Relevant bibliographies by topics / N-Dibenzylaminen

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'N-Dibenzylaminen'

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

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-Dibenzylaminen.'

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-Dibenzylaminen"

1

Craig, F. J., A. R. Kennedy, and R. E. Mulvey. "Chloro(dibenzylamine-N)dimethylaluminium(III)." Acta Crystallographica Section C Crystal Structure Communications 54, no. 3 (1998): 335–37. http://dx.doi.org/10.1107/s010827019701679x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Hungerhoff, Benno, Subhendu S. Samanta, Jochen Roels, and Peter Metz. "ChemInform Abstract: Chemoselective Oxidative Debenzylation of N,N-Dibenzylamines." ChemInform 31, no. 17 (2010): no. http://dx.doi.org/10.1002/chin.200017064.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Shajari, Nahid, Reza Kazemizadeh, and Ali Ramazani. "Efficient one-pot, four-component synthesis of N,N-dibenzyl-N-{1-[5-(3-aryl)-1,3,4-oxadiazol-2-yl]cyclobutyl}amine derivatives from the reaction of (isocyanoimino)triphenylphosphorane, dibenzylamine, an aromatic carboxylic acid and cyclobutanone." Journal of the Serbian Chemical Society 77, no. 9 (2012): 1175–80. http://dx.doi.org/10.2298/jsc111014024s.

Full text
Abstract:
Four-component reaction of cyclobutanone, dibenzylamine and (Nisocyanimino) triphenylphosphorane in the presence of aromatic carboxylic acids proceed smoothly at room temperature and under neutral conditions to afford N,N-dibenzyl-N-{1-[5-(3-aryl)-1,3,4-oxadiazol-2-yl]cyclobutyl}amine derivatives in high yields.
APA, Harvard, Vancouver, ISO, and other styles
4

Siqintuya, Yoshimi Sueishi, and Shunzo Yamamoto. "Solvent-dependent intramolecular exciplex formation of N-benzyl-N-methylamine and N,N-dibenzylamine." Journal of Photochemistry and Photobiology A: Chemistry 186, no. 1 (2007): 41–46. http://dx.doi.org/10.1016/j.jphotochem.2006.07.010.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Beşli, Serap, Simon J. Coles, David B. Davies, et al. "Structural investigations of phosphorus–nitrogen compounds. 4. Steric and electronic effects in dibenzylamino derivatives of hexachlorocyclotriphosphazatriene and 4,4,6,6-tetrachloro-2,2-diphenylcyclotriphosphazatriene." Acta Crystallographica Section B Structural Science 58, no. 3 (2002): 545–52. http://dx.doi.org/10.1107/s0108768102003816.

Full text
Abstract:
A systematic study is presented on the products of aminolysis of N3P3Cl6 (1) and N3P3Ph2Cl4 (4) with dibenzylamine. Two series of mono- and disubstituted derivatives of compounds (1) and (4), namely N3P3Cl5[N(CH2Ph)2] (2) and N3P3Cl4[N(CH2Ph)2]2 (3) and N3P3Ph2Cl3[N(CH2Ph)2] (5) and N3P3Ph2Cl2[N(CH2Ph)2]2 (6) [where (2), (3), (5) and (6) are new structures], are investigated in order to determine whether steric or electronic effects prevail in the formation of dibenzylamino-substituted cyclophosphazenes. The influence of an electron-releasing group (i.e. phenyl) on the stereochemistry and degr
APA, Harvard, Vancouver, ISO, and other styles
6

Pavlenko, Natalia V., Tatiana I. Oos, Yurii L. Yagupolskii, Igor I. Gerus, Uwe Doeller та Lothar Willms. "A novel family of (1-aminoalkyl)(trifluoromethyl)- and -(difluoromethyl)phosphinic acids – analogues of α-amino acids". Beilstein Journal of Organic Chemistry 10 (26 березня 2014): 722–31. http://dx.doi.org/10.3762/bjoc.10.66.

