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Showing 13 to 18 of 18 entries
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A General Synthetic Route to Isomeric Pyrrolo[1,2- x][1,4]diazepinones.

The Journal of organic chemistry

Zelina EY, Nevolina TA, Sorotskaja LN, Skvortsov DA, Trushkov IV, Uchuskin MG.
PMID: 30148633
J Org Chem. 2018 Oct 05;83(19):11747-11757. doi: 10.1021/acs.joc.8b01669. Epub 2018 Sep 05.

A simple one-pot method for the synthesis of isomeric pyrrolo[1,2- x][1,4]diazepinones in reasonable yields was developed. The method is based on the condensation of readily available N-Boc amino acids with biomass-derived furans containing aminoalkyl groups followed by deprotection, furan...

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Zelina EY, Nevolina TA, Sorotskaja LN, et al. A General Synthetic Route to Isomeric Pyrrolo[1,2- x][1,4]diazepinones. J Org Chem. 2018;83(19):11747-11757doi: 10.1021/acs.joc.8b01669.
Zelina, E. Y., Nevolina, T. A., Sorotskaja, L. N., Skvortsov, D. A., Trushkov, I. V., & Uchuskin, M. G. (2018). A General Synthetic Route to Isomeric Pyrrolo[1,2- x][1,4]diazepinones. The Journal of organic chemistry, 83(19), 11747-11757. https://doi.org/10.1021/acs.joc.8b01669
Zelina, Elena Y, et al. "A General Synthetic Route to Isomeric Pyrrolo[1,2- x][1,4]diazepinones." The Journal of organic chemistry vol. 83,19 (2018): 11747-11757. doi: https://doi.org/10.1021/acs.joc.8b01669
Zelina EY, Nevolina TA, Sorotskaja LN, Skvortsov DA, Trushkov IV, Uchuskin MG. A General Synthetic Route to Isomeric Pyrrolo[1,2- x][1,4]diazepinones. J Org Chem. 2018 Oct 05;83(19):11747-11757. doi: 10.1021/acs.joc.8b01669. Epub 2018 Sep 05. PMID: 30148633.
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Roaming-Mediated CH.

ChemistryOpen

Zhang M, Guo H, Zhang L.
PMID: 28168149
ChemistryOpen. 2017 Jan 18;6(1):40-45. doi: 10.1002/open.201600144. eCollection 2017 Feb.

The ionization of aromatic ethylamines by photons or electrons leads to elimination of CH

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Zhang M, Guo H, Zhang L. Roaming-Mediated CH. ChemistryOpen. 2017;6(1):40-45doi: 10.1002/open.201600144.
Zhang, M., Guo, H., & Zhang, L. (2017). Roaming-Mediated CH. ChemistryOpen, 6(1), 40-45. https://doi.org/10.1002/open.201600144
Zhang, Mengxing, et al. "Roaming-Mediated CH." ChemistryOpen vol. 6,1 (2017): 40-45. doi: https://doi.org/10.1002/open.201600144
Zhang M, Guo H, Zhang L. Roaming-Mediated CH. ChemistryOpen. 2017 Jan 18;6(1):40-45. doi: 10.1002/open.201600144. eCollection 2017 Feb. PMID: 28168149; PMCID: PMC5288767.
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Reconsideration of the Zincke salt: An efficient colorimetric chemosensor for detection of ethylamines.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Kim JH.
PMID: 29179088
Spectrochim Acta A Mol Biomol Spectrosc. 2018 Mar 05;192:378-383. doi: 10.1016/j.saa.2017.11.039. Epub 2017 Nov 21.

In this work, an efficient colorimetric chemosensor for the detection of ethylamines using a pyridinium salt (the Zincke salt) is reported. Highly sensitive and selective reactivity of the Zincke salt enables colorimetric response of the Zincke salt solution to...

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Kim JH. Reconsideration of the Zincke salt: An efficient colorimetric chemosensor for detection of ethylamines. Spectrochim Acta A Mol Biomol Spectrosc. 2017;192:378-383doi: 10.1016/j.saa.2017.11.039.
Kim, J. H. (2018). Reconsideration of the Zincke salt: An efficient colorimetric chemosensor for detection of ethylamines. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 192378-383. https://doi.org/10.1016/j.saa.2017.11.039
Kim, Jong H. "Reconsideration of the Zincke salt: An efficient colorimetric chemosensor for detection of ethylamines." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 192 (2018): 378-383. doi: https://doi.org/10.1016/j.saa.2017.11.039
Kim JH. Reconsideration of the Zincke salt: An efficient colorimetric chemosensor for detection of ethylamines. Spectrochim Acta A Mol Biomol Spectrosc. 2018 Mar 05;192:378-383. doi: 10.1016/j.saa.2017.11.039. Epub 2017 Nov 21. PMID: 29179088.
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Brønsted Acid Mediated Cascade Reaction To Access 3-(2-Bromoethyl)benzofurans.

Organic letters

Porcu S, Demuro S, Luridiana A, Cocco A, Frongia A, Aitken DJ, Charnay-Pouget F, Guillot R, Sarais G, Secci F.
PMID: 30422665
Org Lett. 2018 Dec 07;20(23):7699-7702. doi: 10.1021/acs.orglett.8b03429. Epub 2018 Nov 13.

