Relevant bibliographies by topics / Rearrangements (Chemistry) Carbinyl compounds

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

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

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Rearrangements (Chemistry) Carbinyl compounds"

1

Baldwin, John E., Samuel Bonacorsi, Robert G. Carlson, and Forest D. Graber. "Cyclohexyl(2-methylenecyclopropyl)carbinyl carbocationic rearrangements." Journal of Organic Chemistry 58, no. 4 (1993): 981–84. http://dx.doi.org/10.1021/jo00056a042.

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Tanko, James M., and Ray E. Drumright. "Radical ion probes. I. Cyclopropyl-carbinyl rearrangements of aryl cyclopropyl ketyl anions." Journal of the American Chemical Society 112, no. 13 (1990): 5362–63. http://dx.doi.org/10.1021/ja00169a060.

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Ranu, Brindaban C., Subhash Banerjee, and Arijit Das. "Catalysis by ionic liquids: cyclopropyl carbinyl rearrangements catalyzed by [pmim]Br under organic solvent free conditions." Tetrahedron Letters 47, no. 6 (2006): 881–84. http://dx.doi.org/10.1016/j.tetlet.2005.12.003.

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Vos, Johannes G., and Mary T. Pryce. "Photoinduced rearrangements in transition metal compounds." Coordination Chemistry Reviews 254, no. 21-22 (2010): 2519–32. http://dx.doi.org/10.1016/j.ccr.2010.04.010.

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Kolodiazhnyi, Oleg I., Evgen Grishkun, Oleg Golovatyi, and Sergei Ustenko. "Diastereoselective Rearrangements and Epimerization of Organophosphorus Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 109, no. 1-4 (1996): 485–88. http://dx.doi.org/10.1080/10426509608545196.

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6

Beck, Karin, Harald Burghard, Gabriele Fischer, Siegfried Hünig, and Petra Reinold. "Azo Cope Rearrangements of Nonstabilized Azo Compounds." Angewandte Chemie International Edition in English 26, no. 7 (1987): 672–73. http://dx.doi.org/10.1002/anie.198706721.

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7

Lerman, Berta M. "Skeletal rearrangements of cage compounds with medium rings." Russian Chemical Reviews 60, no. 4 (1991): 358–72. http://dx.doi.org/10.1070/rc1991v060n04abeh001082.

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Fañanás, Francisco J., Mónica Álvarez-Pérez, and Félix Rodríguez. "IPy2BF4-Mediated Rearrangements of 1,2-Difunctionalized Compounds and Olefins." Chemistry - A European Journal 11, no. 20 (2005): 5938–44. http://dx.doi.org/10.1002/chem.200500070.

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Magnusson, Göran. "REARRANGEMENTS OF EPOXY ALCOHOLS AND RELATED COMPOUNDS. A REVIEW." Organic Preparations and Procedures International 22, no. 5 (1990): 547–74. http://dx.doi.org/10.1080/00304949009356326.

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10

Scott, Lawrence T., Nicolas H. Roelofs, and Tsze Hong Tsang. "Thermal rearrangements of aromatic compounds. 10. Automerization of benzene." Journal of the American Chemical Society 109, no. 18 (1987): 5456–61. http://dx.doi.org/10.1021/ja00252a024.

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

1

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/.

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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
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2

Rigby, Suzie S. "Sigmatropic and haptotropic shifts in complexes of cyclopenta(l)phenanthrene." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape16/PQDD_0020/NQ30185.pdf.

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Suvannachut, Kessara. "Scope and mechanism of the rearrangement of alkoxybenzyl anions to alkylphenoxide ions; cyclophanes from 2,6-dimethylanisole." Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184679.

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Alkoxy alkyl groups migrate to benzylic carbon when alkyl alkylphenyl ethers are treated with n-butyllithium and potassium t-butoxide. For alkyl 2,6-dialkylphenyl ethers, yields of the rearrangement products range from 45-70%. Rearrangement products are obtained in 10-30% yield from other dimethylanisoles and methylanisoles. The reactions appear to proceed by homolytic cleavage of the alkoxy alkyl group of alkoxybenzyl anions followed by recombination of the resulting radical pair in a different way. The reaction is useful for preparing 2,6-dialkylphenols and their corresponding ethers. The re
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4

Liu, Gu. "Target identification and validation studies in chemical biology & Synthesis of medium-sized ring containing compounds via oxidative fragmentation." Thesis, University of St Andrews, 2010. http://hdl.handle.net/10023/986.

