1 |
Copper(I)-Catalyzed Sandmeyer-Type S-Arylation of 1-Thiosugars with Aryldiazonium Salts under Mild Conditions, |
Venkatesh, R.; Tiwari, V.; Kandasamy, J.* |
J. Org. Chem. |
87, 11414– 11432. |
2022 |
4.3 |
2 |
Controlled reduction of activated primary and secondary amides into aldehydes with diisobutylaluminum hydride. |
Azeez, S.; Sureshbabu, P.; Sabiah, S.; Kandasamy, J.* |
Org. Biomol. Chem. |
20, 2048-2053. |
2022 |
3.8 |
3 |
Palladium-Catalyzed Reaction of Aryl Iodides and Glycal Enones: Application in the Preparation of Dapagliflozin Analogues. |
Singh, A. K.; Venkatesh, R.; Kanaujiya, V. K.; Tiwari, V.; Kandasamy, J.* |
Eur. J. Org. Chem. |
e202200023. |
2022 |
3.2 |
4 |
Synthesis of N‐Cbz Amides and Their Applications in the Transamidation Reactions at Room Temperature. |
Sureshbabu, P.; Azeez, S.; Pattanaik, K.; Sabiah, S.; Kandasamy, J.* |
Asian J. Org. Chem. |
e202200076 |
2022 |
3.3 |
5 |
Synthesis of N-Aryl α-Ketoamides, α- Ketoesters, α-Ketothioesters and Their Applications in Quinoxalinone Preparation. |
Singh, S.; Sureshbabu, P.; Sabiah, S.; Kandasamy, J.* |
Asian J. Org. Chem. |
e202200122. |
2022 |
3.3 |
6 |
An Efficient and Direct Esterification of Uronic Acids Using H2SO4-SiO2 at Room Temperature. |
Tiwari, V.; Murugan, K.; Sabiah, S.; Kandasamy, J.* |
Tetrahedron Lett. |
153852. |
2022 |
2.4 |
7 |
Multicomponent Synthesis of S-Benzyl Dithiocarbamates from para-Quinone Methides and Their Biological Evaluation for the Treatment of Alzheimer’s Di |
Venkatesh, R.; Shankar, G.; Narayanan, A. C.; Modi, G.; Sabiah, S.; Kandasamy, J.* |
J. Org. Chem. |
87, 6730–6741 |
2022 |
4.3 |
8 |
Synthesis of Glycouronamides by Transamidation Approach at Room Temperature, |
Kanaujiya, V. K.; Tiwari, V.; Pattanaik, K.; Sabiah, S.; Kandasamy, J.* |
Asian J. Org. Chem. |
e202200315. |
2022 |
3.3 |
9 |
Synthesis of 1, 3‐dicarbonyl compounds using N‐Cbz amides as an acyl source under transition metal‐free conditions at room temperature, |
Singh, S.; Kandasamy, J.* |
Asian J. Org. Chem. |
e202200416. |
2022 |
3.8 |
10 |
Synthesis of functionalized S-benzyl dithiocarbamates from diazo-compounds via multi-component reactions with carbon disulfide and secondary amines, |
Kumar, N.; Venkatesh, R.; Kandasamy, J.* |
Org. Biomol. Chem. |
20, 6766-6770. |
2022 |
3.8 |
11 |
Recent Advances and Strategies for the Transition‐Metal‐Catalyzed C−H Functionalization of N‐Nitrosoanilines. |
Chaudhary, P.; Kandasamy, J.; Macabeo, A. P. G.; Tamargo, R. J. I.; Lee, Y.R. * |
Adv. Synth. Catal. |
363, 2037-2060. |
2021 |
5.8 |
12 |
Selenium Dioxide Promoted alpha-Keto N-Acylation of Sulfoximines Under Mild Reaction Conditions, |
Baranwal, S.; Gupta, S .; Kandasamy, J.* |
Asian J. Org. Chem. |
10, 1835-1845. |
2021 |
3.3 |
13 |
Diversification of α-ketoamides via transamidation reactions with alkyl and benzyl amines at room temperature |
Singh, S.; Popuri, S.; Junaid, Q.M.; Sabiah, S.; Kandasamy J.* |
Org. Biomol. Chem. |
19, 7134-7140. |
2021 |
3.8 |
14 |
