Relevant bibliographies by topics / Rearrangements (Chemistry) Chemistry

Contents

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

Academic literature on the topic 'Rearrangements (Chemistry) Chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 3 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 'Rearrangements (Chemistry) Chemistry.'

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 "Rearrangements (Chemistry) Chemistry"

1

Debnath, Pradip. "Recent Advances in the Synthesis of Amides via Oxime Rearrangements and its Applications." Current Organic Synthesis 15, no. 5 (2018): 666–706. http://dx.doi.org/10.2174/1570179415666180416151039.

Full text
Abstract:
Background: Amide bond formation reactions are the most important transformations in (bio)organic chemistry because of the widespread occurrence of amides in pharmaceuticals, natural products and biologically active compounds. The Beckmann rearrangement is a well-known method used for the preparation of secondary amides from ketoximes. But, most of the traditional protocols used for the Beckmann rearrangement create enormous amount of wastes. Thus, the atom economical synthesis of amides has got high priority among the chemists. However, under classical Beckmann conditions, aldoximes do not re
APA, Harvard, Vancouver, ISO, and other styles
2

Yaremenko, Ivan A., Vera A. Vil’, Dmitry V. Demchuk, and Alexander O. Terent’ev. "Rearrangements of organic peroxides and related processes." Beilstein Journal of Organic Chemistry 12 (August 3, 2016): 1647–748. http://dx.doi.org/10.3762/bjoc.12.162.

Full text
Abstract:
This review is the first to collate and summarize main data on named and unnamed rearrangement reactions of peroxides. It should be noted, that in the chemistry of peroxides two types of processes are considered under the term rearrangements. These are conventional rearrangements occurring with the retention of the molecular weight and transformations of one of the peroxide moieties after O–O-bond cleavage. Detailed information about the Baeyer−Villiger, Criegee, Hock, Kornblum−DeLaMare, Dakin, Elbs, Schenck, Smith, Wieland, and Story reactions is given. Unnamed rearrangements of organic perox
APA, Harvard, Vancouver, ISO, and other styles
3

Lefebvre, Corentin, Lucas Fortier, and Norbert Hoffmann. "Photochemical Rearrangements in Heterocyclic Chemistry." European Journal of Organic Chemistry 2020, no. 10 (2019): 1393–404. http://dx.doi.org/10.1002/ejoc.201901190.

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

Kapovits, István, József Rábai, Dénes Szabó та Miklós Kuti. "Rearrangements in Spiro-λ4-sulfane Chemistry". Phosphorus, Sulfur, and Silicon and the Related Elements 120, № 1 (1997): 435–36. http://dx.doi.org/10.1080/10426509708545585.

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

Hanson, James R. "Aphidicolin: Its Chemistry and Biosynthesis." Journal of Chemical Research 42, no. 8 (2018): 395–401. http://dx.doi.org/10.3184/174751918x15333061990467.

Full text
Abstract:
1. Introduction 2. Naturally occurring aphidicolanes 3. The chemistry of aphidicolin 4. Synthesis 5. Biosynthesis 6. References The occurrence and structure of the biologically active tetracyclic diterpenoid aphidicolin and related aphidicolane natural products, together with their chemistry, their molecular rearrangements and their biosynthesis, are reviewed.
APA, Harvard, Vancouver, ISO, and other styles
6

Werschkun, Barbara, and Joachim Thiem. "ChemInform Abstract: Claisen Rearrangements in Carbohydrate Chemistry." ChemInform 32, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.200151270.

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

GRIDNEV, I. "Sigmatropic and haptotropic rearrangements in organometallic chemistry." Coordination Chemistry Reviews 252, no. 15-17 (2008): 1798–818. http://dx.doi.org/10.1016/j.ccr.2007.10.021.

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

Hanson, James R. "Stereochemical Aspects of Some Rearrangements of Gibberellic Acid." Journal of Chemical Research 42, no. 6 (2018): 285–90. http://dx.doi.org/10.3184/174751918x15294211268538.

Full text
Abstract:
The stereochemistry of some rearrangement reactions of the diterpenoid plant hormone gibberellic acid, including the allylic rearrangements of substituents and the lactone in ring A, rearrangements involving ring B and the Wagner–Meerwein rearrangements of rings C and D, are reviewed.
APA, Harvard, Vancouver, ISO, and other styles
9

Klumpp, Douglas A. "Molecular rearrangements of superelectrophiles." Beilstein Journal of Organic Chemistry 7 (March 23, 2011): 346–63. http://dx.doi.org/10.3762/bjoc.7.45.

