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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 33, 2003 - Issue 7
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Original Articles

Introduction of a Carbohydrate Moiety into the Structure of Thiourea Compounds Targeting HIV-1 Reverse Transcriptase

P. Mallikarjun Goud Department of Chemistry, Parker Hughes Institute, Roseville, Minnesota, USA
,
T. K. Venkatachalam Department of Chemistry, Parker Hughes Institute, Roseville, Minnesota, USA
&
F. M. Uckun M.D., Ph.D. Department of Chemistry, Parker Hughes Institute, Roseville, Minnesota, USACorrespondence[email protected]
Pages 1185-1193 | Received 15 May 2002, Published online: 21 Aug 2006

Citations (8)

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Read on this site (4)

Kunj B. Mishra, Sanchayita Rajkhowa & Vinod K. Tiwari. (2020) An expeditious one-pot synthesis of thiourea derivatives of carbohydrates from sugar azides. Journal of Carbohydrate Chemistry 39:7, pages 334-353.
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T. K. Venkatachalam & F. M. Uckun. (2007) Synthesis of Substituted Heterocyclic Thiourea Compounds. Synthetic Communications 37:20, pages 3667-3675.
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T. K. Venkatachalam & F. M. Uckun. (2006) Synthesis of Heterocyclic Thiourea Compounds with Amino Acid Side Chain as Nonnucleoside Inhibitors of HIV‐1 Reverse Transcriptase. Synthetic Communications 36:15, pages 2103-2112.
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T. K. Venkatachalam & F. M. Uckun. (2005) Synthesis of Symmetrical and Asymmetrical Phenethyl Thiourea Compounds as Nonnucleoside Inhibitors of HIV‐1 Reverse Transcriptase. Synthetic Communications 35:15, pages 2039-2056.
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Articles from other publishers (4)

Fahad Hussain, Fahad Imtiaz Rahman, Poushali Saha, Atsushi Mikami, Takashi Osawa, Satoshi Obika & S. M. Abdur Rahman. (2022) Synthesis of Sugar and Nucleoside Analogs and Evaluation of Their Anticancer and Analgesic Potentials. Molecules 27:11, pages 3499.
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Pavel А. Volkov, Nina I. Ivanova, Nina K. Gusarova, Boris G. Sukhov, Kseniya O. Khrapova, Lev E. Zelenkov, Vladimir I. Smirnov, Tatyana N. Borodina, Tamara I. Vakul'skaya, Spartak S. Khutsishvili & Boris A. Trofimov. (2015) Expedient Route to Chalcogenophosphinates with Glucose Moieties via Todd-Atherton-Like Coupling between Secondary Phosphine Chalcogenides and Diacetone- d -Glucose in the CCl 4 /Et 3 N System . Heteroatom Chemistry 26:5, pages 329-334.
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Justyna A. Grzyb, Ming Shen, Chiaki Yoshina-Ishii, W. Chi, R.Stanley Brown & Robert A. Batey. (2005) Carbamoylimidazolium and thiocarbamoylimidazolium salts: novel reagents for the synthesis of ureas, thioureas, carbamates, thiocarbamates and amides. Tetrahedron 61:30, pages 7153-7175.
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P. Mallikarjun Goud, T. K. Venkatachalam & F. M. Uckun. (2003) Introduction of a Carbohydrate Moiety into the Structure of Thiourea Compounds Targeting HIV‐1 Reverse Transcriptase.. ChemInform 34:35.
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