Mahmoud Nassiri

ORCID: 0000-0002-3388-9470
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Phosphorus compounds and reactions
  • Multicomponent Synthesis of Heterocycles
  • Synthesis and biological activity
  • Synthesis and Reactivity of Sulfur-Containing Compounds
  • Synthetic Organic Chemistry Methods
  • Synthesis and Biological Evaluation
  • Organophosphorus compounds synthesis
  • Click Chemistry and Applications
  • Chemical Synthesis and Analysis
  • Cytomegalovirus and herpesvirus research
  • Synthesis and Reactivity of Heterocycles
  • Synthesis and Characterization of Heterocyclic Compounds
  • Synthesis of Organic Compounds
  • Quinazolinone synthesis and applications
  • Oxidative Organic Chemistry Reactions
  • Synthesis and Characterization of Pyrroles
  • Analytical chemistry methods development
  • Synthesis of heterocyclic compounds
  • HIV/AIDS drug development and treatment
  • Biochemical and Molecular Research
  • Synthesis and Reactions of Organic Compounds
  • Carbohydrate Chemistry and Synthesis
  • Water Quality Monitoring and Analysis
  • HIV Research and Treatment
  • Synthesis and Biological Activity

Chabahar Maritime University
2014-2024

International University of Chabahar
2013

University of Sistan and Baluchestan
2005-2011

Lake Erie College of Osteopathic Medicine
1998-2003

Biolog (United States)
1991-2002

University of Michigan
1989-1999

Michigan Medicine
1991

PharmChem (United States)
1991

Ann Arbor Center for Independent Living
1989

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDesign, Synthesis, and Antiviral Activity of Certain 2,5,6-Trihalo-1-(.beta.-D-ribofuranosyl)benzimidazolesLeroy B. Townsend, Rodrigo V. Devivar, Steven R. Turk, M. Reza Nassiri, John C. DrachCite this: J. Med. Chem. 1995, 38, 20, 4098–4105Publication Date (Print):September 1, 1995Publication History Published online1 May 2002Published inissue 1 September...

10.1021/jm00020a025 article EN Journal of Medicinal Chemistry 1995-09-01

The combined cytotoxicity of zidovudine and ganciclovir in three cell lines human origin was examined. data were generated by a new rapid proliferation assay more sensitive plating efficiency assay. A three-dimensional analytical approach used to evaluate the drug-drug interactions, results compared with those obtained two conventional methods analysis. Synergistic observed all examined both assays. Moreover, this synergistic statistically significant at physiologically relevant...

10.1128/aac.35.6.1060 article EN Antimicrobial Agents and Chemotherapy 1991-06-01

Stable crystalline phosphorus ylides were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and dialkyl acetylenedicarboxylates presence of strong NH-acids, such as benzotriazole, 5-methylbenzotriazole, 5-chlorobenzotriazole, pyrrole, 2-acetylpyrrole, pyrrole-2-carboxaldehyde, 4-nitro-acetanilide, 4-methoxyacetanilide, 4-bromoacetanilide, 4-methylacetanilide, 2-methyl-acetanilide, 2,6-dimethylacetanilide. These stable exist a solution mixture two...

10.1080/10426500500272111 article EN Phosphorus, sulfur, and silicon and the related elements 2006-03-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSynthesis, cytotoxicity, and antiviral activity of some acyclic analogs the pyrrolo[2,3-d]pyrimidine nucleoside antibiotics tubercidin, toyocamycin, sangivamycinPranab K. Gupta, Sylvia Daunert, M. Reza Nassiri, Linda L. Wotring, John C. Drach, Leroy B. TownsendCite this: J. Med. Chem. 1989, 32, 2, 402–408Publication Date (Print):February 1, 1989Publication History Published online1 May 2002Published inissue 1 February...

10.1021/jm00122a019 article EN Journal of Medicinal Chemistry 1989-02-01

The sodium salts of 4-chloro- and several 4-chloro-5-substituted-7H-pyrrolo[2,3-d]pyrimidines were treated with [1,3-bis(benzyloxy)-2-propoxy]methyl chloride (6) to provide the corresponding 4-chloro-5-substituted-7-[[1,3-bis(benzyloxy)-2-propoxy]methyl]pyrrolo [2,3-d]pyrimidines (7-11). Debenzylation boron trichloride at -78 degrees C furnished 4-chloro-5-substituted-7-[(1,3-dihydroxy-2-propoxy)methyl]pyrrolo[2,3- d]pyrimidines (12.16). Subsequent amination 12-16 yielded...

10.1021/jm00169a028 article EN Journal of Medicinal Chemistry 1990-07-01

In this work, a new series of 1,2-diphenyl-3aH-spiro[benzo[d]pyrrolo[2,1-b]thaizol-3,5ʹ-pyrimidine (4) or 3,2ʹ-indendion (6) derivatives were efficiently designed and prepared using novel easy route in excellent yields by multicomponent-reactions between benzothiazoles, 2-chloro-2-phenylacetophenone, 1,3-dicarbonyl compounds. These reactions carried out CH2Cl2 at ambient temperature under catalyst-free conditions for 3 h. The structure all the synthesized compounds established NMR, IR, EI-MS...

10.1016/j.rechem.2024.101676 article EN cc-by Results in Chemistry 2024-07-01

Stable crystalline phosphorus ylides were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and dialkyl acetylenedicarboxylates, presence of strong NH-acids, such as imidazole, 2-methylimidazole, 4-methylimidazole, 2-ethylimidazole, benzimidazole, 5,6-dimethylbezimidazole. These stable exist solution a mixture two geometrical isomers result restricted rotation around carbon–carbon partial double bond resulting conjugation ylide moiety with adjacent...

