Search Results - "Madhubabu, M V"

Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compounds by Murthy, V Narayana, Nikumbh, Satish P, Tadiparthi, Krishnaji, Madhubabu, M V, Jammula, Subba Rao, Rao, L Vaikunta, Raghunadh, Akula

“…A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a…”
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Efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones catalyzed by titanium silicon oxide nanopowder in aqueous media by Mekala, Ramamohan, Madhubabu, M. V., Dhanunjaya, G., Regati, Sridhar, Chandrasekhar, K. B., Sarva, Jayaprakash

“…An efficient synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives is accomplished in aqueous media by a three-component reaction of isatoic anhydride,…”
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Green and Efficient One-Pot Synthesis of 9-(1H-Indol-2-yl)-5,6,7,9-tetrahydrotetrazolo[5,1-b]quinazolin-8(4H)-ones by Prakash, P. S., Madhubabu, M. V., Arunkumar, T., Jaganmohan, C., Rao, B. Venkateswara, Raghunadh, A.

“…The indole-conjugated tetrazolo and quinazoline scaffolds play a pivotal role in the composition of various novel chemical compounds renowned for their…”
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An Orthogonal Approach for Determination of Acetamide Content in Pharmaceutical Drug Substance and Base-Contaminated Acetonitrile by GC and GC-MS External Method by Rajana, Nagaraju, Yarbagi, Kaviaraj M, Balakumaran, K, Madhubabu, M V, Mosesbabu, J, Basavaiah, K, Rama Devi, Dharamasoth

“…Acetamide is a potential genotoxic impurity; it should control in drug substance based on daily dosage level. It forms from base-contaminated acetonitrile and…”
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Synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives as potential inhibitors of TNF-α by Dhananjaya, G., Venkateshwarlu, Rapolu, Madhubabu, M.V., Raghunadh, Akula, Murthy, V. Narayana, Reddy, S. Pulla, Anna, Venkateswara Rao, Kapavarapu, Ravikumar, Pal, Manojit

“…•2,3-Dihydroquinazolin-4(1H)-ones were explored as potential TNF-α inhibitors.•β-CD catalyzed reaction in pure water was used to synthesize these compounds.•At…”
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Metal–Catalyst-Free Green and efficient synthesis of five and six membered fused N-heterocyclic quinazoline derivatives by Madhubabu, M.V., Shankar, R., Reddy, G. Rajeshwar, Rao, T. Srinivasa, Basaveswara Rao, Mandava V., Akula, Raghunadh

“…[Display omitted] •An efficient and green approach for the synthesis of Tetracyclic nitrogen-bridgehead compounds.•Synthetic approach involves construction of…”
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A convergent approach towards the synthesis of the 2-alkyl-substituted tetrahydroquinoline alkaloid (−)-cuspareine by Madhubabu, M.V., Shankar, R., Krishna, T., Kumar, Y. Satish, Chiranjeevi, Y., Muralikrishna, Ch, Mohan, H. Rama, More, Satish S., Rao, M.V. Basaveswara, Akula, Raghunadh

“…[Display omitted] A convergent approach towards the synthesis of the 2-alkyl-substituted tetrahydroquinoline alkaloid (−)-cuspareine via enantiospecific…”
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Amberlite-15 promoted an unprecedented aza Michael rearrangement for one pot synthesis of dihydroquinazolinone compoundsElectronic supplementary information (ESI) available. See DOI: 10.1039/c8ra03308k by Murthy, V. Narayana, Nikumbh, Satish P, Tadiparthi, Krishnaji, Madhubabu, M. V, Jammula, Subba Rao, Rao, L. Vaikunta, Raghunadh, Akula

“…A new one pot multicomponent annulation strategy for the synthesis of various dihydroquinazolinone compounds has been developed using Amberlite-15 as a…”
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Synthesis of [beta]-Arylacyl/[beta]-Heteroarylacyl-[beta]-alkylidene Malonates and Their Application in Substituted Pyridone Synthesis by Wagh, Manoj Balu, Shankar, R, Mini, K, Krishnamohan, T, Madhubabu, M. V, Pal, Abir K, Jayaprakash, Sarva, Krishna, T, Dahanukar, Vilas, Kumar, U. K. Syam, Gill, C. H

“…A novel approach has been developed for the synthesis of [beta]-arylacyl/[beta]-heteroarylacyl-[beta]-alkylidine malonates in moderate to good yields by the…”
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Synthesis of β-Arylacyl/β-Heteroarylacyl-β-alkylidene Malonates and Their Application in Substituted Pyridone Synthesis by Wagh, Manoj Balu, Shankar, R., Mini, K., Krishnamohan, T., Madhubabu, M. V., Pal, Abir K., Jayaprakash, Sarva, Krishna, T., Dahanukar, Vilas, Kumar, U. K. Syam, Gill, C. H.

“…A novel approach has been developed for the synthesis of β‐arylacyl/β‐heteroarylacyl‐β‐alkylidine malonates in moderate to good yields by the reaction of Stork…”
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