):116-120. doi: 10.1515/iss-2019-0013. eCollection 2019 Sep.

BACKGROUND: Transanal total mesorectal excision (taTME) has been subject to extensive research and increasing clinical application. It allows further reduction of trauma by accessing via a natural orifice. Manifold platforms and instruments have been introduced and heterogeneity in surgical...

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Mann J, Rolinger J, Axt S, et al. Novel box trainer for taTME - prospective evaluation among medical students. Innov Surg Sci. 2019;4(3):116-120doi: 10.1515/iss-2019-0013.
Mann, J., Rolinger, J., Axt, S., Kirschniak, A., & Wilhelm, P. (2019). Novel box trainer for taTME - prospective evaluation among medical students. Innovative surgical sciences, 4(3), 116-120. https://doi.org/10.1515/iss-2019-0013
Mann, Jakob, et al. "Novel box trainer for taTME - prospective evaluation among medical students." Innovative surgical sciences vol. 4,3 (2019): 116-120. doi: https://doi.org/10.1515/iss-2019-0013
Mann J, Rolinger J, Axt S, Kirschniak A, Wilhelm P. Novel box trainer for taTME - prospective evaluation among medical students. Innov Surg Sci. 2019 Oct 07;4(3):116-120. doi: 10.1515/iss-2019-0013. eCollection 2019 Sep. PMID: 31709303; PMCID: PMC6817727.
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Long-term results of the custom- made hip endoprostheses Evolution K® and Adaptiva®: A prospective cohort study.

Orthopedic reviews

Axt S, Kirschniak A, Axt L, Braun M, Beltzer C, Leichtle C, Leichtle U.
PMID: 33907614
Orthop Rev (Pavia). 2021 Apr 07;13(1):9014. doi: 10.4081/or.2021.9014. eCollection 2021 Mar 30.

The aim of our study is to evaluate clinical long-term results and determine changes in periprosthetic bone density of the custom-made hip prostheses Evolution-K

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Axt S, Kirschniak A, Axt L, et al. Long-term results of the custom- made hip endoprostheses Evolution K® and Adaptiva®: A prospective cohort study. Orthop Rev (Pavia). 2021;13(1):9014doi: 10.4081/or.2021.9014.
Axt, S., Kirschniak, A., Axt, L., Braun, M., Beltzer, C., Leichtle, C., & Leichtle, U. (2021). Long-term results of the custom- made hip endoprostheses Evolution K® and Adaptiva®: A prospective cohort study. Orthopedic reviews, 13(1), 9014. https://doi.org/10.4081/or.2021.9014
Axt, Steffen, et al. "Long-term results of the custom- made hip endoprostheses Evolution K® and Adaptiva®: A prospective cohort study." Orthopedic reviews vol. 13,1 (2021): 9014. doi: https://doi.org/10.4081/or.2021.9014
Axt S, Kirschniak A, Axt L, Braun M, Beltzer C, Leichtle C, Leichtle U. Long-term results of the custom- made hip endoprostheses Evolution K® and Adaptiva®: A prospective cohort study. Orthop Rev (Pavia). 2021 Apr 07;13(1):9014. doi: 10.4081/or.2021.9014. eCollection 2021 Mar 30. PMID: 33907614; PMCID: PMC8056321.
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Showing 1 to 12 of 65 entries