Relevant bibliographies by topics / Reaction bischler napieralski

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Academic literature on the topic 'Reaction bischler napieralski'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Reaction bischler napieralski"

1

Puerto Galvis, Carlos, Mario Macías, and Vladimir Kouznetsov. "Unexpected PF6 Anion Metathesis during the Bischler–Napieralski Reaction: Synthesis of 3,4-Dihydroisoquinoline Hexafluorophosphates and Their Tetrahydroisoquinoline Related Alkaloids." Synthesis 51, no. 09 (2019): 1949–60. http://dx.doi.org/10.1055/s-0037-1610684.

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A series of N-phenethylcinnamamides were subjected to the Bischler–Napieralski reaction to furnish diverse 1-styryl-3,4-dihydroisoquinolines. We noticed that the desired products were unstable when the reaction was performed under conventional solvent conditions. However, when [bmim]PF6 was used as the reaction media, the nature of the Bischler–Napieralski reaction promoted an unusual in situ ionic interchange between this ionic liquid and the dihydroisoquinoline core that led to the stabilization of the desired 1-styryl-3,4-dihydroisoquinolines, allowing their isolation as hexafluorophosphate
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2

Kim, Kyung-Hee, and Cheol-Hong Cheon. "Concise catalytic asymmetric total syntheses of ancistrocladinium A and its atropdiastereomer." Organic Chemistry Frontiers 4, no. 7 (2017): 1341–49. http://dx.doi.org/10.1039/c7qo00195a.

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3

Ishikawa, Tsutomu, Tatsuru Saito, and Makoto Yoshida. "Triphosgene: A Versatile Reagent for Bischler-Napieralski Reaction." HETEROCYCLES 54, no. 1 (2001): 437. http://dx.doi.org/10.3987/com-00-s(i)44.

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4

Ramesh, D., and M. Srinivasan. "Phosphonitrilic Chloride - A Reagent for Bischler-Napieralski Reaction." Synthetic Communications 16, no. 12 (1986): 1523–27. http://dx.doi.org/10.1080/00397918608056405.

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5

Abu-Safieh, Kayed A., Mustafa M. El-Abadelah, Salim S. Sabri, Wolfgang Voelter, Cäcilia M. Mössmer та Markus Stroebele. "Bischler-Napieralski Synthesis of Some New Pyrazole-Fused β-Carbolines". Zeitschrift für Naturforschung B 57, № 11 (2002): 1327–32. http://dx.doi.org/10.1515/znb-2002-1120.

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3-(4-Acylaminopyrazol-5-yl)-4-methylindoles (13a,b), under Bischler-Napieralski reaction conditions, undergo cyclization at the pyrrolic carbon-2 with ultimate formation of the corresponding pyrazolo[3,4:5′,6′]pyrido[3,4-b]indoles (14a,b) as evidenced by crystal structure analysis of 14a.
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6

Muratov, A. V., S. A. Grebenyuk, and A. B. Eresko. "Synthesis of 1,2-Diazepines by the Bischler–Napieralski Reaction." Russian Journal of Organic Chemistry 54, no. 6 (2018): 861–66. http://dx.doi.org/10.1134/s1070428018060064.

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7

Meruva, Suresh Babu, Akula Raghunadh, Raghavendra Rao Kamaraju, U. K. Syam Kumar та P. K. Dubey. "An oxidative amidation and heterocyclization approach for the synthesis of β-carbolines and dihydroeudistomin Y". Beilstein Journal of Organic Chemistry 10 (25 лютого 2014): 471–80. http://dx.doi.org/10.3762/bjoc.10.45.

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A novel synthetic methodology has been developed for the synthesis of dihydro-β-carboline derivatives employing oxidative amidation–Bischler–Napieralski reaction conditions using tryptamine and 2,2-dibromo-1-phenylethanone as key starting materials. A number of dihydro-β-carboline derivatives have been synthesized in moderate to good yields using this methodology. Attempts were made towards the conversion of these dihydro-β-carbolines to naturally occurring eudistomin alkaloids.
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8

Han, Yi, Zhenzhu Hu, Meifang Liu, Mengwei Li, Tingting Wang, and Yulan Chen. "Synthesis, Characterization, and Properties of Diazapyrenes via Bischler–Napieralski Reaction." Journal of Organic Chemistry 84, no. 7 (2019): 3953–59. http://dx.doi.org/10.1021/acs.joc.8b03096.

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9

Syam Kumar, U., R. Shankar, Satish More, M. Madhubabu, and N. Vembu. "Synthesis of Isoquinoline Alkaloids via Oxidative Amidation-Bischler-Napieralski Reaction." Synlett 23, no. 07 (2012): 1013–20. http://dx.doi.org/10.1055/s-0031-1290655.

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10

Saito, Tatsuru, Makoto Yoshida, and Tsutomu Ishikawa. "ChemInform Abstract: Triphosgene: A Versatile Reagent for Bischler-Napieralski Reaction." ChemInform 32, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.200123139.

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