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Papers by Kamal Dawood
Advanced Synthesis & Catalysis
Journal of Heterocyclic Chemistry
Expert Opinion on Therapeutic Patents
Molecules
Reactions of a series of 3-oxo-2-arylhydrazonopropanal derivatives with two molar ratio of ammoni... more Reactions of a series of 3-oxo-2-arylhydrazonopropanal derivatives with two molar ratio of ammonium acetate afforded a library of tetrasubstituted 2,3,6,7,9-pentaazabicyclo[3.3.1]nona- 3,7-diene derivatives in good to excellent isolated yields. The reaction was activated with triethylamine catalyst under three different heating modes: thermal, ultrasonic and microwave irradiating conditions in ethanol solvent. The structures of the isolated products were fully characterized by spectral and analytical data as well as X-ray single crystal of selected examples.
Journal of Heterocyclic Chemistry
Expert opinion on therapeutic patents, 2018
Several natural products containing benzosuberone moiety are clinically reported as anti-tumor ag... more Several natural products containing benzosuberone moiety are clinically reported as anti-tumor agents. Furthermore, several synthetic benzosuberones cited in this review exhibited wide range of theraputic activities such as bacteriostatic, anti-inflammatory, antidepressants and anti-tumor activities. Our recent review provides an overview of the different methods to synthesize the benzosuberones and their extensive biological activities. Areas covered: Thirty-two patents among 130 references are cited in this review that covered the recent inhibitory activities of the benzosuberone scaffolds and their broad area of biological applications up to the first quarter of 2017. The areas covered included anti-inflammatory, antimicrobial, antitumor, selective estrogen receptor, anti-obesity, beta-amyloid production, enzymes and HCV inhibitors in addition to anti-Alzheimer and anti-tuberculosis activities as well as several receptors antagonists. Expert opinion: It is important for medical a...
ChemInform
ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Expert Opinion on Therapeutic Patents, 2017
Four isomeric structures of thiadiazole motifs have outstanding pharmacological inhibitory applic... more Four isomeric structures of thiadiazole motifs have outstanding pharmacological inhibitory applications are reported in this review. Thiadiazole nucleus is present in several biologically active natural products and commercial drugs. Most of thiadiazoles reported herein are emphasized to have broad spectrum of medicinal activities. Areas covered: This review represents the recent inhibitory activities of thiadiazole isomeric scaffolds and their broad-spectrum biological applications published as full texts during 2010-2016 as well as the patents published during 2005-2016. The inhibition areas covered included anti-inflammatory, antimicrobial, antitumor, antioxidant, antitubercular, antiviral, antileishmanial, anticonvulsant, herbicidal and algicidal activities in addition to enzymes, human platelet aggregation and neuroprotective inhibitors. Expert opinion: This survey revealed very interesting data about the applications of thiadiazoles, where some synthetic or natural thiadiazole derivatives were components of drugs available in the market. Many thiadiazole derivatives can be considered as lead compounds for drug synthesis. The most inhibitory active 1,3,4-thiadiazole compounds are those incorporating secondary alkyl(aryl)amido- and/or benzylthio(mercapto) groups at positions 2 and 5. Several thiadiazole derivatives demonstrated higher antibacterial, antitumor and antiviral activities than the standard drugs. Some thiadiazole derivatives exhibited high selective enzymes inhibitory activities based on the electronic properties of the substituents at positions 2 or 5.
Journal of Chemical Research, Dec 1, 2004
3-(2-Furyl)-3-oxo-propanenitrile (1) reacts with some phosphorus ylides to afford new pyridazine ... more 3-(2-Furyl)-3-oxo-propanenitrile (1) reacts with some phosphorus ylides to afford new pyridazine and 1,2,4-triazine derivatives. Reaction of 1 with some heterocyclic diazonium salts afforded fused heterocyclic systems with bridgehead nitrogen atoms.
