Relevant bibliographies by topics / Ritter amidation

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  1. Journal articles

Academic literature on the topic 'Ritter amidation'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Ritter amidation"

1

Chai, Jinkui, Wei Ding, Chen Wang, Shingo Ito, Junliang Wu, and Naohiko Yoshikai. "Ritter-type iodo(iii)amidation of unactivated alkynes for the stereoselective synthesis of multisubstituted enamides." Chemical Science 12, no. 45 (2021): 15128–33. http://dx.doi.org/10.1039/d1sc05240c.

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2

Cazorla, Clément, Estelle Métay, Bruno Andrioletti, and Marc Lemaire. "Ritter-type amidation of alkylboron derivatives with nitriles." Tetrahedron Letters 50, no. 49 (2009): 6855–57. http://dx.doi.org/10.1016/j.tetlet.2009.09.132.

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3

Khusnutdinov, Ravil I., Tatyana M. Egorova, Ekaterina S. Meshcheryakova, Leonard M. Khalilov, and Usein M. Dzhemilev. "The ferric chloride-catalyzed Ritter amidation of norbornane-type dienes." Mendeleev Communications 29, no. 2 (2019): 143–44. http://dx.doi.org/10.1016/j.mencom.2019.03.007.

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4

Cazorla, Clement, Estelle Metay, Bruno Andrioletti, and Marc Lemaire. "ChemInform Abstract: Ritter-Type Amidation of Alkylboron Derivatives with Nitriles." ChemInform 41, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.201011049.

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5

Firouzabadi, H., A. R. Sardarian, and H. Badparva. "Highly Selective Amidation of Benzylic Alcohols with Nitriles. A Modified Ritter Reaction." Synthetic Communications 24, no. 5 (1994): 601–7. http://dx.doi.org/10.1080/00397919408012637.

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6

Khusnutdinov, Ravil I., Tatyana M. Egorova, Rishat I. Aminov, Ekaterina S. Mescheryakova, and Leonard M. Khalilov. "Iron(III) chloride promoted Ritter amidation of saturated cyclopropane-containing polycyclic hydrocarbons." Mendeleev Communications 30, no. 3 (2020): 369–71. http://dx.doi.org/10.1016/j.mencom.2020.05.036.

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7

Park, Sang Won, Soong-Hyun Kim, Jaeyoung Song, et al. "Hypervalent iodine-mediated Ritter-type amidation of terminal alkenes: The synthesis of isoxazoline and pyrazoline cores." Beilstein Journal of Organic Chemistry 14 (May 11, 2018): 1028–33. http://dx.doi.org/10.3762/bjoc.14.89.

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Hypervalent iodine-mediated olefin functionalization provides a rapid gateway towards accessing both various heterocyclic cores and functional groups. In this regard, we have developed a Ritter-type alkene functionalization utilizing a PhI(OAc)2 ((diacetoxyiodo)benzene, PIDA)/Lewis acid combination in order to access isoxazoline and pyrazoline cores. Based on allyl ketone oximes and allyl ketone tosylhydrazones, we have developed an alkene oxyamidation and amido-amidation protocol en route to accessing both isoxazoline and pyrazoline cores. Additionally, acetonitrile serves as both the solvent
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8

FIROUZABADI, H., A. R. SARDARIAN, and H. BADPARVA. "ChemInform Abstract: Highly Selective Amidation of Benzylic Alcohols with Nitriles. A Modified Ritter Reaction." ChemInform 25, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.199441099.

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9

Hassan, Ghasemnejad-Bosra, and Habibzadeh Setareh. "Amberlite IR-120 catalyzed, microwave-assisted one-pot synthesis of amides from nitriles by Ritter reaction." Journal of Indian Chemical Society Vol. 91, Jan 2014 (2014): 117–21. https://doi.org/10.5281/zenodo.5636369.

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Department of Chemistry, Islamic Azad University-Babol Branch, Babol, Iran E-mail : h_ghasem2000@yahoo.it Fax : 98-111-2415132 Industrial Noshiravani University, Babol, Iran Manuscript received online 13 January 2013, revised 09 February 2013, accepted 05 March 2013 <strong>A variety of alkenes and alcohols undergo one-pot amidation with nitriles in the presence of amberlite IR&shy;120 as a mild and effective catalyst under microwave irradiation and mild conditions to afford the corresponding secondary amides in good to excellent yields. This is a highly efficient method for the preparation of
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10

Hassan, Ghasemnejad-Bosra, and Habibzadeh Setareh. "Amberlite IR-120 catalyzed, microwave-assisted one-pot synthesis of amides from nitriles by Ritter reaction." Journal Of Indian Chemical Society Vol. 91, Jan 2014 (2014): 117–21. https://doi.org/10.5281/zenodo.5746682.

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Abstract:
Department of Chemistry, Islamic Azad University-Babol Branch, Babol, Iran <em>E-mail</em> : h_ghasem2000@yahoo.it Fax : 98-111-2415132 Industrial Noshiravani University, Babol, Iran <em>Manuscript received online 13 January 2013, revised 09 February 2013, accepted 05 March 2013</em> A variety of alkenes and alcohols undergo one-pot amidation with nitriles in the presence of amberlite <strong>IR-120</strong> as a mild and effective catalyst under microwave irradiation and mild conditions to afford the corresponding secondary amides in good to excellent yields. This is a highly efficient method
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