Damodara N. Reddy

Affiliations: 
2013 Indian Institute of Science Bangalore 
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"Damodara Reddy"
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Meena R, Shekhar S, Ansari SB, et al. (2023) Metal-free sp2-C7-H Borylation of Tryptophan Containing Peptides and Late-stage Modification. Chemistry, An Asian Journal. e202300638
Lal J, Kaul G, Akhir A, et al. (2023) β-Turn editing in Gramicidin S: Activity impact on replacing proline α-carbon with stereodynamic nitrogen. Bioorganic Chemistry. 138: 106641
Lal J, Prajapati G, Meena R, et al. (2022) Influence of Proline Chirality on Neighbouring Azaproline Residue Stereodynamic Nitrogen Preorganization. Chemistry, An Asian Journal
Tumminakatti S, Reddy DN, Prabhakaran EN. (2015) Exploring the consequences of a representative "disallowed" conformation of Aib on a 310 -helical fold. Biopolymers. 104: 21-36
Reddy DN, Prabhakaran EN. (2014) Steric and electronic interactions controlling the cis/trans isomer equilibrium at X-pro tertiary amide motifs in solution. Biopolymers. 101: 66-77
Tumminakatti S, Reddy DN, Lakshmi AN, et al. (2014) Synthesis of 5,6-dihydro-4H-1,3-thiazine containing peptide mimics from N-(3-hydroxypropyl)thioamides and epimerization studies Tetrahedron Letters. 4731-4735
Reddy DN, George G, Prabhakaran EN. (2013) Crystal-structure analysis of cis-X-Pro-containing peptidomimetics: understanding the steric interactions at cis X-Pro amide bonds. Angewandte Chemie (International Ed. in English). 52: 3935-9
Reddy DN, Thirupathi R, Tumminakatti S, et al. (2012) A method for stabilizing the cis prolyl peptide bond: Influence of an unusual n→π * interaction in 1,3-oxazine and 1,3-thiazine containing peptidomimetics Tetrahedron Letters. 53: 4413-4417
Reddy DN, Thirupathi R, Prabhakaran EN. (2011) Accessing the disallowed conformations of peptides employing amide-to-imidate modification. Chemical Communications (Cambridge, England). 47: 9417-9
Reddy DN, Prabhakaran EN. (2011) Synthesis and isolation of 5,6-dihydro-4H-1,3-oxazine hydrobromides by autocyclization of N-(3-bromopropyl)amides. The Journal of Organic Chemistry. 76: 680-3
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