Relevant bibliographies by topics / Corey-Kim oxidation

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Academic literature on the topic 'Corey-Kim oxidation'

Author: Grafiati
Published: 5 June 2025
Last updated: 15 July 2025

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Journal articles on the topic "Corey-Kim oxidation"

1

Ramadas, Chavakula, Rao Mutyala Narayana, and Rao Chennupati Srinivasa. "Industrially viable synthesis of 3-[3-(trifluoromethyl)phenyl]propionaldehyde. A key intermediate of cinacalcet." Journal of Indian Chemical Society Vol. 90, Aug 2013 (2013): 1259–61. https://doi.org/10.5281/zenodo.5788361.

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Tyche Industries Limited, H. No. C-21/A, Road No. 9, Film Nagar, Jubilee Hills, Hyderabad-500 093, India <em>E-mail </em>: das.krishnac@gmail.com <em>Manuscript received online 15 June 2012, accepted 29 September 2012</em> An improved synthesis of 3-[3-(trifluoromethyl)phenyl]propionaldehyde (2), a key intermediate of cinacalcet hydrochloride ((<em>R</em>)-alpha-methyl-<em>N</em>-[3-[3-(triflouoromethyl)phenyl]propyl]-1-naphthalene methane amine hydrochloride) has been described. The key step include the Corey-Kim oxidation under normal conditions.
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2

Tsuchiya, Daisuke, Masayuki Tabata, Katsuhiko Moriyama, and Hideo Togo. "Efficient Swern oxidation and Corey–Kim oxidation with ion-supported methyl sulfoxides and methyl sulfides." Tetrahedron 68, no. 34 (2012): 6849–55. http://dx.doi.org/10.1016/j.tet.2012.06.026.

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Tsuchiya, Daisuke, Masayuki Tabata, Katsuhiko Moriyama, and Hideo Togo. "ChemInform Abstract: Efficient Swern Oxidation and Corey-Kim Oxidation with Ion-Supported Methyl Sulfoxides and Methyl Sulfides." ChemInform 44, no. 1 (2013): no. http://dx.doi.org/10.1002/chin.201301036.

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4

Ramadas, Chavakula, Reddy Karuru Mallikarjuna, Saladi J. S. Chakradhar, Gouri K. Vijaya, N. Annapurna, and Babu K. Raghu. "An improved and green synthesis of N-benzyl-4-formylpiperidine, a key intermediate of donepezil." Journal of Indian Chemical Society Vol. 95, Oct 2018 (2018): 1245–48. https://doi.org/10.5281/zenodo.5653511.

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Research and Development, Aurobindo Pharma Limited, Survey No: 71 &amp; 72, Indrakaran Village, Sangareddy Mandal, Medak-502 329, Telangna, India E-mail: ramadas.chavakula@gmail.com Department of Engg. Chemistry, Andhra University, Visakhapatnam-530 003, Andhra Pradesh, India <em>Manuscript received 08 June 2018, accepted 14 August 2018</em> An industrially viable and green synthesis of <em>N</em>-benzyl-4-formylpiperdine (<strong>2</strong>), a key intermediate of <em>Donepezil hydrochloride </em>(<strong>3</strong>) (Aricept<sup>&reg;</sup>), a selective inhibitor of acetyl cholinesterase (A
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5

Katayama, Sadamu, Kinue Fukuda, Toshio Watanabe, and Masashige Yamauchi. "Synthesis of 1,3-Dicarbonyl Compounds by the Oxidation of 3-Hydroxycarbonyl Compounds with Corey-Kim Reagent." Synthesis 1988, no. 03 (1988): 178–83. http://dx.doi.org/10.1055/s-1988-27506.

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6

Nishide, Kiyoharu, Pranab K. Patra, Manabu Matoba, Kandasamy Shanmugasundaram, and Manabu Node. "A practical improvement of odorless Corey–Kim and Swern oxidations." Green Chem. 6, no. 3 (2004): 142–46. http://dx.doi.org/10.1039/b312849k.

