Relevant bibliographies by topics / Buchner reaction

Contents

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

Academic literature on the topic 'Buchner reaction'

Author: Grafiati
Published: 20 July 2024
Last updated: 31 July 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 'Buchner reaction.'

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 "Buchner reaction"

1

Wu, Yong-Jin. "ChemInform Abstract: Buchner Reaction." ChemInform 42, no. 30 (2011): no. http://dx.doi.org/10.1002/chin.201130264.

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

Liu, Yuxiao, Yongming Deng, Peter Y. Zavalij, Renhua Liu та Michael P. Doyle. "An efficient route to highly enantioenriched tetrahydroazulenes and β-tetralones by desymmetrization reactions of δ,δ-diaryldiazoaceto-acetates". Chemical Communications 51, № 3 (2015): 565–68. http://dx.doi.org/10.1039/c4cc08255a.

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

Phan Thi Thanh, Nga, Masaya Tone, Hayato Inoue, Ikuhide Fujisawa, and Seiji Iwasa. "Highly stereoselective intramolecular Buchner reaction of diazoacetamides catalyzed by a Ru(ii)–Pheox complex." Chemical Communications 55, no. 89 (2019): 13398–401. http://dx.doi.org/10.1039/c9cc06889a.

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

Mato, Mauro, and Antonio M. Echavarren. "Donor Rhodium Carbenes by Retro-Buchner Reaction." Angewandte Chemie 131, no. 7 (2019): 2110–14. http://dx.doi.org/10.1002/ange.201813512.

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

Mato, Mauro, and Antonio M. Echavarren. "Donor Rhodium Carbenes by Retro-Buchner Reaction." Angewandte Chemie International Edition 58, no. 7 (2019): 2088–92. http://dx.doi.org/10.1002/anie.201813512.

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

Lauterbach, Tobias, Takafumi Higuchi, Matthias W. Hussong, et al. "Gold-Catalyzed Carbenoid Transfer Reactions of Diynes - Pinacol RearrangementversusRetro-Buchner Reaction." Advanced Synthesis & Catalysis 357, no. 4 (2015): 775–81. http://dx.doi.org/10.1002/adsc.201400849.

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

Maguire, Anita R., N. Rachael Buckley, Patrick O’Leary, and George Ferguson. "Stereocontrol in the intramolecular Buchner reaction of diazoketones." Journal of the Chemical Society, Perkin Transactions 1, no. 24 (1998): 4077–92. http://dx.doi.org/10.1039/a807677d.

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

Mo, Shanyan, and Jiaxi Xu. "Chemospecific Intramolecular Buchner Reaction Catalyzed by Copper(II) Acetylacetonate." ChemCatChem 6, no. 6 (2014): 1679–83. http://dx.doi.org/10.1002/cctc.201400014.

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

Wang, Yahui, Paul R. McGonigal, Bart Herlé, Maria Besora, and Antonio M. Echavarren. "Gold(I) Carbenes by Retro-Buchner Reaction: Generation and Fate." Journal of the American Chemical Society 136, no. 2 (2013): 801–9. http://dx.doi.org/10.1021/ja411626v.

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

Moody, Christopher J., Soyfur Miah, Alexandra M. Z. Slawin, Darren J. Mansfield, and Ian C. Richards. "Stereocontrol in the intramolecular Buchner reaction of diazoamides and diazoesters." Journal of the Chemical Society, Perkin Transactions 1, no. 24 (1998): 4067–76. http://dx.doi.org/10.1039/a807622g.

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

Dissertations / Theses on the topic "Buchner reaction"

1

Herlé, Bart. "Stereoselective Cyclopropanations via Gold(I)-Catalyzed Retro-Buchner Reactions." Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/454770.

Full text
Abstract:
La formació de carbens bencílics d’or(I) a partir de cicloheptatriens substituïts en la posició 7, a través de la reacció de retro-Buchner, ha aparegut recentment com una alternativa segura i versàtil a la descomposició de diazocompostos. No obstant, la formació de dits carbens requereix altes temperatures, limitant la seva aplicació. El treball d’aquest tesi doctoral s’ha dedicat a superar aquesta desavantatge i millorar la versatilitat de la transformació. Els derivats de 1H-ciclopropa[l]fenantrè, que s’assemblen al tautòmer norcaradiè del cicloheptatriè, es descomponen per donar lloc a
APA, Harvard, Vancouver, ISO, and other styles
2

Phung, Bich Tuyen. "Etude de la sélectivité dans la réaction de Buchner." Electronic Thesis or Diss., Université Grenoble Alpes, 2024. https://theses.hal.science/tel-04651531.

