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Synthesis of novel l-rhamnose derived acyclic C-nucleosides with substituted 1,2,3-triazole core as potent sodium-glucose co-transporter (SGLT) inhibitors.
Bioorg Med Chem Lett. 2014 Mar 15;24(6):1528-31. doi: 10.1016/j.bmcl.2014.01.077. Epub 2014 Feb 6.
Bioorg Med Chem Lett. 2014.
PMID: 24556379
Synthesis of L-rhamnose derived chiral bicyclic triazoles as novel sodium-glucose transporter (SGLT) inhibitors.
Putapatri SR, Kanwal A, Sridhar B, Banerjee SK, Kantevari S.
Putapatri SR, et al.
Org Biomol Chem. 2014 Nov 14;12(42):8415-21. doi: 10.1039/c4ob01319k.
Org Biomol Chem. 2014.
PMID: 25175761
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Correction: Synthesis of l-rhamnose derived chiral bicyclic triazoles as novel sodium-glucose transporter (SGLT) inhibitors.
Putapatri SR, Kanwal A, Sridhar B, Banerjee SK, Kantevari S.
Putapatri SR, et al.
Org Biomol Chem. 2017 Jul 19;15(28):6057. doi: 10.1039/c7ob90112g.
Org Biomol Chem. 2017.
PMID: 28686256
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Facile diversity-oriented synthesis and antitubercular evaluation of novel aryl and heteroaryl tethered pyridines and dihydro-6H-quinolin-5-ones derived via variants of the Bohlmann-Rahtz Reaction.
Kantevari S, Patpi SR, Addla D, Putapatri SR, Sridhar B, Yogeeswari P, Sriram D.
Kantevari S, et al. Among authors: putapatri sr.
ACS Comb Sci. 2011 Jul 11;13(4):427-35. doi: 10.1021/co2000604. Epub 2011 Jun 23.
ACS Comb Sci. 2011.
PMID: 21699150
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