Palladium-catalyzed synthesis of α-aryl acetophenones from styryl ethers and aryl diazonium salts via regioselective Heck arylation at room temperatu |
Venkatesh, R.; Singh, A. K.; Lee, Y. R. Kandasamy, J.* |
Org. Biomol. Chem. |
19, 7832-7837. |
2021 |
3.8 |
15 |
Synthesis of photolabile group protected anomeric acetals and its application in carbohydrate synthesis with the assistance of continuous flow photo-r |
Tiwari, V.; Badavath, V. N.; Singh, A. K.; Kandasamy, J.; * |
J. Indian Chem. Soc., |
97, 227-236. |
2020 |
.28 |
16 |
tert-Butyl nitrite catalyzed synthesis of benzimidazoles from o-phenylenediamine and aldehydes at room temperature, |
Azeez, S.; Sureshbabu, P.; Sabiah, S.; Kandasamy, J.;* |
Tetrahedron Lett., |
61, 151735. |
2020 |
2.4 |
17 |
Copper catalyzed N-arylation of sulfoximines with aryldiazonium salts in the presence of DABCO under mild conditions, |
Baranwal, S.; Kandasamy, J.* |
Tetrahedron Lett., |
61, 152079. |
2020 |
2.4 |
18 |
Practical Synthesis of 3‐Functionalized Coumarins from o‐Cresols and Active Methylene Compounds under Metal and Catalyst‐Free Conditions Using t |
Chauhan, S.; Verma, P.; Kandasamy, J.; Srivastava, V. A* |
ChemistrySelect |
5, 9030-9033. |
2020 |
2.0 |
19 |
Development of Routes for the Stereoselective Preparation of β-Aryl-C-glycosides via C-1 Aryl Enones, |
Singh, A. K.; Kanaujiya, V. K.; Tiwari, V.; Sabiah, S.; Kandasamy J.* |
Org. Lett., |
22, 7650–7655. |
2020 |
6.0 |
20 |
A microbe-focused glycan array screening platform, |
Geissner, A.; Reinhardt, A.; Rademacher, C.; Johannssen, T.; Monteiro, J.; Lepenies, B.; Thépaut, M.; Fieschi, F.; Mrázková, J.; Wimmerova, M.; Schuhmacher, F.; Götze, S.; Grünstein, D.; Guo, X.; |
Proc. Natl. Acad. Sci. (USA), |
116, 1958-1967. |
2019 |
11.2 |
21 |
Regioselective Nitration of N- Alkyl Anilines using tert-Butyl Nitrite under Mild Condition, |
Chaudhary, P.; Gupta, S.; Muniyappan, N..; Sabiah, S.; Kandasamy, J.* |
J. Org. Chem. |
84, 104-119. |
2019 |
4.3 |
22 |
tert-Butyl nitrite promoted transamidation of secondary amides under metal and catalyst free conditions, |
Sureshbabu, P.; Azeez, S.; Chaudhary, P.; Kandasamy, J.* |
Org. Biomol. Chem. |
17, 845-850. |
2019 |
3.8 |
23 |
Copper-catalyzed N-arylation of sulfoximines with arylboronic acid under mild Condition, |
Gupta, S.; Baranwal,S.; Muniyappan, N..; Sabiah, S.; Kandasamy, J.* |
Synthesis , |
51, 2171-2182. |
2019 |
3.1 |
24 |
Tris(pentafluorophenyl) borane‐driven stereo- selective O‐glycosylation with glycal donors under mild condition, |
Mishra, K. B.; Kandasamy, J.* |
Asian J. Org. Chem. |
8, 549–554. |
2019 |
3.3 |
25 |
Copper-promoted dehydrogenative cross- coupling reaction of dialkyl phosphites with sulfoximines, |
Gupta, S.; Baranwal, S.; Chaudhary, P.; Kandasamy, J.* |
Org. Chem. Front., |
6, 2260-2265. |
2019 |
5.2 |
26 |
Nickel-Catalyzed Decarboxylative C–Si Bond Formation: A Regioselective Cross-Coupling Between Trialkyl Silanes and α,β-Unsaturated Carboxylic Acid |
