Dr Virender Singh
Dr Virender Singh
Verified email at nitj.ac.in - Homepage
Title
Cited by
Cited by
Year
Medicinal attributes of 1,2,3-triazoles: Current developments
RS D. Dheer, Virender Singh
Bioorganic Chemistry 71, 30-54, 2017
4652017
Diversity Oriented Synthesis of Fused-imidazole Derivatives via Groebke-Blackburn-Bienayme Reaction: A Review
RKRVS N. Devi
Tetrahedron 71, 183-232, 2015
1032015
Synthetic and medicinal perspective of thiazolidinones: A review.
RKR S. K. Manjal, R. Kaur, R. Bhatia, K. Kumar, Virender Singh, R. Shankar ...
Bioorganic Chemistry 75, 406-423, 2017
872017
An alternate approach to quinoline architectire via Baylis-Hillman chemistry: SnCl2-mediated tandem reaction toward synthesis of 4-(substituted vinyl)-quinolines
VSSB S. Madapa
Tetrahedron 62, 2006
512006
Medicinal Attributes of Imidazo[1,2-a]pyridine Derivatives: An Update
VS N. Devi, D. Singh, R. K. Rawal, J. Bariwal
Curr. Top. Med. Chem 16, DOI: 10.2174/1568026616666160506145539, 2016
41*2016
Synthesis of substituted 3-methylene-2-pyridones from Baylis-Hillman derivatives and its application for the generation of 2-pyridone substituted spiroisoxazolines
PRMSB Virender Singh, G. P. Yadav
Tetrahedron 64, 2979-2991, 2008
402008
In(OTf)3 Assisted Synthesis of β-Carboline C-3 Tethered Imidazo[1,2-a]azine Derivatives.
CCMVS N. Devi, D. Singh, G. Kaur, S. Mor
New Journal of Chemistry 41, 1082-1093, 2017
312017
Metal-free Decarboxylative Amination: An Alternative Approach towards Regioselective Synthesis of β-Carboline N-fused Imidazoles
RSVS D. Singh, V. Kumar, N. Devi, C. C. Malakar
Adv. Synth. Catal. 359, 1213-1226., 2017
292017
Natural Product Inspired Designing and Synthesis of β-Carboline and γ-Lactones Based Molecular Hybrids
VS D. Singh, N. Devi, V. Kumar, C. C. Malakar, S. Mehra, S. Rattan, R. K. Rawal
Organic & Biomolecular Chemistry 14, 8154-8166, 2016
292016
1 (3)‐Formyl‐β‐carbolines: Potential Aldo‐X Precursors for the Synthesis of β‐Carboline‐Based Molecular Architectures
N Devi, S Kumar, SK Pandey, V Singh
Asian Journal of Organic Chemistry 7 (1), 6-36, 2018
282018
ZnO Nanoparticles as reusable heterogeneous catalyst for efficient one pot three component synthesis of imidazo-fused polyheterocycles
RS S. Swami, N. Devi, A. Agarwala, Virender Singh
Tetrahedron Letters 57, 1346-1350, 2016
272016
1-Formyl-9H-β-carboline: A useful scaffold for synthesizing substituted- and fused β-carbolines
VSS Batra
Curr. Org. Syn. 2012, 9, 513-528 9, 513-528, 2012
27*2012
β-CD/CuI catalyzed regioselective synthesis of iodo substituted 1,2,3-triazoles, imidazo[1, 2-a]-pyridines and benzoimidazo[2,1-b]thiazoles in water and their functionalization.
RS D. Dheer, R. K. Rawal, Virender Singh, P. Sangwan, P. Das
Tetrahedron 73, 4295–4306, 2017
252017
Baylis-Hillman reaction of 1-formyl-β-carboline: One-step synthesis of the canthin-6-one framework by an unprecedented cascade cyclization reaction
V Singh, S Hutait, S Batra
Eur. J. Org. Chem 2009, 6211-6216, 2009
252009
Versatility of substituted 1-formyl-9H-β-carbolines for the syntheses of new fused β-carbolines via intramolecular 1,3-Dipolar Cycloaddition
SBSB Virender Singh, S. Hutait
Eur. J. Org. Chem., 531-539, 2010
212010
Straight forward strategy for stereoselective synthesis of spiro-fused (C-5)isoxazolino or (C-3)pyrazolino-(C-3)-quinolin-2-ones from Baylis-Hillman adducts via 1,3-dipolar …
VSSB Virender Singh
Eur. J. Org. Chem., 5446-5460, 2008
212008
Synthetic and Medicinal Prospective of Structurally Modified Curcumins
KKRKR B. Kumar, Virender Singh, R. Shankar
Curr. Top. Med. Chem, 2016
20*2016
In(OTf)3 Catalysed an Expeditious Synthesis of β-Carboline- imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrazine Conjugates
VS N. Devi, D. Singh, Honey, S. Mor, S. Chaudhary, R. K Rawal, V. Kumar, A ...
RSC Advances 6, 43881-43891, 2016
202016
Studies on the Baylis-Hillman reaction of pyrazolecarbaldehydes under the influence of DABCO: Positional effect on the reactivity of the formyl group
VSSB S. Nag
ARKIVOC 14, 185-203, 2007
192007
Reductive-cyclization-mediated syntheses of fused polycyclic quinolines from the Baylis-Hillman adducts of acrylonitrile: Scope and limitati
SHSB Virender Singh
Eur. J. Org. Chem., 3454-3466, 2009
17*2009
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