Year |
Citation |
Score |
2023 |
Santhanam V, Modi P, Mishra UK, Jahan I, Ramesh NG, Deep S. Rational design and synthesis of novel triazole- and tetrazole-fused iminosugars as potential inhibitors of amyotrophic lateral sclerosis (ALS) linked SOD1 aggregation. International Journal of Biological Macromolecules. 126900. PMID 37714236 DOI: 10.1016/j.ijbiomac.2023.126900 |
0.68 |
|
2022 |
Mishra UK, Sanghvi YS, Abhiraj R, Sampathkumar SG, Ramesh NG. An expeditious synthesis of novel DNA nucleobase mimics of (+)-anisomycin. Carbohydrate Research. 520: 108645. PMID 35964481 DOI: 10.1016/j.carres.2022.108645 |
0.378 |
|
2021 |
Ramesh NG. From Glycals to Nitrogen Heterocycles and Carbocycles via "Cleavage-Intramolecular Recombination Strategy". Chemical Record (New York, N.Y.). 21: 2930-2957. PMID 34472196 DOI: 10.1002/tcr.202100187 |
0.534 |
|
2020 |
Salunke RV, Mishra PK, Sanghvi YS, Ramesh NG. Synthesis of novel homoazanucleosides and their peptidyl analogs. Organic & Biomolecular Chemistry. 18: 5639-5651. PMID 32724966 DOI: 10.1039/d0ob01046d |
0.398 |
|
2020 |
Harit VK, Ramesh NG. A common strategy towards the synthesis of 1,4-dideoxy-1,4-imino-l-xylitol, deacetyl (+)-anisomycin and amino-substituted piperidine iminosugars. Carbohydrate Research. 492: 107988. PMID 32387805 DOI: 10.1016/j.carres.2020.107988 |
0.414 |
|
2020 |
Mishra UK, Ramesh NG. A glycal based approach to the synthesis of (+)-bulgecinine, 3-hydroxy-2,5-dihydroxymethylpyrrolidine and 2-oxapyrrolizidin-3-one. Carbohydrate Research. 489: 107931. PMID 32088502 DOI: 10.1016/j.carres.2020.107931 |
0.359 |
|
2019 |
Harit VK, Ramesh NG. Ring closing metathesis (RCM) approach to the synthesis of conduramine B-2, ent-conduramine F-2, aminocyclopentitol and trihydroxyazepane. Organic & Biomolecular Chemistry. 17: 5951-5961. PMID 31166343 DOI: 10.1039/c9ob01010f |
0.415 |
|
2019 |
Santhanam V, Pant P, Jayaram B, Ramesh NG. Design, synthesis and glycosidase inhibition studies of novel triazole fused iminocyclitol-δ-lactams. Organic & Biomolecular Chemistry. 17: 1130-1140. PMID 30633287 DOI: 10.1039/C8Ob03084G |
0.703 |
|
2019 |
Iio K, Ramesh NG, Okajima A, Higuchi K, Fujioka H, Akai S, Kita Y. An efficient synthesis of peri-hydroxy aromatic compounds via a strong-base-induced. The Journal of Organic Chemistry. 65: 89-95. PMID 10813900 DOI: 10.1021/jo990649q |
0.478 |
|
2016 |
Harit VK, Ramesh NG. A Chiron Approach to Diversity-Oriented Synthesis of Aminocyclitols, (-)-Conduramine F-4 and Polyhydroxyaminoazepanes from a Common Precursor. The Journal of Organic Chemistry. 81: 11574-11586. PMID 27806198 DOI: 10.1021/acs.joc.6b01790 |
0.415 |
|
2016 |
Salunke RV, Ramesh NG. A Concise Total Synthesis of the Stereoisomers of (–)‐Pochonicine European Journal of Organic Chemistry. 2016: 654-657. DOI: 10.1002/Ejoc.201501413 |
0.587 |
|
2014 |
Ramesh NG. Applications of 2-C-Formyl-Glycals in Organic Synthesis† European Journal of Organic Chemistry. 2014: 689-707. DOI: 10.1002/Ejoc.201301176 |
0.593 |
|
2013 |
Ganesan M, Salunke RV, Singh N, Ramesh NG. Protecting group directed diversity during Mitsunobu cyclization of a carbohydrate derived diamino triol. Synthesis of novel bridged bicyclic and six-membered iminocyclitols. Organic & Biomolecular Chemistry. 11: 599-611. PMID 23207451 DOI: 10.1039/c2ob27000e |
0.389 |
|
2012 |
Martínez-Montero S, Fernández S, Sanghvi YS, Chattopadhyaya J, Ganesan M, Ramesh NG, Gotor V, Ferrero M. Design and divergent synthesis of aza nucleosides from a chiral imino sugar. The Journal of Organic Chemistry. 77: 4671-8. PMID 22551299 DOI: 10.1021/Jo3004452 |