Allam, B. K.; Azeez, S.; Kandasamy, J.;* |
Appl. Organometal. Chem., |
33, e5192. |
2019 |
4.1 |
27 |
Palladium-Catalyzed One-Pot Stereospecific Synthesis of 2-Deoxy Aryl C-Glycosides from Glycals and Anilines in the Presence of tert- Butyl Nitrite, |
Singh, A. K.; Venkatesh, R.; Kandasamy, J.* |
Synthesis, |
51, 4215-4230. |
2019 |
3.1 |
28 |
Chemo-Selective Synthesis of Aryl Ketones from Amides and Grignard Reagents via C(O)-N Bond Cleavage Under Catalyst- free Condition, |
Sureshbabu, P.; Azeez, S.; Muniyappan, N.; Sabiah, S.; Kandasamy, J.;* |
J. Org. Chem., |
84, 11823-11838. |
2019 |
4.3 |
29 |
Synthesis of photolabile protecting group (PPG) protected uronic acid building blocks: applications in carbohydrate synthesis with the assistance of a |
Tiwari, V.; Singh, A. K.; Chaudhary, P.; Seeberger, P. H.; Kandasamy J.* |
Org. Chem. Front., |
6, 3859-3863. |
2019 |
5.2 |
30 |
Molybdenumhexacarbonyl‐Mediated Imino‐Carbonylative Acylation of NH‐Sulfoximines with Aryl Iodides, |
Baranwal, S.; Gupta, S.; Sabiah, S.; Kandasamy, J.* |
Asian J. Org. Chem. |
8, 2218-2227. |
2019 |
3.3 |
31 |
tert-Butyl nitrite mediated nitrogen transfer reactions: Synthesis of benzotriazoles and azides at room temperature, |
Azeez, S.; Chaudhary, P.; Sureshbabu, P.; Sabiah, S.; Kandasamy, J.* |
Org. Biomol. Chem. |
16, 8280-8285. |
2018 |
3.8 |
32 |
Potassium persulfate promoted N-nitrosation of secondary and tertiary amines with nitromethane under mild condition, |
Azeez, S.; Chaudhary, P.; Sureshbabu, P.; Sabiah, S.; Kandasamy, J.* |
Asian J. Org. Chem. |
7, 2113-2119. |
2018 |
3.3 |
33 |
Palladium catalyzed stereocontrolled synthesis of C-aryl glycosides using glycals and arenediazonium salts at room temperature, |
Singh, A. K.; Kandasamy J.* |
Org. Biomol. Chem. |
16, 5107- 5112. |
2018 |
3.8 |
34 |
A highly efficient TEMPO mediated oxidation of sugar primary alcohols into uronic acids using 1-chloro-1,2-benziodoxol-3(1H)-one at room temperature, |
Tiwari, V.; Badavath, V. N.; Singh, A. K.; Kandasamy J.* |
Tetrahedron Lett., |
59, 2511-2514. |
2018 |
2.4 |
35 |
Tris(pentafluorophenyl)borane Promoted Stereoselective Glycosylation with Glycosyl Trichloroacetimidates under Mild Condition, |
Mishra, K.B.; Singh, A. K.; Kandasamy J.* |
J. Org. Chem. |
83, 4204-4212. |
2018 |
4.3 |
36 |
tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature, |
Chauhan, S.; Chaudhary, P.; Singh, A. K.; Verma, P.; Srivastava, V.; Kandasamy, J.* |
Tetrahedron. Lett., |
59, 272–276. |
2018 |
2.4 |
37 |
An efficient metal- free method for the denitrosation of aryl n-nitrosamines at room temperature, |
Chaudhary, P.; Korde, R.; Gupta, S.; Sureshbabu, P.; Sabiah, S.; Kandasamy, J.* |
Adv. Synth. Catal. |
360, 556–561. |
2018 |
5.8 |
38 |
Copper promoted N- alkylation of sulfoximines with alkylboronic acid under mild conditions, |
Gupta, S.; Chaudhary, P.; Muniyappan, N..; Sabiah, S.; Kandasamy, J.* |
Org. Biomol. Chem. |
15, 8493-8498. |
2017 |
3.8 |
39 |