Full text
Abstract:
Le travail présenté dans ce manuscrit est divisé en deux grandes parties. Dans un premier temps, une étude sera présentée sur des problème de chimiosélectivité observés lors de la réaction de transfert de carbène. Des composés diazo différemment substitués ont été généré comme précurseur de carbène, et la réaction de transfert de carbène a été effectuée en présence de Rh2(OAc)4. Les résultats montrent une compétition entre la réaction de Buchner et l’insertion C‒H en position benzylique, dépendant de la substituant du diazo. Des calculs de DFT ont ensuite été réalisés pour compléter les inform
APA, Harvard, Vancouver, ISO, and other styles
3

Yin, Xiang. "Synthesis of Indenes and Indanes by Gold(I)-Catalyzed Decarbenation." Doctoral thesis, Universitat Rovira i Virgili, 2018. http://hdl.handle.net/10803/665105.

Full text
Abstract:
Els derivats de 7-substituts de 1,3,5-cicloheptatrienes reaccionen amb catalitzadors d'or (I) catiònic que donen carbens d'or (I) per una reacció retro-Buchner en què dos enllaços C-C en Norcaradienes són trencats per Au (I). Aquesta nova estratègia obvia l'ús de derivats diazo sensibles a xocs i genera carbens metàl·lics reactius in situ que poden experimentar diverses transformacions més, com ara la ciclopropanació d'alquens externs i reticulats i les reaccions tipus Friedel-Crafts intramoleculars. Per ampliar la gamma de mètodes sintètics i aplicacions disponibles per a aquests intermedis ú
APA, Harvard, Vancouver, ISO, and other styles
4

Schmidt, Renato Jose. "Development of a real-time quantitative polymerase chain reaction method to quantify Lactobacillus buchneri in order to study its growth and effects in silages when added alone or in combination with Pediococcus pentosaceus." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 169 p, 2008. http://proquest.umi.com/pqdweb?did=1601513951&sid=1&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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

Buchert, Felix Eberhard [Verfasser]. "The chloroplast ATP synthase upon oxidative stress : critical targets of reactive oxygen species / Felix Eberhard Buchert." Gießen : Universitätsbibliothek, 2012. http://d-nb.info/1064173403/34.

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

Nani, Roger Rauhauser. "The Intramolecular Buchner Reaction of α-Diazo-β-Ketonitriles: Development and Application to the Total Synthesis of (+)-Salvileucalin B". Thesis, 2013. https://thesis.library.caltech.edu/7847/1/Nani-R-R-2013thesis.pdf.

Full text
Abstract:
<p>Since its discovery in 1896, the Buchner reaction has fascinated chemists for more than a century. The highly reactive nature of the carbene intermediates allows for facile dearomatization of stable aromatic rings, and provides access to a diverse array of cyclopropane and seven-membered ring architectures. The power inherent in this transformation has been exploited in the context of a natural product total synthesis and methodology studies.</p> <p>The total synthesis work details efforts employed in the enantioselective total synthesis of (+)-salvileucalin B. The fully-substituted cy
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Buchner reaction"

1

Li, Jie Jack. "Buchner-Curtius-Schlotterbeck reaction." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_47.

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

Li, Jie Jack. "Buchner-Curtius-Schlotterbeck reaction." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_45.

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

Li, Jie Jack. "Bucherer reaction." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_45.

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

Li, Jie Jack. "Bucherer reaction." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_42.

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

Li, Jie Jack. "Bucherer reaction." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_43.

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

Li, Jie Jack. "Bucherer reaction." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_37.

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

Li, Jie Jack. "Buchner method of ring expansion." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_48.

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

Li, Jie Jack. "Buchner method of ring expansion." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_46.

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

Li, Jie Jack. "Bucherer-Bergs reaction." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_46.

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

Li, Jie Jack. "Bucherer–Bergs reaction." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_43.

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

Conference papers on the topic "Buchner reaction"

1

Krunić, Mihajlo J., Jelena Z. Penjišević, Slađana Kostić-Rajačić, Vladimir B. Šukalović, Deana B. Andrić, and Ivana I. Jevtić. "Pyrazole/tacrine derivatives as potential cholinesterase inhibitors." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.567k.

Full text
Abstract:
Two new tacrine/pyrazole conjugates were designed, synthesized, and pharmacologically evaluated for their inhibitory activity toward acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). A scalable and cost-efficient synthetic route was developed, and key reaction steps for the synthesis of compounds 4a,b were nucleophilic substitution of α-aroylketene dithioacetals with tacrine intermediates, followed by cyclocondensation of respective N,S-acetals with hydrazine hydrate. The preliminary pharmacological evaluation revealed high inhibitory activities of 4a,b toward AChE (180 and 259 nM
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Buchner reaction' 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