Relevant bibliographies by topics / N-benzyl anilines

Contents

  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'N-benzyl anilines'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'N-benzyl anilines.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "N-benzyl anilines"

1

Neeraj, Rani, R. Sharma J., K. Kaul V., and R. Manrao M. "Secondary amines : Synthesis and effect of length of spacer linking two phenyl rings on biological activity." Journal of Indian Chemical Society Vol. 85, Oct 2008 (2008): 1041–44. https://doi.org/10.5281/zenodo.5820670.

Full text
Abstract:
Department of Chemistry, Department of Plant Pathology, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>Manuscript received 7 January 2008, revised 30 June 2008, accepted 16 July 2008</em> N-Benzyl benzylamines (1a-11a) and N-benzyl anilines (1b-11b) were synthesized by sodium borohydride reduction of aldimines of benzylamine and aniline respectively. The products were characterized on the basis of elemental analysis and spectral studies and screened for antifungal potential against four fungi and evaluated for nematicidal activity against two nematodes. The former compound
APA, Harvard, Vancouver, ISO, and other styles
2

Li, Lu, Na Li, Xiao-Tian Mo, Ming-Wei Yuan, Lin Jiang, and Ming-Long Yuan. "Synthesis of 2-benzyl N-substituted anilines via imine condensation–isoaromatization of (E)-2-arylidene-3-cyclohexenones and primary amines." Beilstein Journal of Organic Chemistry 20 (July 2, 2024): 1468–75. http://dx.doi.org/10.3762/bjoc.20.130.

Full text
Abstract:
A catalyst- and additive-free synthesis of 2-benzyl N-substituted anilines from (E)-2-arylidene-3-cyclohexenones and primary amines has been reported. The reaction proceeds smoothly through a sequential imine condensation–isoaromatization pathway, affording a series of synthetically useful aniline derivatives in acceptable to high yields. Mild reaction conditions, no requirement of metal catalysts, operational simplicity and the potential for scale-up production are some of the highlighted advantages of this transformation.
APA, Harvard, Vancouver, ISO, and other styles
3

Pati, Hari, Paul Weisbruch, Adrienne Lemon, and Moses Lee. "Synthesis of N‐Benzylated Anilines from the Reaction of Anilines and Benzyl Chloroformate." Synthetic Communications 34, no. 5 (2004): 933–40. http://dx.doi.org/10.1081/scc-120028366.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Goyal, Vishakha, Naina Sarki, Mukesh Kumar Poddar, et al. "Biorenewable carbon-supported Ru catalyst for N-alkylation of amines with alcohols and selective hydrogenation of nitroarenes." New Journal of Chemistry 45, no. 32 (2021): 14687–94. http://dx.doi.org/10.1039/d1nj01654g.

Full text
Abstract:
A renewable carbon-supported Ru catalyst (Ru/PNC-700) facilely prepared via simple impregnation followed by the pyrolysis process for N-alkylation of anilines with benzyl alcohol and chemoselective hydrogenation of nitroarenes.
APA, Harvard, Vancouver, ISO, and other styles
5

Qiao, Mengjun, Jinli Zhang, Ling Chen та ін. "Transition metal-free α-Csp3–H oxidative sulfuration of benzyl thiosulfates with anilines to form N-aryl thioamides". Organic & Biomolecular Chemistry 17, № 15 (2019): 3790–96. http://dx.doi.org/10.1039/c9ob00336c.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Dubey, Pooja, Sonu Gupta та Ajai K. Singh. "Base free N-alkylation of anilines with ArCH2OH and transfer hydrogenation of aldehydes/ketones catalyzed by the complexes of η5-Cp*Ir(iii) with chalcogenated Schiff bases of anthracene-9-carbaldehyde". Dalton Transactions 47, № 11 (2018): 3764–74. http://dx.doi.org/10.1039/c7dt04326k.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Štěpnička, Petr, Tomáš Baše, Ivana Císařová, Jiří Kubišta, Štěpán Vyskočil, and Martin Štícha. "Synthesis and Catalytic Activity of Spaced Ferrocene Oxazolines." Collection of Czechoslovak Chemical Communications 68, no. 7 (2003): 1206–32. http://dx.doi.org/10.1135/cccc20031206.

Full text
Abstract:
Chiral 2-[{N-aryl-N-(ferrocenylmethyl)amino}methyl]-4-(1-methylethyl)-4,5-dihydroxazoles with various substituents at the aryl ring were prepared by alkylation of N-(ferrocenylmethyl)anilines, FcCH2NHC6H4R (Fc = ferrocenyl), with (S)-2-(chloromethyl)-4-(1-methylethyl)-4,5-dihydrooxazole. The oxazoles, substituted anilines, and the precursors of the latter, the respective Schiff bases FcCH=NC6H4R, were characterized by standard methods and further studied by mass spectrometry. The oxazoles were further tested as chiral auxiliaries in the addition of diethylzinc to benzaldehyde but showed only n
APA, Harvard, Vancouver, ISO, and other styles
8

Gorrod, John W., та Nigel J. Gooderham. "Improved Preparation of α,N-Diphenylnitrones andN-Benzyl-N-Phenylhydroxylamines by direct Oxidation of Secondary Anilines". Archiv der Pharmazie 319, № 3 (1986): 261–65. http://dx.doi.org/10.1002/ardp.19863190313.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Al Mamari, Hamad H. "Ir-Catalyzed ortho-C-H Borylation of Aromatic C(sp2)-H Bonds of Carbocyclic Compounds Assisted by N-Bearing Directing Groups." Reactions 5, no. 2 (2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.