0.352 |
|
2011 |
Nagaraj P, Ramesh NG. HSAB-driven regioselectivity difference in the Lewis-acid catalyzed reactions of 2-C-substituted glycals with sulfur and oxygen nucleophiles: Direct versus allylic substitution Tetrahedron. 67: 9322-9328. DOI: 10.1016/J.Tet.2011.09.122 |
0.603 |
|
2010 |
Ganesan M, Madhukarrao RV, Ramesh NG. Design and synthesis of new amino-modified iminocyclitols: selective inhibitors of alpha-galactosidase. Organic & Biomolecular Chemistry. 8: 1527-30. PMID 20237662 DOI: 10.1039/b926123k |
0.327 |
|
2009 |
Nagaraj P, Ramesh NG. Direct Ferrier rearrangement on unactivated glycals catalyzed by indium(III) chloride Tetrahedron Letters. 50: 3970-3973. DOI: 10.1016/J.Tetlet.2009.04.084 |
0.595 |
|
2007 |
Kumar V, Ramesh NG. A versatile strategy for the synthesis of N-linked glycoamino acids from glycals Organic and Biomolecular Chemistry. 5: 3847-3858. PMID 18004466 DOI: 10.1039/B712841J |
0.575 |
|
2006 |
Kumar V, Ramesh NG. Iodine catalyzed one-pot diamination of glycals with chloramine-T: a new approach to 2-amino-β-glycosylamines for applications in N-glycopeptide synthesis Chemical Communications. 4952-4. PMID 17136258 DOI: 10.1039/B612151A |
0.526 |
|
2003 |
Ramesh NG, Balasubramanian KK. 2‐C‐Formyl Glycals: Emerging Chiral Synthons in Organic Synthesis European Journal of Organic Chemistry. 2003: 4477-4487. DOI: 10.1002/Ejoc.200300383 |
0.727 |
|
2002 |
Ramesh NG, Heijne EH, Klunder AJH, Zwanenburg B. An efficient regioselective halogenation of 5-amino-endo-tricyclo[5.2.1.02,6]deca-4,8-dien-3-ones Tetrahedron. 58: 1361-1368. DOI: 10.1016/S0040-4020(01)01228-5 |
0.629 |
|
2001 |
Arisawa M, Ramesh NG, Nakajima M, Tohma H, Kita Y. Hypervalent iodine(III)-induced intramolecular cyclization of alpha-(aryl)alkyl-beta-dicarbonyl compounds: a convenient synthesis of benzannulated and spirobenzannulated compounds. The Journal of Organic Chemistry. 66: 59-65. PMID 11429930 DOI: 10.1021/jo000953f |
0.398 |
|
1999 |
Ramesh NG, Klunder AJ, Zwanenburg B. Enantioselective Synthesis of 4-Acetylaminocyclopent-2-en-1-ols from Tricyclo[5.2.1.0(2,6)]decenyl Enaminones. Precursors for 5'-Norcarbocyclic Nucleosides and Related Antiviral Compounds. The Journal of Organic Chemistry. 64: 3635-3641. PMID 11674491 DOI: 10.1021/Jo982498H |
0.51 |
|
1998 |
Ramesh NG, Heijne EH, Klunder AJH, Zwanenburg B. An effective regioselective electrophilic halogenation of tricyclo[5.2.1.02,6]decenyl enaminones Tetrahedron Letters. 39: 3295-3298. DOI: 10.1016/S0040-4039(98)00474-2 |
0.6 |
|
1998 |
Ramesh NG, Klunder AJH, Zwanenburg B. Enantioselective synthesis of 4-aminocyclopent-2-ene-1-one from tricyclo[5.2.1.02,6]decenyl enaminones Tetrahedron Letters. 39: 1429-1432. DOI: 10.1016/S0040-4039(97)10820-6 |
0.639 |
|
1995 |
Ramesh NG, Balasubramanian KK. Mitsunobu reaction of 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-hydroxymethyl-hex-1-enitols and 1,5-anhydro-2-deoxy-4,6-O-protected-hex-1-enitols. A novel method for the synthesis of 2-C-methylene glycosides and an useful alternative to Ferrier rearrangement Tetrahedron. 51: 255-272. DOI: 10.1016/0040-4020(94)00939-R |
0.721 |
|
1992 |
Ramesh NG, Balasubramanian KK. Reaction of 2,3-unsaturated aryl glycosides with lewis acids : a convenient entry to C-aryl glycosides Tetrahedron Letters. 33: 3061-3064. DOI: 10.1016/S0040-4039(00)79600-6 |
0.727 |
|
1991 |
Ramesh NG, Balasubramanian KK. Vilsmeier-haack reactoin of glycals-a short route to C-2-formyl glycals☆ Tetrahedron Letters. 32: 3875-3878. DOI: 10.1016/S0040-4039(00)79402-0 |
0.556 |
|
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