Relevant bibliographies by topics / Asymmetric aziridination

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Asymmetric aziridination'

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 'Asymmetric aziridination.'

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 "Asymmetric aziridination"

1

Pellissier, Hélène. "Recent developments in asymmetric aziridination." Tetrahedron 66, no. 8 (2010): 1509–55. http://dx.doi.org/10.1016/j.tet.2009.11.089.

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

Pellissier, Hélène. "Recent Developments in Asymmetric Aziridination." Advanced Synthesis & Catalysis 356, no. 9 (2014): 1899–935. http://dx.doi.org/10.1002/adsc.201400312.

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

Roma, Elia, Eleonora Tosi, Martina Miceli, and Tecla Gasperi. "Asymmetric Organocatalytic Aziridination: Recent Advances." Asian Journal of Organic Chemistry 7, no. 12 (2018): 2357–67. http://dx.doi.org/10.1002/ajoc.201800431.

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

Pesciaioli, Fabio, Francesco De Vincentiis, Patrizia Galzerano, et al. "Organocatalytic Asymmetric Aziridination of Enones." Angewandte Chemie 120, no. 45 (2008): 8831–34. http://dx.doi.org/10.1002/ange.200803647.

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

Pesciaioli, Fabio, Francesco De Vincentiis, Patrizia Galzerano, et al. "Organocatalytic Asymmetric Aziridination of Enones." Angewandte Chemie International Edition 47, no. 45 (2008): 8703–6. http://dx.doi.org/10.1002/anie.200803647.

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

Wipf, Peter, and Michael A. Lyon. "Catalytic asymmetric aziridination of aryl imines." Arkivoc 2007, no. 12 (2007): 91–98. http://dx.doi.org/10.3998/ark.5550190.0008.c07.

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

Kawabata, H., K. Omura, and T. Katsuki. "Ru(II)-Salen-Catalyzed Asymmetric Aziridination." Synfacts 2006, no. 5 (2006): 0457. http://dx.doi.org/10.1055/s-2006-934349.

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

De Vincentiis, Francesco, Giorgio Bencivenni, Fabio Pesciaioli, et al. "Asymmetric Catalytic Aziridination of Cyclic Enones." Chemistry - An Asian Journal 5, no. 7 (2010): 1652–56. http://dx.doi.org/10.1002/asia.201000040.

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

Gupta, Anil K., Munmun Mukherjee, and William D. Wulff. "Multicomponent Catalytic Asymmetric Aziridination of Aldehydes." Organic Letters 13, no. 21 (2011): 5866–69. http://dx.doi.org/10.1021/ol202472z.

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

Wulff, William D., Yong Guan, Zhenjie Lu, Xiaopeng Yin, Aliakbar Mohammadlou, and Richard J. Staples. "Catalytic Asymmetric Aziridination of Benzhydryl Imines and Diazoacetate­ Esters with BOROX Catalysts from 3,3′-Disubstituted VANOL Ligands." Synthesis 52, no. 14 (2020): 2073–91. http://dx.doi.org/10.1055/s-0039-1690860.

Full text
Abstract:
This work details the synthesis of 22 new chiral VANOL ligands that differ by the nature of the substituent in the 3- and 3′-positions of the ligand. These ligands were incorporated into boroxinate catalysts that were used to screen the catalytic asymmetric aziridination of benzhydryl imines with ethyl diazoacetate. Each catalyst was screened in the reaction of imines generated from benzaldehyde and cyclohexanecarboxaldehyde and some with 4-nitro- and 4-methoxybenzaldehyde. In addition, the first report of the effect of the ester substituent of the diazoacetate ester on the asymmetric inductio
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Asymmetric aziridination"

1

Tughan, Garfield Cecil. "Asymmetric aziridination of alkenes." Thesis, University of Leicester, 1987. http://hdl.handle.net/2381/33961.

Full text
Abstract:
The work contained in this thesis is essentially concerned with the development of methods for the asymmetric aziridination of prochiral alkenes using N-nitrenes. The studies carried out are a necessary first step in a strategy directed towards the enantiospecific functionalization of alkenes. The addition of the N-nitrenes derived by oxidation of the chiral 1-amino-2-(l ,2,2-trimethylpropyl) benzimidazole and chiral 3-amino-2-(l,2,2-trimethylpropyl)quinazolin-4 (3H)-one (in the presence of TFA) to prochiral alkenes are found to proceed with moderate to high diastereoselectivities. The asymmet
APA, Harvard, Vancouver, ISO, and other styles
2

Wincewicz, Richard Charles. "Towards an organocatalytic asymmetric aziridination of enones." Thesis, Imperial College London, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501766.