10.1080/10426500500267624 article EN Phosphorus, sulfur, and silicon and the related elements 2006-03-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSynthesis, cytotoxicity, and antiviral activity of certain 7-[(2-hydroxyethoxy)methyl]pyrrolo[2,3-d]pyrimidine nucleosides related to toyocamycin sangivamycinPranab K. Gupta, M. Reza Nassiri, Lisa A. Coleman, Linda L. Wotring, John C. Drach, Leroy B. TownsendCite this: J. Med. Chem. 1989, 32, 7, 1420–1425Publication Date (Print):July 1, 1989Publication History Published online1 May 2002Published inissue 1 July...

10.1021/jm00127a003 article EN Journal of Medicinal Chemistry 1989-07-01

In this study, arylglyoxals, acetylacetone, and 2,6-dimethyl phenol or 2,6-di-tert-butyl are combined to efficiently synthesize a series of 1-(4-(3,5-dialkylphenyl)-2-methyl-5-phenylfuran-3-yl) ethan-1-one derivatives in excellent yields. These reactions were carried out acetone at reflux under catalyst-free conditions the presence triethylamine as base for 3 h. NMR, FT-IR, EI-MS, elemental studies used characterize products' structural characteristics. The present study has also several...

10.55730/1300-0527.3649 article EN TURKISH JOURNAL OF CHEMISTRY 2024-02-21

Stable crystalline phosphorus ylides were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and dialkyl acetylenedicarboxylates, presence of strong NH-acids, such as pyrazole, indazole 5-nitro Indazole. These stable exist solution a mixture two geometrical isomers result restricted rotation around carbon–carbon partial double bond resulting conjugation ylide moiety with adjacent carbonyl group.

10.1080/104265090968479 article EN Phosphorus, sulfur, and silicon and the related elements 2005-12-13

Abstract Stable crystalline phosphorus ylides were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and dialkyl acetylenedicarboxylates, presence of NH‐acid, such as 3,6‐dibromocarbazole. These stable exist solution a mixture two geometrical isomers result restricted rotation around carbon–carbon partial double bond, resulting conjugation ylide moiety with adjacent carbonyl group. To determine kinetic parameters reactions, they monitored by UV...

10.1002/hc.20501 article EN Heteroatom Chemistry 2008-11-01

Stable crystalline phosphorus ylides containing chlorine and sulfur were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine dialkyl acetylene-dicarboxylates presence of 6-chloro-2-benzoxazolethiol 2-chloro-phenothiazine. These stable exist solution as a mixture two geometrical isomers. This is caused by conjugation ylide moiety with adjacent carbonyl group, which results restricted rotation around respective carbon-carbon bond.

10.1080/10426500802275093 article EN Phosphorus, sulfur, and silicon and the related elements 2009-06-26

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSynthesis and Antiproliferative Antiviral Activity of 2'-Deoxy-2'-fluoroarabinofuranosyl Analogs the Nucleoside Antibiotics Toyocamycin SangivamycinSteven H. Krawczyk, M. Reza Nassiri, Louis S. Kucera, Earl R. Kern, Roger G. Ptak, Linda L. Wotring, John C. Drach, Leory B. TownsendCite this: J. Med. Chem. 1995, 38, 20, 4106–4114Publication Date (Print):September 1, 1995Publication History Published online1 May 2002Published inissue 1 September...

10.1021/jm00020a026 article EN Journal of Medicinal Chemistry 1995-09-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTSynthesis and antiviral activity of certain 4- 4,5-disubstituted 7-[(2-hydroxyethoxy)methyl]pyrrolo[2,3-d]pyrimidinesJeffrey S. Pudlo, Naveen K. Saxena, M. Reza Nassiri, Steven R. Turk, John C. Drach, Leroy B. TownsendCite this: J. Med. Chem. 1988, 31, 11, 2086–2092Publication Date (Print):November 1, 1988Publication History Published online1 May 2002Published inissue 1 November...

10.1021/jm00119a006 article EN Journal of Medicinal Chemistry 1988-11-01

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199604258 article EN ChemInform 1996-01-23

Stable crystalline phosphorus ylides were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and dialkyl acetylenedicarboxylates presence of strong SH-acids, such as 2-mercapto-1-methylimidazole 2-thiazoline-2-thiol. These stable exist solution a mixture two geometrical isomers result restricted rotation around carbon–carbon partial double bond resulting conjugation ylide moiety with adjacent carbonyl group.

10.1080/17415990500276238 article EN Journal of Sulfur Chemistry 2005-06-01

The reaction between dialkyl acetylenedicarboxylates and N-H acids such as pyrazole indazole in the presence of triphenylphosphite at room temperature led to stable phosphonate ester derivatives 4a-f.The configuration compounds 4a-f (2S * ,3R ) was determined on basis coupling constants predicted from Karplus equation.

10.3998/ark.5550190.0007.c17 article EN cc-by ARKIVOC 2006-08-24

Stable crystalline phosphorus ylides were obtained in excellent yields from the 1:1:1 addition reaction between triphenylphosphine and dialkyl acetylenedicarboxylates presence of strong NH acids, such as indole 2-methyl indole, 3-methyl 5-boromo indole. These stable exist a solution mixture two geometrical isomers result restricted rotation around carbon–carbon partial double bond resulting conjugation ylide moiety with adjacent carbonyl group.

10.1080/10426500500272160 article EN Phosphorus, sulfur, and silicon and the related elements 2006-03-01
Coming Soon ...