Relevant bibliographies by topics / Acylaziridines

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Acylaziridines'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 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 'Acylaziridines.'

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 "Acylaziridines"

1

Rubin, Heather, Jennifer Cockrell, and Jeremy B. Morgan. "Scalable Synthesis ofN-Acylaziridines fromN-Tosylaziridines." Journal of Organic Chemistry 78, no. 17 (2013): 8865–71. http://dx.doi.org/10.1021/jo401267j.

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

Pankova, Alena, and Mikhail Kuznetsov. "Recent Advances in the Chemistry of 2-Acylaziridines." Synthesis 49, no. 23 (2017): 5093–104. http://dx.doi.org/10.1055/s-0036-1590889.

Full text
Abstract:
This review highlights recent achievements in the transformations of 2-acylaziridines toward the synthesis of cyclic and acyclic nitrogen-containing compounds. The influence of a carbonyl group on reaction selectivity is discussed.1 Introduction2 Reactions via C–C Bond Cleavage3 Reactions via C–N Bond Cleavage3.1 Reactions Starting with the Aziridine Ring Opening3.2 Reactions Starting at the Carbonyl Group4 Conclusion
APA, Harvard, Vancouver, ISO, and other styles
3

Tangara, Salia, Alice Kanazawa, and Sandrine Py. "The Baldwin Rearrangement: Synthesis of 2-Acylaziridines." European Journal of Organic Chemistry 2017, no. 43 (2017): 6357–64. http://dx.doi.org/10.1002/ejoc.201700920.

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

Kim, Yongeun, Hyun-Joon Ha, Hoseop Yun, Baeck Kyoung Lee, and Won Koo Lee. "Ring opening of 2-acylaziridines by acid chlorides." Tetrahedron 62, no. 37 (2006): 8844–49. http://dx.doi.org/10.1016/j.tet.2006.06.025.

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

Gayon, Eric, Olivier Debleds, Marie Nicouleau, et al. "Highly Diastereoselective Baldwin Rearrangement of Isoxazolines intocis-Acylaziridines." Journal of Organic Chemistry 75, no. 17 (2010): 6050–53. http://dx.doi.org/10.1021/jo101273d.

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

Cockrell, Jennifer, Christopher Wilhelmsen, Heather Rubin, Allen Martin, and Jeremy B. Morgan. "Enantioselective Synthesis and Stereoselective Ring Opening ofN-Acylaziridines." Angewandte Chemie International Edition 51, no. 39 (2012): 9842–45. http://dx.doi.org/10.1002/anie.201204224.

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

Cockrell, Jennifer, Christopher Wilhelmsen, Heather Rubin, Allen Martin, and Jeremy B. Morgan. "Enantioselective Synthesis and Stereoselective Ring Opening ofN-Acylaziridines." Angewandte Chemie 124, no. 39 (2012): 9980–83. http://dx.doi.org/10.1002/ange.201204224.

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

Ward, Virginia R., Matthew A. Cooper та A. David Ward. "Synthesis of N-acylaziridines from β-amido selenides". Journal of the Chemical Society, Perkin Transactions 1, № 9 (2001): 944–45. http://dx.doi.org/10.1039/b102468j.

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

Mita, Tsuyoshi, Ikuo Fujimori, Reiko Wada, Jianfeng Wen, Motomu Kanai, and Masakatsu Shibasaki. "Catalytic Enantioselective Desymmetrization ofmeso-N-Acylaziridines with TMSCN." Journal of the American Chemical Society 127, no. 32 (2005): 11252–53. http://dx.doi.org/10.1021/ja053486y.

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

Yook, Cheol-Min, Hee-Sung Eum, Hyun-Joon Ha, Kyung-Yeon Kang, and Won-Koo Lee. "Regiochemical Pathway in the Ring Opening of 2-Acylaziridines." Bulletin of the Korean Chemical Society 32, spc8 (2011): 2879–80. http://dx.doi.org/10.5012/bkcs.2011.32.8.2879.

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

Dissertations / Theses on the topic "Acylaziridines"

1

Debleds, Olivier. "Substitutions propargyliques : méthodologie & développements synthétiques." Montpellier 2, 2009. http://www.theses.fr/2009MON20159.

Full text
Abstract:
Le travail présenté dans ce manuscrit concerne le développement de nouvelles réactions utilisant la substitution propargylique par des complexes d'or (III) et de fer (III). En premier lieu, une exploration du champ d'application de cette méthodologie a été réalisée, ce qui a conduit par la suite, à la mise au point de nouvelles méthodes d'accès aux 2,3-dihydroisoxazoles, aux isoxazoles et ainsi qu'aux acylaziridines. Enfin, le développement d'une nouvelle méthodologie d'accès aux cycles à quatre chaînons par métathèse a pu être exploré<br>The work reported in this manuscript concerned the deve
APA, Harvard, Vancouver, ISO, and other styles
2

Hamm, Sandrine. "Développement de pro insecticides potentiels d'acides carboxyliques, basés sur les structures 2-oxazolines, 2-thiazolines et n-acylaziridines : suivis directs dans les milieux biologiques d'insecte par RMN 1 9f et HPLC : réactivité des 2-oxazolines et des 2-thiazolines avec le 4,6-dinitrobenzofuroxane." Versailles-St Quentin en Yvelines, 1999. http://www.theses.fr/1999VERS0012.

Full text
Abstract:
Les @ 2-oxazolines, 2-thiazolines et n-acylaziridines sont étudiées comme structures de pro insecticides d'acides carboxyliques fluorés (principes actifs. Les 2-oxazolines ont été obtenues soit par réarrangement des n-acylaziridines correspondantes, soit par condensation d'un acide carboxylique active et d'une -ethanolamine. La réactivité du carbone en de la position 2 des 2-oxazolines et des 2-thiazolines a été abordée lors de leur metallation/alkylation et par leur réaction de condensation avec un électrophile fort : le 4,6-dinitrobenzofuroxane. Les proprietes biologiques de ces composés ont
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Acylaziridines"

1

Gallego, Mar Gómez, and Miguel A. Sierra. "Level 2 — Case 31 Stereoselective Synthesis of 2-Acylaziridines." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_31.

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

Smith, M. B. "Aza-Claisen Rearrangement of Acylaziridines." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00690.

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

Yun, Jung Min, Taebo Sim, Heung Sik Hahm, Won Koo Lee, and Hyun-Joon Ha. "Stereoselective Reduction of 2-Acylaziridines: An Efficient Synthesis of D-erythro- Sphinganine and Safingol From a Common Intermediate." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50217-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Acylaziridines' 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