Full text
Abstract:
Superelectrophiles are multiply charged cationic species (dications, trications, etc.) which are characterized by their reactions with weak nucleophiles. These reactive intermediates may also undergo a wide variety of rearrangement-type reactions. Superelectrophilic rearrangements are often driven by charge–charge repulsive effects, as these densely charged ions react so as to maximize the distances between charge centers. These rearrangements involve reaction steps similar to monocationic rearrangements, such as alkyl group shifts, Wagner–Meerwein shifts, hydride shifts, ring opening reaction
APA, Harvard, Vancouver, ISO, and other styles
10

Kimura, Tsutomu. "Recent Advances in Magnesium Carbenoid Chemistry." Synthesis 49, no. 23 (2017): 5105–19. http://dx.doi.org/10.1055/s-0036-1590894.

Full text
Abstract:
Magnesium carbenoids are a class of organomagnesium species possessing a halo group at the α-position. The reactions of magnesium carbenoids can be classified into the following three categories: nucleophilic reactions resembling Grignard reagents, electrophilic reactions resembling organic halides, and rearrangements resembling carbenes. This short review summarizes recent studies on magnesium carbenoids reported between 2010 and 2016, and milestone studies reported before 2010 according to the classification of the reactions into the aforementioned three categories.1 Introduction2 Structures
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Rearrangements (Chemistry) Chemistry"

1

Sellers, Thomas G. R. "Stereoselective N,O rearrangements." Thesis, University of Oxford, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270280.

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

Mohamed, Mustafa Abdi. "Synthesis of [alpha]-allynyl and [alpha]-allylsilane amino acids by the Claisen rearrangement /." *McMaster only, 2001.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Guevel, Ronan. "Synthetic Studies towards Vinigrol Tandem Cope-Cope Rearrangements /." The Ohio State University, 1994. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487850665559446.

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

Birkinshaw, Simon Jonathan. "1,2-metallate rearrangements of #alpha#-alkoxyvinylborates." Thesis, University of Southampton, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293210.

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

Mohamed, Mubina. "Understanding cyclobutenone rearrangements : a study under flow." Thesis, University of Southampton, 2014. https://eprints.soton.ac.uk/362639/.

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

McCormick, Alison Sarah. "Synthesis and rearrangements of vinylidenecyclopropanes and dimethylenecyclopropanes." Thesis, University of Edinburgh, 1985. http://hdl.handle.net/1842/15322.

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

Loparo, Joseph J. (Joseph John). "Ultrafast structural fluctuations and rearrangements of water's hydrogen bonded network." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/38623.

Full text
Abstract:
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, February 2007.<br>"December 2006." Vita.<br>Includes bibliographical references.<br>Aqueous chemistry is strongly influenced by water's ability to form an extended network of hydrogen bonds. It is the fluctuations and rearrangements of this network that stabilize reaction products and drive the transport of excess protons through solution. Experimental observations of the dynamics of the hydrogen bonded network are difficult because (1) the timescales are exceedingly fast with relevant fluctuations occurring on a tens
APA, Harvard, Vancouver, ISO, and other styles
8

Mulhall, Steven Eric. "I. Rearrangements of beta-heteroatomic carbenes ; II. Chemistry of 2-tert-butyl-4-diazobenzopyran /." The Ohio State University, 1989. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487675687173776.

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

Gabbutt, Christopher David. "Reactions and rearrangements of chroman-4-ones and related compounds." Thesis, University of Central Lancashire, 1987. http://clok.uclan.ac.uk/19780/.

Full text
Abstract:
The synthesis of a range of novel 2,2-disubstituted chroman-4-ones has been accomplished by the pyrrolidine catalysed condensation of a 2-hydroxyacetophenone with aldehydes and ketones. The reaction permits access to both symmetrically and unsymmetrically substituted compounds. The reaction has been extended to the preparation of a novel furochromanone, an analogue of the natural product khellin. The Schmidt reaction of 2,2-disubstituted chroman-4-ones in an acetic-sulphuric acid mixture affords 2,3,4.5-tetrahydro-1.4- benzoxazepine-5(411)--ones, resulting from alkyl migration of the iminodisz
APA, Harvard, Vancouver, ISO, and other styles
10

老永康 and Wing-hong Lo. "Novel rearrangements of dioxodibenz[b,f]azocine." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1996. http://hub.hku.hk/bib/B3121437X.

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

Books on the topic "Rearrangements (Chemistry) Chemistry"

1

Polar rearrangements. Oxford University Press, 1992.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Patel, Sunita Thakordas. Sigmatropic rearrangements in organofluorine chemistry. University of Birmingham, 1994.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Plath, Peter Jörg. Diskrete Physik molekularer Umlagerungen. Teubner, 1988.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Molecular rearrangements in organic synthesis. John Wiley & Sons, Inc., 2015.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Lin, Zhi-Ping. Some applications of ultrasound irradiation in pinacol coupling of carbonyl compounds. Nova Science Publishers, 2010.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Baer, Tomas. Unimolecular reaction dynamics: Theory and experiments. Oxford University Press, 1996.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Anisimov, A. V. Molekuli͡a︡rnye peregruppirovki seroorganicheskikh soedineniĭ: Organicheskie sulʹfidy. Izd-vo Moskovskogo universiteta, 1989.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Witczak, Zbigniew J., and Roman Bielski. Domino and intramolecular rearrangement reactions as advanced synthetic methods in glycoscience. John Wiley & Sons Inc., 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Photoisomerization: Causes, Behavior and Effects. Nova Science Publishers, Incorporated, 2019.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Daruwala, Khushroo Peshotan. Substituent control in the oxy-Cope rearrangements of 1-vinyl-trans-cyclotridec-3-en-1-ol systems. 1986.