A unified protocol for the construction of 3-(2-bromoethyl)benzofurans and 2-(benzofuran-3-yl)ethylamines from bis[(trimethylsilyl)oxy]cyclobutene has been developed. This mild and facile strategy was applied for the synthesis of a series of 5-HT serotonin receptor agonists, underlining its potential for the syntheses...

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Porcu S, Demuro S, Luridiana A, et al. Brønsted Acid Mediated Cascade Reaction To Access 3-(2-Bromoethyl)benzofurans. Org Lett. 2018;20(23):7699-7702doi: 10.1021/acs.orglett.8b03429.
Porcu, S., Demuro, S., Luridiana, A., Cocco, A., Frongia, A., Aitken, D. J., Charnay-Pouget, F., Guillot, R., Sarais, G., & Secci, F. (2018). Brønsted Acid Mediated Cascade Reaction To Access 3-(2-Bromoethyl)benzofurans. Organic letters, 20(23), 7699-7702. https://doi.org/10.1021/acs.orglett.8b03429
Porcu, Stefania, et al. "Brønsted Acid Mediated Cascade Reaction To Access 3-(2-Bromoethyl)benzofurans." Organic letters vol. 20,23 (2018): 7699-7702. doi: https://doi.org/10.1021/acs.orglett.8b03429
Porcu S, Demuro S, Luridiana A, Cocco A, Frongia A, Aitken DJ, Charnay-Pouget F, Guillot R, Sarais G, Secci F. Brønsted Acid Mediated Cascade Reaction To Access 3-(2-Bromoethyl)benzofurans. Org Lett. 2018 Dec 07;20(23):7699-7702. doi: 10.1021/acs.orglett.8b03429. Epub 2018 Nov 13. PMID: 30422665.
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Merging Photoredox/Nickel Catalysis for Cross-Electrophile Coupling of Aziridines with Pyridin-1-ium Salts via Dearomatization.

Organic letters

Xu CH, Li JH, Xiang JN, Deng W.
PMID: 33825468
Org Lett. 2021 May 07;23(9):3696-3700. doi: 10.1021/acs.orglett.1c01077. Epub 2021 Apr 07.

Merging photoredox/nickel catalysis enabling the cross-electrophile coupling of aziridines with pyridin-1-ium salts involving dearomatization for the synthesis of β-(1,4-dihydropyridin-4-yl)-ethylamines, especially including bioactive motif-based analogues, is described. This method allows incorporation of a 1,4-dihydropyridin-4-yl group and formation a N-H amino...

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Xu CH, Li JH, Xiang JN, et al. Merging Photoredox/Nickel Catalysis for Cross-Electrophile Coupling of Aziridines with Pyridin-1-ium Salts via Dearomatization. Org Lett. 2021;23(9):3696-3700doi: 10.1021/acs.orglett.1c01077.
Xu, C. H., Li, J. H., Xiang, J. N., & Deng, W. (2021). Merging Photoredox/Nickel Catalysis for Cross-Electrophile Coupling of Aziridines with Pyridin-1-ium Salts via Dearomatization. Organic letters, 23(9), 3696-3700. https://doi.org/10.1021/acs.orglett.1c01077
Xu, Chong-Hui, et al. "Merging Photoredox/Nickel Catalysis for Cross-Electrophile Coupling of Aziridines with Pyridin-1-ium Salts via Dearomatization." Organic letters vol. 23,9 (2021): 3696-3700. doi: https://doi.org/10.1021/acs.orglett.1c01077
Xu CH, Li JH, Xiang JN, Deng W. Merging Photoredox/Nickel Catalysis for Cross-Electrophile Coupling of Aziridines with Pyridin-1-ium Salts via Dearomatization. Org Lett. 2021 May 07;23(9):3696-3700. doi: 10.1021/acs.orglett.1c01077. Epub 2021 Apr 07. PMID: 33825468.
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Enzymatic Preparation of Aromatic Ethylamines from Aromatic L-Amino Acids.

Bioscience, biotechnology, and biochemistry

Nakazawa H, Sano K, Matsuda K, Mitsugi K.
PMID: 27281009
Biosci Biotechnol Biochem. 1993 Jan;57(7):1210-1. doi: 10.1271/bbb.57.1210.

No abstract available.

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Nakazawa H, Sano K, Matsuda K, et al. Enzymatic Preparation of Aromatic Ethylamines from Aromatic L-Amino Acids. Biosci Biotechnol Biochem. 1993;57(7):1210-1doi: 10.1271/bbb.57.1210.
Nakazawa, H., Sano, K., Matsuda, K., & Mitsugi, K. (1993). Enzymatic Preparation of Aromatic Ethylamines from Aromatic L-Amino Acids. Bioscience, biotechnology, and biochemistry, 57(7), 1210-1. https://doi.org/10.1271/bbb.57.1210
Nakazawa, H, et al. "Enzymatic Preparation of Aromatic Ethylamines from Aromatic L-Amino Acids." Bioscience, biotechnology, and biochemistry vol. 57,7 (1993): 1210-1. doi: https://doi.org/10.1271/bbb.57.1210
Nakazawa H, Sano K, Matsuda K, Mitsugi K. Enzymatic Preparation of Aromatic Ethylamines from Aromatic L-Amino Acids. Biosci Biotechnol Biochem. 1993 Jan;57(7):1210-1. doi: 10.1271/bbb.57.1210. PMID: 27281009.
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Showing 13 to 18 of 18 entries