Urea-hydrogen peroxide prompted selective and controlled oxidation of thioglycosides into Sulfoxides and Sulfones, |
Singh, A. K.; Tiwari, V.; Mishra, K. B., Gupta S.; Kandasamy, J. * |
Beilstein J. Org. Chem., |
13, 1139–1144. |
2017 |
2.8 |
40 |
Deoxygenation of tertiary amine N-oxides under metal free condition using phenylboronic acid, |
Gupta, S.; Sureshbabu, P.; Singh, A. K.; Sabiah, S.; Kandasamy, J.* |
Tetrahedron. Lett., |
58, 909- 913. |
2017 |
3.4 |
41 |
An efficient synthesis of N- nitrosamines under solvent, metal and acid free conditions using tert-butyl nitrite, |
Chaudhary, P.; Gupta, S.; Muniyappan, N.; Sabiah S.; Kandasamy, J.* |
Green Chem., |
18, 2323-2330. |
2016 |
10.1 |
42 |
A chemoselective ipso-hydroxylation of arylboronic acids using urea-hydrogen peroxide under catalyst free condition, |
Gupta, S.; Chaudhary, P.; Srivastava, V.; Kandasamy, J.* |
Tetrahedron Lett., |
57, 2506–2510. |
2016 |
2.4 |
43 |
A metal free reduction of aryl-N- nitrosamines to corresponding hydrazines using sustainable reductant thiourea dioxide, |
Chaudhary, P.; Gupta, S.; Popuri, S.; Sabiah S.; Kandasamy, J.* |
Green Chem., |
18, 6215–6221. |
2016 |
10.1 |
44 |
Bio-based green solvent for the catalyst free oxidation of arylboronic acids into phenols, |
Gupta, S.; Chaudhary, P.; Seva L.; Sabiah S.; Kandasamy, J.* |
RSC Adv., |
5, 89133–89138. |
2015 |
3.36 |
45 |
An unusual di-sulfated Iduronic acid attenuates asthmatic response in mice by interfering chemokine-heparan sulfate-mediated T cell recruitment, |
Nonaka, M.; Bao, X. Matsumura, F.; Götze, S.; Kandasamy, J.; Broide, D. H.; Nakayama, J.; Seeberger, P. H.; Fukuda M. |
Proc. Natl. Acad. Sci. (USA), |
111, 8173-8178. |
2014 |
11.2 |
46 |
Continuous Photochemical Cleavage of Linkers for Solid Phase Synthesis, |
Hurevich, M.; Kandasamy, J.; Ponnappa, B. M.; Kopetzki, D.; McQuade, T.; Seeberger, P. H. |
Org. Lett., |
16, 1794–1797. |
2014 |
6.0 |
47 |
Long- Term Nonsense Suppression Therapy Moderates MPS I-H Disease Progression, |
Gunn, G.; Dai, Y.; Du, M.; Belakhov, V.; Kandasamy, J.; Schoeb, T.; Baasov, T.; Bedwell, D. |
Mol. Genet. Metab. |
111, 374-381. |
2014 |
4.7 |
48 |
Modular automated solid phase synthesis of dermatan sulfate oligosaccharides, |
Kandasamy, J.; Schuhmacher, F.; Hahm, H.S.; Klein, J. C.; Seeberger, P. H. |
Chem. Commun. |
50, 1875-1877 |
2014 |
6.2 |
49 |
Development of generic immunoassay for the detection of a series of aminoglycosides with 6'-OH for the treatment of genetic diseases in biological sam |
Shalev, M.; Kandasamy, J.; Skalka, N.; Belakhov, V.; Rosin-Arbesfeld, R.; Baasov, T. |
J. Pharmaceut. Biomed. Anal. |
75, 33-40. |
2013 |
3.9 |
50 |
Attenuation of nonsense-mediated mRNA decay enhances in vivo nonsense suppression. |
Keeling, K.; Wang, D.; Dai, Y.; Srinivasan, M.; Chenna, B.; Clark, J.; Belakhov, V.; Kandasamy, J.; Velu, S.; Baasov, T.; Bedwell, D. |
PLoS One, |
8, e60478. |
2013 |
3.2 |
51 |
Automated solid phase synthesis of oligoarabinofuranosides, |
Kandasamy, J.; Hurevich, M.; Seeberger, P. H. |