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

Book chapters on the topic "Rearrangements (Chemistry) Chemistry"

1

Ripin, David H. B. "Rearrangements." In Practical Synthetic Organic Chemistry. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118093559.ch7.

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

Dinda, Biswanath. "Sigmatropic Rearrangements." In Lecture Notes in Chemistry. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-45934-9_4.

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

Wirth, Thomas. "Oxidations and Rearrangements." In Hypervalent Iodine Chemistry. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_7.

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

Werschkun, Barbara, and Joachim Thiem. "Claisen Rearrangements in Carbohydrate Chemistry." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/3-540-44422-x_11.

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

Maertens, Gaëtan, and Sylvain Canesi. "Rearrangements Induced by Hypervalent Iodine." In Hypervalent Iodine Chemistry. Springer International Publishing, 2015. http://dx.doi.org/10.1007/128_2015_657.

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

Carey, Francis A., and Richard J. Sundberg. "Cycloadditions, Unimolecular Rearrangements, and Thermal Eliminations." In Advanced Organic Chemistry. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-9797-7_6.

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

de la Pradilla, Roberto Fernández, Mariola Tortosa, and Alma Viso. "Sulfur Participation in [3,3]-Sigmatropic Rearrangements." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/128_059.

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

Snape, Timothy J. "Aromatic Rearrangements in Which the Migrating Group Migrates to the Aromatic Nucleus." In Arene Chemistry. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118754887.ch18.

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

Osanai, S. "Nickel(II)-Catalyzed Rearrangements of Free Sugars." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/3-540-44422-x_4.

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

Lundt, Inge, and Robert Madsen. "Synthetically Useful Base-Induced Rearrangements of Aldonolactones." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/3-540-44422-x_8.

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

Conference papers on the topic "Rearrangements (Chemistry) Chemistry"

1

Hessler, Filip, and Martin Kotora. "Synthesis and rearrangements of Dewar benzene deoxyribosides." In XVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112334.

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

Mues, H., and U. Kazmaier. "Via Ester Enolate Claisen Rearrangements To a Variety of Non-Proteinogenic Amino Acids." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01901.

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

Ungur, Nicon, and Veaceslav Kulcitki. "Mollecular rearrangements in the synthesis of bioactive terpenoids with new carbon skeletons." In New frontiers in natural product chemistry, scientific seminar with international participation. Institute of Chemistry, 2021. http://dx.doi.org/10.19261/nfnpc.2021.ab11.

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

Bouyer, Frédéric, and Gérard Picard. "Evidence of cations’ influence for structural rearrangements in cryolitic melts." In The 54th international meeting of physical chemistry: Fast elementary processes in chemical and biological systems. AIP, 1996. http://dx.doi.org/10.1063/1.50142.

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

Hassan, Mohamed, Hanan Salah, and Eman Abdalla. "Ring Rearrangements and Reactivity of 3-((4-oxo-4H-chromen-3-yl)methylene)-4-phenyl-1H-[1,5]benzodiazepin-2(3H)-one Towards Some Nucleophiles." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a046.

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

Bilokin, Yaroslav, Sergey Kovalenko, Maxim Vasilyef, Igor Bylov, and Konstantin Sytnik. "2-Imino-2H-1-benzopyrans as Versatile Synthons in Heterocyclic Synthesis: Studies on Novel Rearrangements of 3-Substituted 2-Imino-2H-1- benzopyrans Under Action of N-Nucleophiles." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01676.

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

Marín-Luna, M., M. Alajarín, M. M. Ortín, P. Sánchez-Andrada, and A. Vidal. "Benzylic Newman-Kwart rearrangement triggered by Phosphanes." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01203.

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

Schnell, Barbara, and Thomas Kappe. "Rearrangement of Heterocycles via-2-oxoketenes: Synthesis and Rearrangement Reactions of Cross-Conjugated Mesomeric Pyridazino[2,3-a]pyrimidine." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01844.

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

Allin, Steven, Rob Baird, and Martin Button. "Synthetic Applications of the Asymmetric Amino-Cope Rearrangement." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01797.

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

Seijas, Julio, M. Vàsquez-Tato, and Luis Barreiro-Castro. "Reactivity of styrene derivatives: Nucleophilic addition versus 1,2-wittig rearrangement." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01670.

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