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Dive into the research topics where Galal H. Elgemeie is active.

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Featured researches published by Galal H. Elgemeie.


Tetrahedron | 1997

SYNTHESIS OF SOME NOVEL CONDENSED PYRIDINE-2(1H)-THIONES AND RELATED GLYCOSIDES

Adel M. Attia; Galal H. Elgemeie; Lamies A. Shahada

Abstract A novel synthesis of condensed pyridine-2(1 H )-thiones and 3-deazapyrimidine glycosides is described utilizing arylmethylenecyanothioacetamides and dimedone as starting components.


Nucleosides, Nucleotides & Nucleic Acids | 1999

SYNTHESIS AND ANTI-HIV ACTIVITY OF DIFFERENT NOVEL NONCLASSICAL NUCLEOSIDES

Galal H. Elgemeie; Omar A. Mansour; Nadia H. Metwally

A series of different novel nonclassical nucleosides have been synthesised and evaluated for their inhibitory activity against human immunodeficiency virus (HIV) replication in MT-4 cells.


Journal of Carbohydrate Chemistry | 2009

First Synthesis of Thiophene Thioglycosides

Galal H. Elgemeie; Wafaa A. Zaghary; Kamelia M. Amin; Tamer Nasr

A new method for the preparation of a new class of thiophene thioglycosides via one-pot reaction of the sodium thiophenethiolate salts with 2,3,4,6-tetra-O-acetyl-α-D-gluco- and galacto-pyranosyl bromides has been studied. The sodium thiophenethiolate salts are prepared using cyano-di-thioic analogs and their corresponding mono- and dithiolate salts.


Nucleosides, Nucleotides & Nucleic Acids | 2005

New Trends in Synthesis of Pyrazole Nucleosides as New Antimetabolites

Galal H. Elgemeie; Wafaa A. Zaghary; Kamelia M. Amin; Tamer Nasr

Pyrazole nucleosides and condensed pyrazole nucleosides exhibit various biological activities. This article describes recent synthetic approaches to their preparation, chemical properties, biological activities, and structure-activity relationships, with emphasis to selected drugs or drug candidates. Two pyrazole C-nucleoside compounds pyrazofurin (pyrazomycin) and its α-epimer pyrazofurin B are active components of potent antivirals approved for therapeutic use in human medicine aimed against various diseases caused by DNA viruses.


Synthetic Communications | 2002

Potential purine analogue antagonists: Synthesis of novel cycloalkane ring-fused pyrazolo[1,5-a]pyrimidines

Galal H. Elgemeie; Hany A. Ali

ABSTRACT A convenient route for the synthesis of new variety of pyrazolo[1,5-a]pyrimidine derivatives by the reaction of 5-aminopyrazoles with suitable unsaturated keto compounds. The structure of the reaction products were established based on the elemental analysis, spectral data (IR, 1H NMR, MS) and X-ray diffraction analysis.


Synthetic Communications | 2001

REACTIONS OF CHLOROCARBONYL ISOCYANATE WITH 5-AMINOPYRAZOLES AND ACTIVE METHYLENE NITRILES: A NOVEL SYNTHESIS OF PYRAZOLO[1,5-a]-1,3,5-TRIAZINES AND BARBITURATES

Galal H. Elgemeie; Samia R. El-Ezbawy; Hany A. Ali

Reactions of chlorocarbonyl isocyanate and chlorosulfonyl isocyanate with aminopyrazoles and active methylene nitriles are reported. They lead to novel pyrazolo[1,5-a]-1,3,5-triazines and barbituric acid derivatives. The structures of the products and the mechanisms of their formation are reported.


Synthetic Communications | 2001

THE DESIGN AND SYNTHESIS OF STRUCTURALLY RELATED MERCAPTOPURINE ANALOGUES: REACTION OF DIMETHYL N-CYANO-DITHIOIMINOCARBONATE WITH 5-AMINOPYRAZOLES

Galal H. Elgemeie; Samia R. El-Ezbawy; Hany A. El-Aziz

A novel synthesis of 4-methylthiopyrazolo[1,5-a]-1,3,5-triazines via reaction of dimethyl N-cyanodithioiminocarbonate with 5-aminopyrazoles is reported and the synthetic potential of the method is demonstrated.


Journal of Carbohydrate Chemistry | 2008

First Synthesis of Thienopyrazole Thioglycosides

Galal H. Elgemeie; Wafaa A. Zaghary; Tamer Nasr; Kamelia M. Amin

Reported is the first method to prepare a new class of thienopyrazole thioglycosides via a one‐pot reaction of the sodium thienopyrazolthiolate salts with 2,3,4,6‐tetra‐O‐acetyl‐α‐D‐gluco‐and galactopyranosyl bromides. The sodium thienopyrazolthiolate salts are prepared using pyrazoldithioic acids and their corresponding mono ‐ and dithiolate salts.


Synthetic Communications | 2003

A New Class of Dihydropyridine Thioglycosides via Piperidinium Salts

Adel M. E. Attia; Galal H. Elgemeie

Abstract A first reported method for preparation of a new class of thioglycosides via reaction of piperidinium salts of dihydropyridinethiones with 2,3,4,6-tetra-O-acetyl-α-d-gluco- and galactopyranosyl bromides has been studied. Comparison with the products obtained from silylated thiopyridines is made.


Nucleosides, Nucleotides & Nucleic Acids | 2000

Nucleic acid components and their analogues: new synthesis of bicyclic thiopyrimidine nucleosides.

Galal H. Elgemeie; Adel M. E. Attia; Sherifa S. Alkabai

Abstract A novel synthesis of condensed bicyclic thiopyrimidine glycosides utilising 1H-cyclopentapyrimidine-2(3H)-thiones and α-bromoglucose or α-bromogalactose tetraacetate as starting components is described.

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Peter G. Jones

Braunschweig University of Technology

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