Mohinder P. Mahajan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Mohinder P. Mahajan has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Gaurav Bhargava
Department of Chemistry I. K. Gujral Punjab Technical University Kapurthala Punjab India
3 shared publications Takao Saito
2 shared publications- Vipan Kumar
Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, Punjab, India
2 shared publications Amit Anand
1 shared publication- Arun K. Sharma
Department of Molecular and Precision Medicine, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA
1 shared publication Gurleen Kaur
School of Pharmaceutical Sciences, Apeejay Stya University, Plot No. 23, Institutional Area, Sector-32, Gurgaon 122001, India
1 shared publication
Latest Publications
- 1 April 2016
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 26 (8) , 1963-1969
Design, synthesis, and anti-breast cancer evaluation of new triarylethylene analogs bearing short alkyl- and polar amino-/amido-ethyl chains
- 1 April 2016
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 26 (8) , 1963-1969
Design, synthesis, and anti-breast cancer evaluation of new triarylethylene analogs bearing short alkyl- and polar amino-/amido-ethyl chains
- 30 March 2011
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2011 (14) , 2697-2704
β‐Lactam‐Synthon‐Interceded, Facile, One‐Pot, Diastereoselective Synthesis of Functionalized Tetra/Octahydroisoquinolone Derivatives
The convenient and facile synthesis of tetra/octahydroisoquinolones has been developed and validated by using inter/intramolecular amidolysis of racemic N‐aryl‐β‐lactams followed by intramolecular iodocyclization protocols. Thesingle‐pot synthetic version of the desired conversion was successfully developed. The single‐pot synthesis of tetrahydro‐4H‐isoquinoline‐1,3‐diones invariably resulted in aromatic electrophilic iodination rather than the desired iodocyclization in cases where N‐phenyl‐2‐azetidinones were employed as the synthetic precursors.
- 30 March 2011
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2011 (14) , 2697-2704
β‐Lactam‐Synthon‐Interceded, Facile, One‐Pot, Diastereoselective Synthesis of Functionalized Tetra/Octahydroisoquinolone Derivatives
The convenient and facile synthesis of tetra/octahydroisoquinolones has been developed and validated by using inter/intramolecular amidolysis of racemic N‐aryl‐β‐lactams followed by intramolecular iodocyclization protocols. Thesingle‐pot synthetic version of the desired conversion was successfully developed. The single‐pot synthesis of tetrahydro‐4H‐isoquinoline‐1,3‐diones invariably resulted in aromatic electrophilic iodination rather than the desired iodocyclization in cases where N‐phenyl‐2‐azetidinones were employed as the synthetic precursors.
- 17 March 2008
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 2008 (07) , 983-986
Regio- and Chemoselective Unprecedented Imino-Diels-Alder Reactions of 1-Substituted Unactivated Dienes with N-Aryl Imines - Part II
The chemo- as well as regioselective participation of N-aryl imines as 4π component in aza-Diels-Alder reactions with 3-butadienyl-2-azetidinones in the presence of Lewis acid catalysts resulting in novel quinoline derivatives is described.
- 17 March 2008
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 2008 (07) , 983-986
Regio- and Chemoselective Unprecedented Imino-Diels-Alder Reactions of 1-Substituted Unactivated Dienes with N-Aryl Imines - Part II
The chemo- as well as regioselective participation of N-aryl imines as 4π component in aza-Diels-Alder reactions with 3-butadienyl-2-azetidinones in the presence of Lewis acid catalysts resulting in novel quinoline derivatives is described.
- 24 August 2006
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 2006 (14) , 2199-2202
SeO2-Mediated Oxidation of 1,3-Diazabuta-1,3-dienes: A Single-Pot Synthesis of Functionalized 4-Hydroxyimidazoles
A single-pot novel synthesis of variedly substituted 4-hydroxyimidazoles by SeO2-mediated oxidation of 1-aryl-2-phenyl/thiomethyl/secondary amino-4-N,N-dimethylamino-4-methyl-1,3-diazabuta-1,3-dienes is reported.
- 24 August 2006
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 2006 (14) , 2199-2202
SeO2-Mediated Oxidation of 1,3-Diazabuta-1,3-dienes: A Single-Pot Synthesis of Functionalized 4-Hydroxyimidazoles
A single-pot novel synthesis of variedly substituted 4-hydroxyimidazoles by SeO2-mediated oxidation of 1-aryl-2-phenyl/thiomethyl/secondary amino-4-N,N-dimethylamino-4-methyl-1,3-diazabuta-1,3-dienes is reported.
- 25 May 2005
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2005 (11) , 2397-2405
Highly Diasteroselective and Remarkably π‐Facially Selective Lewis Acid‐Catalysed Diels–Alder Cycloaddition Reactions: Access to Novel 1,3,4‐Trisubstituted 2‐Azetidinones
Diastereoselective and π‐facially selective Lewis acid‐catalysed intermolecular Diels–Alder reactions of 3‐butadienylazetidin‐2‐ones with a variety of symmetrical dienophiles (maleic anhydride, N‐phenylmaleimide, N‐p‐tolylmaleimide, benzoquinone and naphthoquinone) resulting in the synthesis of diastereomerically pure 1,3,4‐trisubstituted 2‐azetidinones are reported. The effects of different Lewis acids on the yields of the selectively formed diastereoisomers under different reaction conditions are also examined. Preferential chelation between the Lewis acid complexes of the different dienophiles and the carbonyl oxygens in the dienylazetidin‐2‐ones has been invoked to explain the observed π‐facial selectivity. The Lewis acid complexes of the dienophiles have been shown to approach preferentially from the si‐faces of the dienes, resulting in the formation of π‐facially selective “endo” adducts. The structures of these “endo” adducts have even been supported by X‐ray diffraction studies. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)
- 25 May 2005
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2005 (11) , 2397-2405
Highly Diasteroselective and Remarkably π‐Facially Selective Lewis Acid‐Catalysed Diels–Alder Cycloaddition Reactions: Access to Novel 1,3,4‐Trisubstituted 2‐Azetidinones
Diastereoselective and π‐facially selective Lewis acid‐catalysed intermolecular Diels–Alder reactions of 3‐butadienylazetidin‐2‐ones with a variety of symmetrical dienophiles (maleic anhydride, N‐phenylmaleimide, N‐p‐tolylmaleimide, benzoquinone and naphthoquinone) resulting in the synthesis of diastereomerically pure 1,3,4‐trisubstituted 2‐azetidinones are reported. The effects of different Lewis acids on the yields of the selectively formed diastereoisomers under different reaction conditions are also examined. Preferential chelation between the Lewis acid complexes of the different dienophiles and the carbonyl oxygens in the dienylazetidin‐2‐ones has been invoked to explain the observed π‐facial selectivity. The Lewis acid complexes of the dienophiles have been shown to approach preferentially from the si‐faces of the dienes, resulting in the formation of π‐facially selective “endo” adducts. The structures of these “endo” adducts have even been supported by X‐ray diffraction studies. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)