Full text
Abstract:
C-H borylation is a powerful strategy for the construction of C-B bonds due to the synthetic versatility of C-B bonds. Various transition metals affect the powerful functionalization of C-H bonds, of which Ir is the most common. Substrate-directed methods have enabled directed Ir-catalyzed C-H borylation at the ortho position. Amongst the powerful directing groups in Ir-catalyzed C-H borylation are N-containing carbocyclic systems. This review covers substrate-directed Ir-catalyzed ortho-C-H borylation of aromatic C(sp2)-H bonds in N-containing carbocyclic compounds, such as anilines, amides,
APA, Harvard, Vancouver, ISO, and other styles
10

Laha, Joydev K., Pankaj Gupta, and Amitava Hazra. "Sulfate radical anion-induced benzylic oxidation of N-(arylsulfonyl)benzylamines to N-arylsulfonylimines." Beilstein Journal of Organic Chemistry 19 (June 5, 2023): 771–77. http://dx.doi.org/10.3762/bjoc.19.57.

Full text
Abstract:
A mild, operationally convenient, and practical method for the synthesis of synthetically useful N-arylsulfonylimines from N-(arylsulfonyl)benzylamines using K2S2O8 in the presence of pyridine as a base is reported herein. In addition, a “one-pot” tandem synthesis of pharmaceutically relevant N-heterocycles by the reaction of N-arylsulfonylimines, generated in situ with ortho-substituted anilines is also reported. The key features of the protocol include the use of a green oxidant, a short reaction time (30 min), chromatography-free isolation, scalability, and economical, delivering N-arylsulf
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "N-benzyl anilines"

1

Huang, An-Cheng, and 黃安正. "Synthesis and Biological Activity of Certain Ethyl 2-[N-various Substituted benzyl]Substituted anilino-4-oxo-4,5-dihydrofuran-3-carboxylate." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/69772011086807761891.

Full text
Abstract:
博士<br>中國醫藥大學<br>藥物化學研究所博士班<br>95<br>One series of ethyl 2-(substituted anilino)-4-oxo-4,5-dihydrofuran-3-carboxylate (1~10), multi-series of ethyl 2-[N-various benzyl] substituted anilino-4-oxo-4,5-dihydro-furan -3-carboxylate (11~151), One series of N-various benzyl-7-methoxy-2,3,4,9-tetrahydrofuro- [2,3-b]-quinolin-3,4-diones (155~167) and another series of N-various benzyl-7-methoxy- 4,9-dihydrofuro[2,3-b]quinolin-4-diones (169~180) have been synthesized and assessed their chemical structures by their spectra data. All of these synthetic compound were evaluated for biological activities. In
APA, Harvard, Vancouver, ISO, and other styles
2

Huang, Shih-Ming, and 黃士鳴. "Synthesis and Biological Activity of Ethyl 2-{N-substituted benzyl-[2'-fluoro(or methoxy)]}anilino-4-oxo-4,5-dihydrofuran-3-carboxylate." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/92983984445905645428.

Full text
Abstract:
碩士<br>中國醫藥大學<br>藥物化學研究所<br>92<br>A series of ethyl 2-{N-substituted benzyl- [2'-fluoro(or methoxy)]}anilino-4-oxo-4,5-dihydrofuran-3-carboxylate and related compounds has been synthesized and assigned by their spectra data. All of these synthetic compounds were evaluated for anti-arrhythmias activity and cardiovascular effect. Among the investigations of the inhibitory effect on the heart rate , ethyl 2-[N- benzyl-(2'-fluoro)]anilino-4-oxo-4,5-dihydrofuran-3-carboxylate（2）was found to exhibit the most significant activities at 30μM while pacermaker S.A. node was inhibited at concent
APA, Harvard, Vancouver, ISO, and other styles
3

朱瑞元. "Synthesis of Ethyl 2-[N-substituted benzyl-3-(or 4-)methoxy]anilino-4-oxo-4,5-dihydrofuran-3- carboxylate as Anticancer Agents." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/19775827190625320450.

Full text
Abstract:
碩士<br>中國醫藥大學<br>藥物化學研究所<br>92<br>As part of our continuing search for potential antimitotic agents and cytotoxicity agent, ethyl 2-(N-benzyl-2-anilino)-4-oxo-4,5-dihydrofuran- 3-carboxylate (5) was selected as the lead compound. The starting material diethyl malonate was added to sodium hydride which suspended in tetrahydrofuran, and then treated with chloroacetyl chloride to yield ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran- 3-carboxylate (i). The intermediate i was condensed with m- (or p-)anisidine to yield ethyl 2-(3-methoxyanilino)-4-oxo-4,5-dihydrofuran- 3-carboxylate (2) or ethyl 2
APA, Harvard, Vancouver, ISO, and other styles
4

Su, I. Fang, and 蘇怡芳. "Synthesis and Biological Activity of Ethyl 2-[N-substituted benzyl-4¢(or 3¢)-bromo]anilino-4-oxo-4,5-dihydro- furan-3-carboxylate." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/40810184770007644607.

Full text
Abstract:
碩士<br>中國醫藥大學<br>藥物化學研究所碩士班<br>94<br>A series of ethyl 2-[N-substituted benzyl- 4´(or 3´)-bromo]anilino- 4-oxo-4,5-dihydrofuran-3-carboxylate and related compounds has been synthesized and assigned by their spectra data. All of these synthetic compounds were evaluated for anti-arrhythmics activity and cardiovascular effect. Among the investigations of the inhibitory effect on the heart rate , Ethyl 2-[N-m-fluorobenzyl-(3´-bromo)]anilino-4-oxo-4,5-dihydrofuran-3-carboxylate （27）、Ethyl 2-[N-m-chlorobenzyl-(3´-bromo)]anilino-4-oxo-4,5-dihydro- furan-3-carboxylate（30）、Ethyl 2-[N- benzyl-(3´-bromo)]
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'N-benzyl anilines' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography