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On the synthesis of quinoline alkaloids in plants. 2. Fermentativ conversion of the penicillin alkaloids cyclopenin and cyclopenol to viridicatin and …

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[No authors listed]
GSID: 7YZTyqKuCdoJ
M Luckner - European journal of biochemistry, 1967 - pubmed.ncbi.nlm.nih.gov

[On the synthesis of quinoline alkaloids in plants. 2. Fermentativ conversion of the penicillin alkaloids cyclopenin and cyclopenol to viridicatin and viridicatol] [On the synthesis of …

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Luckner, M. (1967). On the synthesis of quinoline alkaloids in plants. 2. Fermentativ conversion of the penicillin alkaloids cyclopenin and cyclopenol to viridicatin and viridicatol. European journal of biochemistry, 2(1), 74-78.
Luckner, M. "On the synthesis of quinoline alkaloids in plants. 2. Fermentativ conversion of the penicillin alkaloids cyclopenin and cyclopenol to viridicatin and viridicatol." European journal of biochemistry 2.1 (1967): 74-78.
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Synthesis, structure and spectral properties of O,N,N coordinating ligands and their neutral Zn(ii) complexes: a combined experimental and theoretical study.

Dalton transactions (Cambridge, England : 2003)

Hens A, Mondal P, Rajak KK.
PMID: 23995072
Dalton Trans. 2013 Oct 01;42(41):14905-15. doi: 10.1039/c3dt51571k.

Mononuclear Zn(ii) complexes with the general formula [Zn(L)2] have been synthesized in good yields by reacting Zn(OAc)2 with HL in a ratio of 1 : 2 in methanol solvent. Here L is the deprotonated form of 6-[(quinolin-8-ylamino)methylene]cyclohexa-2,4-dienone (HL(1)), 4-chloro-6-[(quinolin-8-ylamino)methylene]cyclohexa-2,4-dienone...

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Hens A, Mondal P, Rajak KK. Synthesis, structure and spectral properties of O,N,N coordinating ligands and their neutral Zn(ii) complexes: a combined experimental and theoretical study. Dalton Trans. 2013;42(41):14905-15doi: 10.1039/c3dt51571k.
Hens, A., Mondal, P., & Rajak, K. K. (2013). Synthesis, structure and spectral properties of O,N,N coordinating ligands and their neutral Zn(ii) complexes: a combined experimental and theoretical study. Dalton transactions (Cambridge, England : 2003), 42(41), 14905-15. https://doi.org/10.1039/c3dt51571k
Hens, Amar, et al. "Synthesis, structure and spectral properties of O,N,N coordinating ligands and their neutral Zn(ii) complexes: a combined experimental and theoretical study." Dalton transactions (Cambridge, England : 2003) vol. 42,41 (2013): 14905-15. doi: https://doi.org/10.1039/c3dt51571k
Hens A, Mondal P, Rajak KK. Synthesis, structure and spectral properties of O,N,N coordinating ligands and their neutral Zn(ii) complexes: a combined experimental and theoretical study. Dalton Trans. 2013 Oct 01;42(41):14905-15. doi: 10.1039/c3dt51571k. PMID: 23995072.
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Preparation of RHgCl via transmetalation of (8-quinolyl)SnMe₃ and redistribution to R₂Hg (R = 8-quinolyl): a highly distorted diorganomercury(II) with 84 degree C-Hg-C angle.

Dalton transactions (Cambridge, England : 2003)

Tamang SR, Son JH, Hoefelmeyer JD.
PMID: 24671445
Dalton Trans. 2014 May 21;43(19):7139-45. doi: 10.1039/c4dt00384e. Epub 2014 Mar 27.

Transmetalation occurs upon addition of HgCl2 to (8-quinolyl)SnMe3 to yield (8-quinolyl)HgCl. The molecule features a frustrated Hg-N Lewis pair; however the mercury(II) center showed low affinity for sulfur Lewis bases, S8 or thiophene. In the presence of NH4SCN, ligand...

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Tamang SR, Son JH, Hoefelmeyer JD. Preparation of RHgCl via transmetalation of (8-quinolyl)SnMe₃ and redistribution to R₂Hg (R = 8-quinolyl): a highly distorted diorganomercury(II) with 84 degree C-Hg-C angle. Dalton Trans. 2014;43(19):7139-45doi: 10.1039/c4dt00384e.
Tamang, S. R., Son, J. H., & Hoefelmeyer, J. D. (2014). Preparation of RHgCl via transmetalation of (8-quinolyl)SnMe₃ and redistribution to R₂Hg (R = 8-quinolyl): a highly distorted diorganomercury(II) with 84 degree C-Hg-C angle. Dalton transactions (Cambridge, England : 2003), 43(19), 7139-45. https://doi.org/10.1039/c4dt00384e
Tamang, Sem Raj, et al. "Preparation of RHgCl via transmetalation of (8-quinolyl)SnMe₃ and redistribution to R₂Hg (R = 8-quinolyl): a highly distorted diorganomercury(II) with 84 degree C-Hg-C angle." Dalton transactions (Cambridge, England : 2003) vol. 43,19 (2014): 7139-45. doi: https://doi.org/10.1039/c4dt00384e
Tamang SR, Son JH, Hoefelmeyer JD. Preparation of RHgCl via transmetalation of (8-quinolyl)SnMe₃ and redistribution to R₂Hg (R = 8-quinolyl): a highly distorted diorganomercury(II) with 84 degree C-Hg-C angle. Dalton Trans. 2014 May 21;43(19):7139-45. doi: 10.1039/c4dt00384e. Epub 2014 Mar 27. PMID: 24671445.
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Pure red phosphorescent organic light-emitting diodes made of iridium(III) complex with thiophene-quinoline ligand.

Journal of nanoscience and nanotechnology

Lim JM, Kwon JY, Xu F, Kim HU, Hwang DH.
PMID: 24266181
J Nanosci Nanotechnol. 2013 Dec;13(12):8007-10. doi: 10.1166/jnn.2013.8152.

A cyclometalated iridium(II) complex, bis(2-thiophen-2-yl-quinolinato)(acetoacetonate)iridium(II) [(tq)2Ir(III)(acac)] was synthesized for use in phosphorescent organic light-emitting diodes. The photophysical and electrochemical properties of the iridium(Ill) complex were characterized by UV-visible absorption, photoluminescence, and cyclic voltammetry. The maximum UV-visible absorption of (tq)2Ir(acac)...

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Lim JM, Kwon JY, Xu F, et al. Pure red phosphorescent organic light-emitting diodes made of iridium(III) complex with thiophene-quinoline ligand. J Nanosci Nanotechnol. 2013;13(12):8007-10doi: 10.1166/jnn.2013.8152.
Lim, J. M., Kwon, J. Y., Xu, F., Kim, H. U., & Hwang, D. H. (2013). Pure red phosphorescent organic light-emitting diodes made of iridium(III) complex with thiophene-quinoline ligand. Journal of nanoscience and nanotechnology, 13(12), 8007-10. https://doi.org/10.1166/jnn.2013.8152
Lim, Jong Min, et al. "Pure red phosphorescent organic light-emitting diodes made of iridium(III) complex with thiophene-quinoline ligand." Journal of nanoscience and nanotechnology vol. 13,12 (2013): 8007-10. doi: https://doi.org/10.1166/jnn.2013.8152
Lim JM, Kwon JY, Xu F, Kim HU, Hwang DH. Pure red phosphorescent organic light-emitting diodes made of iridium(III) complex with thiophene-quinoline ligand. J Nanosci Nanotechnol. 2013 Dec;13(12):8007-10. doi: 10.1166/jnn.2013.8152. PMID: 24266181.
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Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization.

Chemical record (New York, N.Y.)

Chelucci G, Porcheddu A.
PMID: 27524555
Chem Rec. 2017 Feb;17(2):200-216. doi: 10.1002/tcr.201600083. Epub 2016 Aug 15.

Efficient ruthenium-, rhodium-, palladium-, copper- and iridium-catalysed methodologies have been recently developed for the synthesis of quinolines by the reaction of 2-aminobenzyl alcohols with carbonyl compounds (aldehydes and ketones) or the related alcohols. The reaction is assumed to proceed...

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Chelucci G, Porcheddu A. Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chem Rec. 2016;17(2):200-216doi: 10.1002/tcr.201600083.
Chelucci, G., & Porcheddu, A. (2017). Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chemical record (New York, N.Y.), 17(2), 200-216. https://doi.org/10.1002/tcr.201600083
Chelucci, Giorgio, and Porcheddu, Andrea. "Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization." Chemical record (New York, N.Y.) vol. 17,2 (2017): 200-216. doi: https://doi.org/10.1002/tcr.201600083
Chelucci G, Porcheddu A. Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chem Rec. 2017 Feb;17(2):200-216. doi: 10.1002/tcr.201600083. Epub 2016 Aug 15. PMID: 27524555.
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Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies.

Journal of fluorescence

Shabir G, Saeed A, Arshad M, Zahid M.
PMID: 27672080
J Fluoresc. 2016 Nov;26(6):2247-2255. doi: 10.1007/s10895-016-1920-2. Epub 2016 Sep 27.