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

Wang, Ziyu, та 汪子玉. "Organocatalytic asymmetric synthesis of dihydrodibenzofurans and asymmetric aziridination of α-nitroalkenes". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hdl.handle.net/10722/193388.

Full text
Abstract:
The synthesis of useful chiral skeletons from simple achiral starting materials is always the dream of organic chemists. In the past decades, organocatalysis has been rapidly developed and has become one of the most important methods in asymmetric catalysis. The aim of this thesis is to develop asymmetric methods for the construction of useful chiral skeletons based on organocatalytic chemistry. Many natural products and biologically important compounds contain the hydrogenated dibenzofuran (Figure 1) as a common sub-structure. In the first part of this thesis, the first amine-catalysed asymm
APA, Harvard, Vancouver, ISO, and other styles
4

Bordogna, Celine. "New reagents for electrophilic amination and asymmetric aziridination." Thesis, University of East Anglia, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522283.

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

Liu, Renmao. "Asymmetric dihydroxylation and aziridination of allenes and related chemestry /." Diss., CLICK HERE for online access, 2007. http://contentdm.lib.byu.edu/ETD/image/etd1843.pdf.

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

Liu, Renmao. "Asymmetric Dihydroxylation and Aziridination of Allenes and Related Chemistry." BYU ScholarsArchive, 2007. https://scholarsarchive.byu.edu/etd/899.

Full text
Abstract:
A novel method for asymmetric synthesis of α-hydroxy ketone with excellent regio- and stereoselectivity has been established by the systematic investigation of asymmetric dihydroxylation of allenes. The efficiency of kinetic resolution of racemic allenes was also investigated by using the AD reaction on both 1,3-disubstituted and trisubstituted allenes. Steric effects, electronic effects and allene substitution are also discussed. Aziridines were formed by copper-catalyzed intramolecular nitrene addition to alkenes. The carbamate group was used as the tether between the alkene and the nitrene.
APA, Harvard, Vancouver, ISO, and other styles
7

Sunose, Mihiro. "Asymmetric methods for functionalisation of nitrogen heterocycles." Thesis, University of Bristol, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297768.

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

Harm, A. M. "Chiral ligands for asymmetric metal-catalysed additions to alkenes." Thesis, University of Newcastle Upon Tyne, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318258.

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

Jeffs, Laura Ellen. "Heterogeneous asymmetric aziridination of styrene using Cu2+ exchanged zeolite Y." Thesis, Cardiff University, 2009. http://orca.cf.ac.uk/55128/.

Full text
Abstract:
By synthesising S-2-phenyl-Af-(4-nitrophenyl)aziridine from S-phenylglycinol, it has been demonstrated that the aziridination of styrene by N-(4- nitrobenzenesulfonyl)imino phenyliodinane, (nosyliminophenyliodinane, PhlNNs) in the presence of tS',AS'-2,2,-isopropylidene-bis(4-phenyl-2-oxazoline), catalysed by copper(II) triflate in CH3CN solution or heterogeneously by CuHY, has predominantly an /-configuration. The enantioselectivity of the aziridination of styrene by Af-arenesulfonylimino-phenyliodinanes catalysed by copper-exchanged zeolite Y (CuHY), in conjunction with a chiral bis-oxazolin
APA, Harvard, Vancouver, ISO, and other styles
10

Lu, Zhenjie. "Studies on the optimization of catalytic asymmetric aziridination reaction tactics and mechanism /." Diss., Connect to online resource - MSU authorized users, 2008.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Asymmetric aziridination"

1

Charette, André B., Hélène Lebel, and Marie-Noelle Roy. "Asymmetric Cyclopropanation and Aziridination Reactions." In Copper-Catalyzed Asymmetric Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch8.

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

Aggarwal, Varinder K., J. Gair Ford, Alison Thompson, John Studley, Ray V. H. Jones, and Robin Fieldhouse. "Sulfur Ylide Mediated Catalytic Asymmetric Epoxidation and Aziridination." In Current Trends in Organic Synthesis. Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4801-0_24.

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

"Asymmetric Aziridination." In Asymmetric Synthesis of Three-Membered Rings. Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527802029.ch2.

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

Muchalski, H., and J. N. Johnston. "Asymmetric Aziridination Using CuHY Zeolites." In Stereoselective Synthesis 1 Stereoselective Reactions of Carbon—Carbon Double Bonds. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-201-00086.

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

Conference papers on the topic "Asymmetric aziridination"

1

Chaves, Humberto T., Ana M. Lobo, Sundaresan Prabhakar, and Henry S. Rzepa. "A theoretical mechanistic investigation of asymmetric aziridination by N-Aryl-O-acylhydroxylamines." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47868.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Asymmetric aziridination' for particular source types:
Journal articles Dissertations / Theses
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