Full text
Abstract:
A series of novel (1-aminoalkyl)(trifluoromethyl)- and -(difluoromethyl)phosphinic acids – analogues of proteinogenic and nonproteinogenic α-amino acids were prepared. The synthetic methodology was based on nucleophilic addition of (trifluoromethyl)phosphinic acid or (difluoromethyl)phosphinic acid or its ethyl ester to substrates with C=N or activated C=C double bonds. Analogues of glycine, phenylglycine, alanine, valine, proline, aminomalonic and aspartic acids were thus prepared. Three-component one-pot reactions of (trifluoromethyl)phosphinic acid and dibenzylamine with aldehydes were also
APA, Harvard, Vancouver, ISO, and other styles
7

Lim, Suk Hyun, Jinju Yi, Choon Sup Ra та ін. "SET-promoted photoaddition reactions of N -α-trimethylsilylmethyl- N , N -dibenzylamines with fullerene C 60 . Electronic factors that govern photoaddition efficiencies". Tetrahedron Letters 56, № 23 (2015): 3014–18. http://dx.doi.org/10.1016/j.tetlet.2014.10.060.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Szakonyi, Zsolt, Reijo Sillanpää та Ferenc Fülöp. "Stereoselective synthesis of perillaldehyde-based chiral β-amino acid derivatives through conjugate addition of lithium amides". Beilstein Journal of Organic Chemistry 10 (21 листопада 2014): 2738–42. http://dx.doi.org/10.3762/bjoc.10.289.

Full text
Abstract:
The Michael addition of dibenzylamine to (+)-tert-butyl perillate (3) and to (+)-tert-butyl phellandrate (6), derived from (S)-(−)-perillaldehyde (1), resulted in diastereomeric β-amino esters 7A–D in a moderately stereospecific reaction in a ratio of 76:17:6:1. After separation of the diastereoisomers, the major product, cis isomer 7A, was quantitatively isomerized to the minor component, trans-amino ester 7D. All four isomers were transformed to the corresponding β-amino acids 10A–D, which are promising building blocks for the synthesis of β-peptides and 1,3-heterocycles in three steps. The
APA, Harvard, Vancouver, ISO, and other styles
9

Donevan, Sean D., H. Steve White, Gail D. Anderson та Jong M. Rho. "Voltage-Dependent Block of N-Methyl-d-Aspartate Receptors by the Novel Anticonvulsant Dibenzylamine, a Bioactive Constituent of l-(+)-β-Hydroxybutyrate". Epilepsia 44, № 10 (2003): 1274–79. http://dx.doi.org/10.1046/j.1528-1157.2003.07203.x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Fischer, Malte, Kerstin Fitschen, Marc Schmidtmann та Rüdiger Beckhaus. "Reactivity Studies of a Bis(π-η5:σ-η1-benzofulvene)titanium Complex Including Simultaneous N–H and C(sp2)–H Activation of Dibenzylamine". Organometallics 38, № 19 (2019): 3760–67. http://dx.doi.org/10.1021/acs.organomet.9b00487.

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

Dissertations / Theses on the topic "N-Dibenzylaminen"

1

Roels, Jochen. "Beiträge zur Synthese von Modellsystemen des heterobicyclischen Grundgerüstes der Saragossasäuren/Squalestatine sowie methodische Untersuchungen zur chemoselektiven mono-Debenzylierung von N,N-Dibenzylaminen und katalytischen enantioselektiven Ringöffnung von meso-Epoxiden." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2000. http://nbn-resolving.de/urn:nbn:de:swb:14-994697037140-73077.

Full text
Abstract:
Es wurden Untersuchungen zur Synthese von Modellsystemen des heterobicyclischen Grundgerüsts der Saragossasäuren/Squalestatine durch Acetalisierung unterschiedlich konfigurierter acyclischer Diketohexaole durchgeführt. In diesem Zusammenhang gelang die biderektionale Darstellung eines Modellsystems in sieben Stufen mit einer Gesamtausbeute von 34 %. Als Methode zur Etablierung der korrekten Konfiguration der Hydroxygruppen diente die asymmetrische Dihydroxylierung nach Sharples. In einem weiteren Teil der Arbeit wurde die selektive mono-Debenzylierung verschiedener N,N-Dibenzylamine mit Cer(IV
APA, Harvard, Vancouver, ISO, and other styles
2

Roels, Jochen [Verfasser]. "Beiträge zur Synthese von Modellsystemen des heterobicyclischen Grundgerüstes der Saragossasäuren, Squalestatine sowie methodische Untersuchungen zur chemoselektiven Mono-Debenzylierung von N,N-Dibenzylaminen und katalytischen enantioselektiven Ringöffnung von Meso-Epoxiden / Jochen Roels." 2000. http://d-nb.info/962683213/34.

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

Conference papers on the topic "N-Dibenzylaminen"

1

Vieira, Daniel Pais Pires, Leandro Lara de Carvalho, and Vera Lúcia Patrocinio Pereira. "Diastereoselective Multicomponent [4+2]/[3+2] Cycloadditions of gamma-(S)-N,N-dibenzylamine Nitroalkenes Derivatives with Ethyl Vinyl Ether (EVE) and Electron-Poor Alkenes Using Li+- Containing Catalysts." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0138-2.

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