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Part I of this thesis describes the development of bioactive small molecules of relevance to the study of the apicomlexan parasite Toxoplasma gondii into useful chemical tools. The research includes the target identification and validation studies, using both chemical and biological methods. Chapter 1 provides an overview of chemical genetics with a particular emphasis on methods for the identification of the protein targets of bioactive small molecules. The concept of biochemical protein target identification techniques was introduced with a detailed discussion of interesting applications fro
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5

Campbell, Craig D. "Lewis base-promoted organocatalysis : O- to C-carboxyl transfer reactions." Thesis, University of St Andrews, 2010. http://hdl.handle.net/10023/2609.

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This work describes the application of a variety of Lewis bases, encompassing predominantly N-heterocyclic carbenes (NHCs), but also the use of imidazoles, aminopyridines, amidines and isothioureas, as effective catalysts in the dearomatisation of heterocyclic carbonates, predominantly the rearrangement of oxazolyl carbonates to their C-carboxyazlactone isomers by means of the Steglich rearrangement. This rearrangement reaction has been investigated extensively, with the development of simplified reaction procedures and the invention of domino cascade protocols incorporating this transformatio
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6

Kinal, Armagan. "Theoretical Investigation Of Unimolecular Reactions Of Cyclic C5h6 Compounds By Ab Initio Quantum Chemical Methods." Phd thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605124/index.pdf.

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Thermodynamic stabilities of eighteen cyclic C5H6 isomers were explored computationally both on singlet and triplet state potential energy surfaces (PES). All isomers have singlet ground states except for bicyclo[2.1.0]pent-5-ylidene (B5) having no stable geometry on the singlet C5H6 PES. Cyclopenta-1,3-diene (M1) is the most stable cyclic C5H6 isomer while cyclopent-1,4-diylidene is the least stable one among all. Cyclopenta-1,2-diene (M2) and cyclopentyne (M3) have biradical characters of 46.9 and 21.5%, respectively. Seven unimolecular isomerization reactions occurring among several of the
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7

Wang, Jin. "Ultrafast studies of reactive intermediates." Columbus, Ohio : Ohio State University, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1196155202.

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Hattingh, Johannes Theobaldus Zacharias. "Sintonsinteses van gekoördineerde tione en tiokarbene." Thesis, 2015. http://hdl.handle.net/10210/14759.

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Books on the topic "Rearrangements (Chemistry) Carbinyl compounds"

1

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

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2

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

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

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4

Rojas, Christian M. Molecular Rearrangements in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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5

Rojas, Christian M. Molecular Rearrangements in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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Rojas, Christian M. Molecular Rearrangements in Organic Synthesis. Wiley & Sons, Incorporated, John, 2015.

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7

Deshayes, Kurt D. Studies of spiro[pyranindoline] compounds and their application to photodynamic transport. 1988.

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8

Conti, Nicholas Joseph. Thermal and photo-induced rearrangements of sigma-bound cyclopropyl iron complexes: Synthesis of a novel metallacyclic iron dicarbene complex. 1987.

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9

Phanstiel, Otto. The effect of a single fluorine substituent on the [1,5] homodienyl hydrogen shift, the solvolytic ring-opening of bromocyclopropane, and the [1,3] carbon shift of 6-methylenebicyclo[3.2.0]hept-2-ene. 1988.

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

1

Reggelin, Michael. "[2,3]-Sigmatropic Rearrangements of Allylic Sulfur Compounds." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/128_2006_103.

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Quirós, María Teresa, and María Paz Muñoz. "Synthesis of Heterocyclic Compounds via Gold-Catalysed Enyne Rearrangements." In Topics in Heterocyclic Chemistry. Springer International Publishing, 2015. http://dx.doi.org/10.1007/7081_2015_5004.

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3

"MOLECULAR REARRANGEMENTS OF COORDINATION COMPOUNDS." In Synthetic Coordination Chemistry: Principles and Practice. WORLD SCIENTIFIC, 1996. http://dx.doi.org/10.1142/9789812831378_0011.

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4

Pace, Andrea, Silvestre Buscemi, Ivana Pibiri, Nicolò Vivona, and Domenico Spinelli. "Heterocyclic Rearrangements: An Expedient Route to the Synthesis of Fluorinated Heterocyclic Compounds‡‡Financial support through the Italian MIUR and University of Palermo within the National Research Project “Fluorinated Compounds: New Materials for Advanced Applications”." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50269-0.

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