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Santosh Ramdas Borkar

Researcher at Indian Institute of Technology Madras

Publications -  6
Citations -  39

Santosh Ramdas Borkar is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Fluorescence anisotropy & Micelle. The author has an hindex of 3, co-authored 6 publications receiving 35 citations.

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Study of aqueous phase aggregation of FTY720 (fingolimod hydrochloride) and its effect on DMPC liposomes using fluorescent molecular probes

TL;DR: Fluorescence intensity and lifetime decay analysis of the molecular probe 1-naphthol indicate that the interaction of FTY720 with the DMPC lipid bilayer membrane prevents partitioning of small molecules such as 1-methine to the membrane in both solid gel (SG) and liquid crystalline (LC) phases.
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Convenient synthesis of D- and L-xylo-1,2,3,4-alkane tetrols from a D-gluco-configured common building block.

TL;DR: D-gluco-configured building block derived from D-(+)-gluconolactone has served as a common chiral template for the synthesis of enantiopure D- and L-xylo- configured 1,2,3,4-alkane tetrols from a common starting point.
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A molecular level understanding of interaction between FTY720 (Fingolimod hydrochloride) and DMPC multilamellar vesicles

TL;DR: In this article, the molecular level understanding of interaction between Fingolimod hydrochloride and dimyristoylphosphatidylcholine (DMPC) multilamellar vesicles (MLVs) as a drug molecule carrier was investigated by investigating the structural changes, solubilisation effect and thermotropic phase behaviour.
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Stereoselective total synthesis of Oxylipin from open chain gluco-configured building block.

TL;DR: Total synthesis of naturally occurring Oxylipin has been achieved from open chain gluco-configured building block which is readily assembled from inexpensive and commercially available D-(+)-gluconolactone.
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Synthesis of threo- and erythro-configured trihydroxy open chain lipophilic ketones as possible anti-mycobacterial agents

TL;DR: In this article, a series of threo - and erythro -configured open-chain trihydroxy ketones was synthesized starting from l - and d -ascorbic acid respectively as the starting material, through the use of Grignard reactions for the requisite C C bond formations.