In the present paper a novel way of symmetric conjugation extension along molecular axes of perylene dianhydride chromophore has been devised to achieve lengthy delocalized electronic species exhibiting red shifted absorption and emission of UV-Visible radiations. During synthetic pathway...

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Shabir G, Saeed A, Arshad M, et al. Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies. J Fluoresc. 2016;26(6):2247-2255doi: 10.1007/s10895-016-1920-2.
Shabir, G., Saeed, A., Arshad, M., & Zahid, M. (2016). Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies. Journal of fluorescence, 26(6), 2247-2255. https://doi.org/10.1007/s10895-016-1920-2
Shabir, Ghulam, et al. "Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies." Journal of fluorescence vol. 26,6 (2016): 2247-2255. doi: https://doi.org/10.1007/s10895-016-1920-2
Shabir G, Saeed A, Arshad M, Zahid M. Multichromic Bis-Axially Extended Perylene Chromophore with Schiff Bases: Synthesis, Characterization and Electrochemical Studies. J Fluoresc. 2016 Nov;26(6):2247-2255. doi: 10.1007/s10895-016-1920-2. Epub 2016 Sep 27. PMID: 27672080.
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Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N-H and Aryl C-H Bond Cleavage.

Angewandte Chemie (International ed. in English)

Zhang W, Chen P, Liu G.
PMID: 28387449
Angew Chem Int Ed Engl. 2017 May 02;56(19):5336-5340. doi: 10.1002/anie.201700889. Epub 2017 Apr 07.

An asymmetric palladium-catalyzed intramolecular oxidative aminoarylation of alkenes has been developed with quinoline-oxazoline chiral ligands and Ag

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Zhang W, Chen P, Liu G. Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N-H and Aryl C-H Bond Cleavage. Angew Chem Int Ed Engl. 2017;56(19):5336-5340doi: 10.1002/anie.201700889.
Zhang, W., Chen, P., & Liu, G. (2017). Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N-H and Aryl C-H Bond Cleavage. Angewandte Chemie (International ed. in English), 56(19), 5336-5340. https://doi.org/10.1002/anie.201700889
Zhang, Wen, et al. "Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N-H and Aryl C-H Bond Cleavage." Angewandte Chemie (International ed. in English) vol. 56,19 (2017): 5336-5340. doi: https://doi.org/10.1002/anie.201700889
Zhang W, Chen P, Liu G. Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N-H and Aryl C-H Bond Cleavage. Angew Chem Int Ed Engl. 2017 May 02;56(19):5336-5340. doi: 10.1002/anie.201700889. Epub 2017 Apr 07. PMID: 28387449.
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Oxidative Radical Addition/Cyclization Cascade for the Construction of Carbonyl-Containing Quinoline-2,4(1H,3H)-Diones.

The Journal of organic chemistry

Wang SS, Fu H, Shen Y, Sun M, Li YM.
PMID: 26938786
J Org Chem. 2016 Apr 01;81(7):2920-9. doi: 10.1021/acs.joc.6b00210. Epub 2016 Mar 11.

Oxidative radical addition/cyclization cascade of o-cyanoarylacrylamides with α-keto acids as well as aldehydes is reported. This transformation exhibits a wide substrate scope and significant functional group tolerance and provides a convenient and highly efficient access to carbonyl-containing quinoline-2,4(1H,3H)-diones. A...

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Wang SS, Fu H, Shen Y, et al. Oxidative Radical Addition/Cyclization Cascade for the Construction of Carbonyl-Containing Quinoline-2,4(1H,3H)-Diones. J Org Chem. 2016;81(7):2920-9doi: 10.1021/acs.joc.6b00210.
Wang, S. S., Fu, H., Shen, Y., Sun, M., & Li, Y. M. (2016). Oxidative Radical Addition/Cyclization Cascade for the Construction of Carbonyl-Containing Quinoline-2,4(1H,3H)-Diones. The Journal of organic chemistry, 81(7), 2920-9. https://doi.org/10.1021/acs.joc.6b00210
Wang, Shi-Sheng, et al. "Oxidative Radical Addition/Cyclization Cascade for the Construction of Carbonyl-Containing Quinoline-2,4(1H,3H)-Diones." The Journal of organic chemistry vol. 81,7 (2016): 2920-9. doi: https://doi.org/10.1021/acs.joc.6b00210
Wang SS, Fu H, Shen Y, Sun M, Li YM. Oxidative Radical Addition/Cyclization Cascade for the Construction of Carbonyl-Containing Quinoline-2,4(1H,3H)-Diones. J Org Chem. 2016 Apr 01;81(7):2920-9. doi: 10.1021/acs.joc.6b00210. Epub 2016 Mar 11. PMID: 26938786.
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Traceless Directing-Group Strategy in the Ru-Catalyzed, Formal [3 + 3] Annulation of Anilines with Allyl Alcohols: A One-Pot, Domino Approach for the Synthesis of Quinolines.

