Year |
Citation |
Score |
2023 |
Sivanandan ST, Nair DK, Namboothiri INN. Recent advances in the synthetic applications of Morita-Baylis-Hillman and Rauhut-Currier adducts of nitroalkenes. Organic & Biomolecular Chemistry. PMID 37486601 DOI: 10.1039/d3ob00853c |
0.555 |
|
2016 |
da Cruz EH, Silvers MA, Jardim GA, Resende JM, Cavalcanti BC, Bomfim IS, Pessoa C, de Simone CA, Botteselle GV, Braga AL, Nair DK, Namboothiri IN, Boothman DA, da Silva Júnior EN. Synthesis and antitumor activity of selenium-containing quinone-based triazoles possessing two redox centres, and their mechanistic insights. European Journal of Medicinal Chemistry. 122: 1-16. PMID 27341379 DOI: 10.1016/J.Ejmech.2016.06.019 |
0.557 |
|
2016 |
Namboothiri I, Nair D, Kumar T. α-Functionalization of Nitroalkenes and Its Applications in Organic Synthesis Synlett. 27: 2425-2442. DOI: 10.1055/S-0036-1588587 |
0.608 |
|
2015 |
Dutta S, Nair DK, Namboothiri IN, Wachtel E, Friedman N, Sheves M, Patchornik G. Engineered-membranes and engineered-micelles as efficient tools for purification of halorhodopsin and bacteriorhodopsin. The Analyst. 140: 204-12. PMID 25365824 DOI: 10.1039/C4An01423E |
0.571 |
|
2014 |
Nair DK, Menna-Barreto RF, da Silva Júnior EN, Mobin SM, Namboothiri IN. Chiral squaramide-catalyzed asymmetric synthesis of pyranones and pyranonaphthoquinones via cascade reactions of 1,3-dicarbonyls with Morita-Baylis-Hillman acetates of nitroalkenes. Chemical Communications (Cambridge, England). 50: 6973-6. PMID 24817645 DOI: 10.1039/c4cc02279c |
0.64 |
|
2012 |
Patchornik G, Namboothiri IN, Nair DK, Wachtel E, Cohen SR, Friedman N, Sheves M. Engineered-membranes: a novel concept for clustering of native lipid bilayers. Journal of Colloid and Interface Science. 388: 300-5. PMID 22999464 DOI: 10.1016/J.Jcis.2012.08.024 |
0.561 |
|
2012 |
Nair DK, Mobin SM, Namboothiri IN. Synthesis of imidazopyridines from the Morita-Baylis-Hillman acetates of nitroalkenes and convenient access to Alpidem and Zolpidem. Organic Letters. 14: 4580-3. PMID 22920993 DOI: 10.1021/ol3020418 |
0.646 |
|
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