Synlett, Jul 1, 2009
ABSTRACT
Cheminform, Jun 1, 1999
ABSTRACT
Journal of Sulfur Chemistry, Aug 1, 2013
ABSTRACT
Heteroatom Chemistry, 2005
Phosphorus Sulfur and Silicon and the Related Elements, Nov 1, 1997
ABSTRACT
Tetrahedron Letters, Mar 26, 2001
Advanced Synthesis & Catalysis
Journal of Heterocyclic Chemistry
Expert Opinion on Therapeutic Patents
Molecules
Reactions of a series of 3-oxo-2-arylhydrazonopropanal derivatives with two molar ratio of ammoni... more Reactions of a series of 3-oxo-2-arylhydrazonopropanal derivatives with two molar ratio of ammonium acetate afforded a library of tetrasubstituted 2,3,6,7,9-pentaazabicyclo[3.3.1]nona- 3,7-diene derivatives in good to excellent isolated yields. The reaction was activated with triethylamine catalyst under three different heating modes: thermal, ultrasonic and microwave irradiating conditions in ethanol solvent. The structures of the isolated products were fully characterized by spectral and analytical data as well as X-ray single crystal of selected examples.
Journal of Heterocyclic Chemistry
Expert opinion on therapeutic patents, 2018
Several natural products containing benzosuberone moiety are clinically reported as anti-tumor ag... more Several natural products containing benzosuberone moiety are clinically reported as anti-tumor agents. Furthermore, several synthetic benzosuberones cited in this review exhibited wide range of theraputic activities such as bacteriostatic, anti-inflammatory, antidepressants and anti-tumor activities. Our recent review provides an overview of the different methods to synthesize the benzosuberones and their extensive biological activities. Areas covered: Thirty-two patents among 130 references are cited in this review that covered the recent inhibitory activities of the benzosuberone scaffolds and their broad area of biological applications up to the first quarter of 2017. The areas covered included anti-inflammatory, antimicrobial, antitumor, selective estrogen receptor, anti-obesity, beta-amyloid production, enzymes and HCV inhibitors in addition to anti-Alzheimer and anti-tuberculosis activities as well as several receptors antagonists. Expert opinion: It is important for medical a...
ChemInform
ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance t... more ABSTRACT ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Expert Opinion on Therapeutic Patents, 2017
Four isomeric structures of thiadiazole motifs have outstanding pharmacological inhibitory applic... more Four isomeric structures of thiadiazole motifs have outstanding pharmacological inhibitory applications are reported in this review. Thiadiazole nucleus is present in several biologically active natural products and commercial drugs. Most of thiadiazoles reported herein are emphasized to have broad spectrum of medicinal activities. Areas covered: This review represents the recent inhibitory activities of thiadiazole isomeric scaffolds and their broad-spectrum biological applications published as full texts during 2010-2016 as well as the patents published during 2005-2016. The inhibition areas covered included anti-inflammatory, antimicrobial, antitumor, antioxidant, antitubercular, antiviral, antileishmanial, anticonvulsant, herbicidal and algicidal activities in addition to enzymes, human platelet aggregation and neuroprotective inhibitors. Expert opinion: This survey revealed very interesting data about the applications of thiadiazoles, where some synthetic or natural thiadiazole derivatives were components of drugs available in the market. Many thiadiazole derivatives can be considered as lead compounds for drug synthesis. The most inhibitory active 1,3,4-thiadiazole compounds are those incorporating secondary alkyl(aryl)amido- and/or benzylthio(mercapto) groups at positions 2 and 5. Several thiadiazole derivatives demonstrated higher antibacterial, antitumor and antiviral activities than the standard drugs. Some thiadiazole derivatives exhibited high selective enzymes inhibitory activities based on the electronic properties of the substituents at positions 2 or 5.
Journal of Chemical Research, Dec 1, 2004
3-(2-Furyl)-3-oxo-propanenitrile (1) reacts with some phosphorus ylides to afford new pyridazine ... more 3-(2-Furyl)-3-oxo-propanenitrile (1) reacts with some phosphorus ylides to afford new pyridazine and 1,2,4-triazine derivatives. Reaction of 1 with some heterocyclic diazonium salts afforded fused heterocyclic systems with bridgehead nitrogen atoms.
Synlett, Jul 1, 2009
ABSTRACT
Cheminform, Jun 1, 1999
ABSTRACT
Journal of Sulfur Chemistry, Aug 1, 2013
ABSTRACT
Heteroatom Chemistry, 2005
Phosphorus Sulfur and Silicon and the Related Elements, Nov 1, 1997
ABSTRACT
Tetrahedron Letters, Mar 26, 2001