Organic letters

Kumar GS, Kumar P, Kapur M.
PMID: 28448156
Org Lett. 2017 May 19;19(10):2494-2497. doi: 10.1021/acs.orglett.7b00715. Epub 2017 Apr 27.

A unique, ruthenium-catalyzed, [3 + 3] annulation of anilines with allyl alcohols in the synthesis of substituted quinolines is reported. The method employs a traceless directing group strategy in the proximal C-H bond activation and represents a one-pot Domino...

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Kumar GS, Kumar P, Kapur M. Traceless Directing-Group Strategy in the Ru-Catalyzed, Formal [3 + 3] Annulation of Anilines with Allyl Alcohols: A One-Pot, Domino Approach for the Synthesis of Quinolines. Org Lett. 2017;19(10):2494-2497doi: 10.1021/acs.orglett.7b00715.
Kumar, G. S., Kumar, P., & Kapur, M. (2017). Traceless Directing-Group Strategy in the Ru-Catalyzed, Formal [3 + 3] Annulation of Anilines with Allyl Alcohols: A One-Pot, Domino Approach for the Synthesis of Quinolines. Organic letters, 19(10), 2494-2497. https://doi.org/10.1021/acs.orglett.7b00715
Kumar, Gangam Srikanth, et al. "Traceless Directing-Group Strategy in the Ru-Catalyzed, Formal [3 + 3] Annulation of Anilines with Allyl Alcohols: A One-Pot, Domino Approach for the Synthesis of Quinolines." Organic letters vol. 19,10 (2017): 2494-2497. doi: https://doi.org/10.1021/acs.orglett.7b00715
Kumar GS, Kumar P, Kapur M. Traceless Directing-Group Strategy in the Ru-Catalyzed, Formal [3 + 3] Annulation of Anilines with Allyl Alcohols: A One-Pot, Domino Approach for the Synthesis of Quinolines. Org Lett. 2017 May 19;19(10):2494-2497. doi: 10.1021/acs.orglett.7b00715. Epub 2017 Apr 27. PMID: 28448156.
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Crystal structure of hexa-aqua-nickel(II) bis{2-[(5,6-di-hy-droxy-3-sul-fon-ato-quino-lin-1-ium-7-yl)oxy]acetate} dihydrate.

Acta crystallographica. Section E, Crystallographic communications

Le Thi Hong H, Nguyen Thi Ngoc V, Tran Thi D, Nguyen Bich N, Van Meervelt L.
PMID: 26396859
Acta Crystallogr E Crystallogr Commun. 2015 Aug 26;71:1105-8. doi: 10.1107/S2056989015015662. eCollection 2015 Sep 01.

The asymmetric unit of the title compound, [Ni(H2O)6](C11H8NO8S)2·2H2O, features a half-hexa-aqua-nickel(II) complex cation with the Ni(II) ion on an inversion center, one deprotonated 5,6-dihy-droxy-3-sulfoquinolin-7-yloxyacetic acid (QOH) molecule appearing in its zwitterionic form and one lattice water mol-ecule. The sulfonate...