Chem. Commun. |
49, 4453-4455. |
2013 |
6.2 |
52 |
Increased selectivity towards cytoplasmic versus mitochondrial ribosome confers improved efficiency of synthetic aminoglycosides in fixing damaged gen |
Kandasamy, J.; Glikin, D.; Shulman, E.; Shapira, K.; Shavit, M.; Belakhov, V.; Baasov, T. |
J. Med. Chem. 2012, |
55, 10630–10643. |
2012 |
7.5 |
53 |
The designer aminoglycoside NB84 significantly attenuates biochemical defects associates with MPS I-H in the Idua-W392X mouse, |
Wang, D.; Belakhov, V.; Kandasamy, J.; Baasov, T.; Li, S-C.; Li, Y-T.; Bedwell, D. M.; Keeling K. M. |
Mol. Genet. Metab., |
105, 116–125. |
2012 |
4.7 |
54 |
Repairing faulty genes by aminoglycosides: Identification of new pharmacophore with enhanced suppression of diseases-causing nonsense mutations, |
Kandasamy, J.; Glikin, D.; Belakhov, V.; Baasov, T. |
Med. Chem. Commun., |
2, 165-171 |
2011 |
3.0 |
55 |
Aminoglycosides: Redesign strategies for improved antibiotics and compounds for treatment of human genetic diseases, |
Pokrovskaya, V.; Nudelman, I.; Kandasamy, J.; Baasov, T. |
Methods in Enzymology, |
21, 437-462. |
2010 |
1.5 |
56 |
Molybdenum(VI) dichloride dioxide catalyzed oxidation of β- hydroxycarbonyls to α-bromo 1,3-dicarbonyls by N-bromosuccinimide, |
Jeyakumar, K.; Chand, D. K. |
Synthesis |
306-310. |
2009 |
3.1 |
57 |
Application of molybdenum(VI) dichloride dioxide (MoO2Cl2) in organic transformations, |
Jeyakumar, K.; Chand, D. K. |
J. Chem. Sci. |
121, 111-123 |
2009 |
1.1 |
58 |
Simple and efficient method for the oxidation of sulfides to sulfones using hydrogen peroxide and a Mo(VI) based catalyst, |
Jeyakumar, K.; Chakravarthy, R. D.; Chand, D. K. |
Catal. Commun. |
10, 1948-1941 |
2009 |
3.6 |
59 |
Molybdenum(VI)/copper(II)- An efficient bimetallic catalyst for aerobic oxidation of alcohols, |
Jeyakumar, K.; Chand, D. K. |
Open Catal. J. 2008 |
1, 6-11. |
2008 |
1.1 |
60 |
Molybdenum(VI) dichloride dioxide catalyzed synthesis of β- ketoesters by C–H insertion of ethyl diazoacetate into aldehydes, |
Jeyakumar, K.; Chand, D. K. |
Synthesis, |
1685-1687. |
2008 |
3.1 |
61 |
Ring opening reactions of epoxides catalyzed by molybdenum(VI) dichloride dioxide, |
Jeyakumar, K.; Chand, D. K. |
Synthesis |
807-819. |
2008 |
3.1 |
62 |
Copper perchlorate: Efficient acetylation catalyst under solvent free conditions, |
Jeyakumar, K.; Chand, D. K. |
J. Mol. Catal. A: Chem. |
255, 275-282. |
2006 |
5 |
63 |
Selective oxidation of sulfides to sulfoxides and sulfones at room temperature using H2O2 and a Mo(VI) salt as catalyst, |
Jeyakumar, K.; Chand, D. K. |
Tetrahedron Lett. |
47, 4573-4576 |
2006 |
2.5 |
64 |
Aerobic oxidation of benzyl alcohols by Mo (VI) compounds, |
Aerobic oxidation of benzyl alcohols by Mo (VI) compounds, |
Appl. Organometal. Chem. |
20, 840-844 |
2006 |
4.1 |
65 |
Self-assembly by ligand-exchange reactionsm, |
Chand, D. K.; Manivannan, R.; Sahoo, H. S.; Jeyakumar, K. |
Eur. J. Inorg. Chem. |
3346–3352 |
2005 |
2.5 |