Manjunath Lamani
Affiliations: | 2008-2013 | Indian Institute of Science Bangalore |
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Parents
Sign in to add mentor| Kandikere R. Prabhu | grad student | 2008-2013 | IISc Bangalore |
| Alexandros Makriyannis | post-doc | Northeastern University |
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Publications
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| Malamas MS, Lamani M, Farah SI, et al. (2021) Design and Synthesis of Highly Potent and Specific ABHD6 Inhibitors. Chemmedchem |
| Kokona D, Spyridakos D, Tzatzarakis M, et al. (2021) The endocannabinoid 2-arachidonoylglycerol and dual ABHD6/MAGL enzyme inhibitors display neuroprotective and anti-inflammatory actions in the in vivo retinal model of AMPA excitotoxicity. Neuropharmacology. 185: 108450 |
| Malamas MS, Farah SI, Lamani M, et al. (2019) Design and synthesis of cyanamides as potent and selective N-acylethanolamine acid amidase inhibitors. Bioorganic & Medicinal Chemistry. 115195 |
| Lamani M, Malamas MS, Farah SI, et al. (2019) Piperidine and piperazine inhibitors of fatty acid amide hydrolase targeting excitotoxic pathology. Bioorganic & Medicinal Chemistry. 115096 |
| Nicolaou KC, Rhoades D, Lamani M, et al. (2016) Total Synthesis of Thailanstatin A. Journal of the American Chemical Society |
| Nicolaou KC, Shi L, Lu M, et al. (2014) Total synthesis of myceliothermophins C, D, and E. Angewandte Chemie (International Ed. in English). 53: 10970-4 |
| Siddaraju Y, Lamani M, Prabhu KR. (2014) A transition metal-free Minisci reaction: acylation of isoquinolines, quinolines, and quinoxaline. The Journal of Organic Chemistry. 79: 3856-65 |
| Dhineshkumar J, Lamani M, Alagiri K, et al. (2013) A versatile C-H functionalization of tetrahydroisoquinolines catalyzed by iodine at aerobic conditions. Organic Letters. 15: 1092-5 |
| Lamani M, Prabhu KR. (2012) NIS-catalyzed reactions: amidation of acetophenones and oxidative amination of propiophenones. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14638-42 |
| Lamani M, Guralamata RS, Prabhu KR. (2012) Guanidine catalyzed aerobic reduction: a selective aerobic hydrogenation of olefins using aqueous hydrazine. Chemical Communications (Cambridge, England). 48: 6583-5 |