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Le Thi Hong H, Nguyen Thi Ngoc V, Tran Thi D, et al. Crystal structure of hexa-aqua-nickel(II) bis{2-[(5,6-di-hy-droxy-3-sul-fon-ato-quino-lin-1-ium-7-yl)oxy]acetate} dihydrate. Acta Crystallogr E Crystallogr Commun. 2015;71:1105-8doi: 10.1107/S2056989015015662.
Le Thi Hong, H., Nguyen Thi Ngoc, V., Tran Thi, D., Nguyen Bich, N., & Van Meervelt, L. (2015). Crystal structure of hexa-aqua-nickel(II) bis{2-[(5,6-di-hy-droxy-3-sul-fon-ato-quino-lin-1-ium-7-yl)oxy]acetate} dihydrate. Acta crystallographica. Section E, Crystallographic communications, 711105-8. https://doi.org/10.1107/S2056989015015662
Le Thi Hong, Hai, et al. "Crystal structure of hexa-aqua-nickel(II) bis{2-[(5,6-di-hy-droxy-3-sul-fon-ato-quino-lin-1-ium-7-yl)oxy]acetate} dihydrate." Acta crystallographica. Section E, Crystallographic communications vol. 71 (2015): 1105-8. doi: https://doi.org/10.1107/S2056989015015662
Le Thi Hong H, Nguyen Thi Ngoc V, Tran Thi D, Nguyen Bich N, Van Meervelt L. Crystal structure of hexa-aqua-nickel(II) bis{2-[(5,6-di-hy-droxy-3-sul-fon-ato-quino-lin-1-ium-7-yl)oxy]acetate} dihydrate. Acta Crystallogr E Crystallogr Commun. 2015 Aug 26;71:1105-8. doi: 10.1107/S2056989015015662. eCollection 2015 Sep 01. PMID: 26396859; PMCID: PMC4555394.
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Insight into the effects of modifying chromophores on the performance of quinoline-based dye-sensitized solar cells.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Mao M, Wang JB, Liu XL, Wu GH, Fang XQ, Song QH.
PMID: 28892718
Spectrochim Acta A Mol Biomol Spectrosc. 2018 Feb 05;190:23-32. doi: 10.1016/j.saa.2017.09.002. Epub 2017 Sep 04.

A series of organic dyes based on quinoline as an electron-deficient π-linker, were designed and synthesized for dye sensitized solar cells (DSSC) application. These push-pull conjugated dyes, sharing same anchoring group with distinctive electron-rich donating groups such as N,N-diethyl...

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Mao M, Wang JB, Liu XL, et al. Insight into the effects of modifying chromophores on the performance of quinoline-based dye-sensitized solar cells. Spectrochim Acta A Mol Biomol Spectrosc. 2017;190:23-32doi: 10.1016/j.saa.2017.09.002.
Mao, M., Wang, J. B., Liu, X. L., Wu, G. H., Fang, X. Q., & Song, Q. H. (2018). Insight into the effects of modifying chromophores on the performance of quinoline-based dye-sensitized solar cells. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 19023-32. https://doi.org/10.1016/j.saa.2017.09.002
Mao, Mao, et al. "Insight into the effects of modifying chromophores on the performance of quinoline-based dye-sensitized solar cells." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 190 (2018): 23-32. doi: https://doi.org/10.1016/j.saa.2017.09.002
Mao M, Wang JB, Liu XL, Wu GH, Fang XQ, Song QH. Insight into the effects of modifying chromophores on the performance of quinoline-based dye-sensitized solar cells. Spectrochim Acta A Mol Biomol Spectrosc. 2018 Feb 05;190:23-32. doi: 10.1016/j.saa.2017.09.002. Epub 2017 Sep 04. PMID: 28892718.
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Influence of Donor on the Sensing Performance of a Series of Through-Bond Energy Transfer-Based Two-photon Fluorescent Cu(2+) Probes.

Photochemistry and photobiology

Zhang YJ, Wang X, Zhou Y, Wang CK.
PMID: 27144496
Photochem Photobiol. 2016 Jul;92(4):528-36. doi: 10.1111/php.12597. Epub 2016 Jun 29.

Optical properties of a series of molecular two-photon fluorescent Cu(2+) probes containing the same acceptor (rhodamine group) are analyzed using time-dependent density functional theory in combination with analytical response theory. Special emphasis is placed on evolution of the probes'...

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Zhang YJ, Wang X, Zhou Y, et al. Influence of Donor on the Sensing Performance of a Series of Through-Bond Energy Transfer-Based Two-photon Fluorescent Cu(2+) Probes. Photochem Photobiol. 2016;92(4):528-36doi: 10.1111/php.12597.
Zhang, Y. J., Wang, X., Zhou, Y., & Wang, C. K. (2016). Influence of Donor on the Sensing Performance of a Series of Through-Bond Energy Transfer-Based Two-photon Fluorescent Cu(2+) Probes. Photochemistry and photobiology, 92(4), 528-36. https://doi.org/10.1111/php.12597
Zhang, Yu-Jin, et al. "Influence of Donor on the Sensing Performance of a Series of Through-Bond Energy Transfer-Based Two-photon Fluorescent Cu(2+) Probes." Photochemistry and photobiology vol. 92,4 (2016): 528-36. doi: https://doi.org/10.1111/php.12597
Zhang YJ, Wang X, Zhou Y, Wang CK. Influence of Donor on the Sensing Performance of a Series of Through-Bond Energy Transfer-Based Two-photon Fluorescent Cu(2+) Probes. Photochem Photobiol. 2016 Jul;92(4):528-36. doi: 10.1111/php.12597. Epub 2016 Jun 29. PMID: 27144496.
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