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7

Nishide, Kiyoharu, Shin-ichi Ohsugi, Masato Fudesaka, Sumiaki Kodama, and Manabu Node. "New odorless protocols for the Swern and Corey–Kim oxidations." Tetrahedron Letters 43, no. 29 (2002): 5177–79. http://dx.doi.org/10.1016/s0040-4039(02)00968-1.

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Nishide, Kiyoharu, Shin-ichi Ohsugi, Masato Fudesaka, Sumiaki Kodama, and Manabu Node. "ChemInform Abstract: New Odorless Protocols for the Swern and Corey-Kim Oxidations." ChemInform 33, no. 43 (2010): no. http://dx.doi.org/10.1002/chin.200243057.

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Ohsugi, Shin-ichi, Kiyoharu Nishide, Keiji Oono, et al. "New odorless method for the Corey–Kim and Swern oxidations utilizing dodecyl methyl sulfide (Dod-S-Me)." Tetrahedron 59, no. 42 (2003): 8393–98. http://dx.doi.org/10.1016/j.tet.2003.08.055.

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10

Iula, Donna M. "ChemInform Abstract: Corey-Kim Oxidation." ChemInform 39, no. 37 (2008). http://dx.doi.org/10.1002/chin.200837235.

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Book chapters on the topic "Corey-Kim oxidation"

1

Li, Jie Jack. "Corey-Kim oxidation." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_72.

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Li, Jie Jack. "Corey–Kim oxidation." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_72.

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Li, Jie Jack. "Corey-Kim oxidation." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_67.

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4

Li, Jie Jack. "Corey–Kim oxidation." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_65.

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5

Taber, Douglass F. "New Methods for Carbocyclic Construction: The Kim Synthesis of Pentalenene." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0080.

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Daesung Lee of the University of Illinois, Chicago, taking advantage of the facile insertion of an alkylidene carbene into a C-Si bond, established (J. Am. Chem. Soc. 2010, 132, 6640) a general method for the conversion of an α-silyl ketone 1 into the silyl cyclopropene 3. Christopher D. Bray of Queen Mary University showed (J. Org. Chem. 2010, 75, 4652) that the sulfonyl phosphonate 5 converted the enantiomerically pure epoxide 4 into the cyclopropane 6. Paul Margaretha of the University of Hamburg observed (Organic Lett. 2010, 12, 728) smooth photochemical combination of 7 and 8 to give 9 with high diastereocontrol. Tõnis Kanger of the Tallinn University of Technology devised (Organic Lett. 2010, 12, 2230) the three-component coupling of 10, 11, and diethyl amine to give, after reduction, the highly substituted cyclobutane 12. Min Shi of the Shanghai Institute of Organic Chemistry uncovered (J. Org. Chem. 2010, 75, 902) an interesting new thermal rearrangement: the conversion of 13 to 14. José G. Ávila-Zárraga of the Universidad Nacional Autónoma de México applied (Tetrahedron Lett. 2010, 51, 2232) Pd catalysis to the cyclization of the epoxy nitrile 15, redirecting the reaction from the expected cyclobutane to the cyclopentanol 16. Ullrich Jahn of the Academy of Sciences of the Czech Republic effected (J. Org. Chem. 2010, 75, 4480) the oxidative radical cyclization of 17 to 18. Initial deprotonation of the substrate with t -BuMgCl switched the product to the trans diastereomer. Jonathan W. Burton of the University of Oxford employed (Organic Lett. 2010, 12, 2738) a related oxidative cyclization for the diastereoselective conversion of 19 to 20. E. J. Corey of Harvard University reported (Organic Lett. 2010, 12, 300) a new ligand for the enantioselective Ni-mediated reduction of 21 to 22. Shu-Li You, also of the Shanghai Institute of Organic Chemistry, established (J. Am. Chem. Soc. 2010, 132, 4056) that the alcohol 23, readily prepared by oxidation of p -cresol, could be cyclized to the crystalline 25 in high ee.
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