Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Murugesan Sasikumar"'
Autor:
Duraivelu, Hemanand, Dhamodharan, Udaya Suriya Rajkumar, Udayaraju, Pamula, Prakash, S. Jaya, Murugesan, Sasikumar
Publikováno v:
Journal of Information Technology Management (JITM); 2024, Vol. 16 Issue 1, p135-148, 14p
Publikováno v:
New Journal of Chemistry. 43:15052-15056
Novel dendrimer supported spiroborate catalysts 2 and 3 have been synthesized using a click reaction as a key step. The catalytic efficiency of the catalysts have been verified with reduction of (E)-O-benzyl oxime 13 as a model substrate. Catalyst 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e354c1bf331c8706ab5429f63c5fe473
https://doi.org/10.1039/c9nj03217g
https://doi.org/10.1039/c9nj03217g
Autor:
Shirish P. Deshmukh, Mohammad Mujahid, Murugan Muthukrishnan, Murugesan Sasikumar, Prashant Mujumdar
Publikováno v:
Tetrahedron: Asymmetry. 28:983-986
A simple and efficient synthesis of the opioid analgesic agent ( R )-phenampromide with high enantiopurity (>99% ee) via the formation of an aziridinium ion as a key step using commercially available starting material is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce036fe4d729365d79c1a4240eeeb5a2
https://doi.org/10.1016/j.tetasy.2017.06.001
https://doi.org/10.1016/j.tetasy.2017.06.001
Autor:
Murugesan Sasikumar, Murugan Muthukrishnan, Sunita S. Kunte, Jambu Subramanian, Viswanadh Nalla, Mohammad Mujahid
Publikováno v:
New Journal of Chemistry. 41:824-829
A concise and efficient enantioselective synthesis of both enantiomers of bepridil, a calcium channel blocker, is reported. Jacobsen's hydrolytic kinetic resolution method was utilized to resolve racemic 2-(isobutoxymethyl)oxirane. The incorporation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8847a7a1acd52bec24b5500a73b4ad4
https://doi.org/10.1039/c6nj02928k
https://doi.org/10.1039/c6nj02928k
Autor:
Savio, Max1, Murugesan, Sasikumar2
Publikováno v:
International Journal on Electrical Engineering & Informatics. Mar2014, Vol. 6 Issue 1, p129-143. 15p.
Publikováno v:
Tetrahedron Letters. 57:861-863
An alternate synthesis of (R)-2-benzylmorpholine 1, an appetite suppressant agent has been accomplished starting from readily available trans-cinnamyl alcohol employing Sharpless asymmetric epoxidation strategy as a key step, with an overall yield of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66e361c64e32c89e6173a144bac4158a
https://doi.org/10.1016/j.tetlet.2016.01.032
https://doi.org/10.1016/j.tetlet.2016.01.032
Publikováno v:
Synthesis. 46:1751-1756
An alternative highly enantioselective synthesis of the anti-Parkinson agent safinamide from simple, commercially available, starting materials is described. The protocol might also be useful in the synthesis of structural variants of safinamide, suc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a53389f552292ba6f354b44e9b4f6f21
https://doi.org/10.1055/s-0033-1341104
https://doi.org/10.1055/s-0033-1341104
Autor:
Mohammad Mujahid, Sunita S. Kunte, Prashant Mujumdar, Murugan Muthukrishnan, Murugesan Sasikumar
Publikováno v:
Tetrahedron: Asymmetry. 23:1512-1515
A simple and efficient synthesis of levetiracetam has been achieved with high enantiopurity (>99%) starting from commercially available benzyl glycidyl ether. The method is amenable for industrial scale-up.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::689e6611a2ceeeec94ad131c09573aaa
https://doi.org/10.1016/j.tetasy.2012.10.006
https://doi.org/10.1016/j.tetasy.2012.10.006
Autor:
Murugesan Sasikumar, Milind D. Nikalje
Publikováno v:
Synthetic Communications. 42:3061-3067
A refinement in the synthetic strategy for (S)-dapoxetine 1 is described. The key features of synthetic strategy include (a) a Sharpless asymmetric epoxidation reaction and regioselective reductive ring opening of a 2,3-epoxy alcohol to elaborate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e0ccfe0207c7d6a10c0a6b4b3dacdc6
https://doi.org/10.1080/00397911.2011.575522
https://doi.org/10.1080/00397911.2011.575522
Publikováno v:
Tetrahedron: Asymmetry. 22:1353-1357
An efficient asymmetric synthesis of the new antiepileptic drug, Lacosamide is described in high enantiopurity (>98% ee), using Jacobsen’s hydrolytic kinetic resolution strategy as a key step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79680bb47548415586816ec08db391b3
https://doi.org/10.1016/j.tetasy.2011.07.024
https://doi.org/10.1016/j.tetasy.2011.07.024