Year |
Citation |
Score |
2022 |
Sridhar PR, Ali I, Lakshmi MVK. Synthesis of Hexenuloses and a Library of Disaccharides Possessing 3-oxo-glycal Unit. The Journal of Organic Chemistry. PMID 35772022 DOI: 10.1021/acs.joc.2c00663 |
0.824 |
|
2019 |
Sridhar PR, Reddy VD, Suresh M, Reddy NM, Kumar KS. Synthesis of Carbocyclic Nucleosides (+)-Neplanocin A, (+)-Aristeromycin and 4'-epi-(+)-Aristeromycin from D-Fructose Letters in Organic Chemistry. 16: 750-758. DOI: 10.2174/1570178615666181023145502 |
0.517 |
|
2019 |
Sridhar PR, Rao BU, Reddy GM. Synthesis of Carbon-Branched Sugars Involving an Unprecedented 1,5- or 1,6-Alkyl Transposition Reaction European Journal of Organic Chemistry. 2019: 4752-4756. DOI: 10.1002/Ejoc.201900752 |
0.461 |
|
2018 |
Sridhar PR, Venkatesh BC, Kalesha S, Sudharani C. The first total synthesis of gobichelin B: a mixed-ligand siderophore of Streptomyces sp. NRRL F-4415. Organic & Biomolecular Chemistry. PMID 29565443 DOI: 10.1039/C8Ob00263K |
0.742 |
|
2016 |
Reddy GM, Maheswara Rao BU, Sridhar PR. Stereoselective Synthesis of 2-(β-C-Glycosyl)glycals: Access to Unusual β-C-Glycosides from 3-Deoxyglycals. The Journal of Organic Chemistry. 81: 2782-93. PMID 26926318 DOI: 10.1021/Acs.Joc.5B02879 |
0.802 |
|
2016 |
Ramakrishna B, Sudharani C, Sridhar PR. Synthesis of β-C-Glycosyl Amino Acids by Ring Opening of Donor-Acceptor Spiro-cyclopropanecarboxylated Sugars Israel Journal of Chemistry. DOI: 10.1002/Ijch.201500087 |
0.775 |
|
2016 |
Ganesh V, Sridhar PR, Chandrasekaran S. Synthetic Applications of Carbohydrate-derived Donor-Acceptor Cyclopropanes Israel Journal of Chemistry. DOI: 10.1002/Ijch.201500086 |
0.842 |
|
2015 |
Ramakrishna B, Sridhar PR. Stereoselective synthesis of 1,6-dioxaspirolactones from spiro-cyclopropanecarboxylated sugars: Total synthesis of dihydro-pyrenolide D Rsc Advances. 5: 8142-8145. DOI: 10.1039/C4Ra16753H |
0.798 |
|
2014 |
Reddy GM, Sridhar PR. The first stereoselective total synthesis of neosemburin and isoneosemburin. Organic & Biomolecular Chemistry. 12: 8408-14. PMID 25072802 DOI: 10.1039/C4Ob01239A |
0.632 |
|
2014 |
Venukumar P, Sudharani C, Sridhar PR. A one-pot septanoside formation and glycosylation of acyclic dithioacetals derived from 1,2-cyclopropanated sugars. Chemical Communications (Cambridge, England). 50: 2218-21. PMID 24435224 DOI: 10.1039/C3Cc49116A |
0.787 |
|
2014 |
Seshadri K, Sridhar PR. Synthesis of C2-Methylene Glycitols from 1,2-Cyclopropanated Sugars: En Route to Iminosugar Analogues Synthesis (Germany). 46: 923-932. DOI: 10.1055/S-0033-1340617 |
0.854 |
|
2014 |
Sudharani C, Venukumar P, Sridhar PR. Stereoselective Synthesis ofC-2-Methylene andC-2-Methyl α- and β-C-Glycosides from 2-C-Branched Glycals: Formal Total Synthesis of (-)-Brevisamide European Journal of Organic Chemistry. 2014: 8085-8093. DOI: 10.1002/Ejoc.201403062 |
0.778 |
|
2014 |
Seshadri K, Sridhar PR. ChemInform Abstract: Synthesis of C2-Methylene Glycitols from 1,2-Cyclopropanated Sugars: En Route to Iminosugar Analogues. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201440198 |
0.853 |
|
2014 |
Ramakrishna B, Sridhar PR. ChemInform Abstract: Ring-Contraction vs Ring-Expansion Reactions of Spiro-Cyclopropanecarboxylated Sugars. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201405205 |
0.801 |
|
2013 |
Ramakrishna B, Sridhar PR. Ring-contraction vs ring-expansion reactions of spiro- cyclopropanecarboxylated sugars Organic Letters. 15: 4474-4477. PMID 23964753 DOI: 10.1021/Ol402021E |
0.81 |
|
2013 |
Reddy GM, Sridhar PR. Stereoselective Construction of 2,8-Dioxabicyclo[3.3.1]nonane/nonene Systems from 3-C-Branched Glycals European Journal of Organic Chemistry. 2014: 1496-1504. DOI: 10.1002/Ejoc.201301665 |
0.575 |
|
2013 |
Sridhar PR, Reddy GM, Seshadri K. ChemInform Abstract: Stereoselective Synthesis of cis-Fused Perhydrofuro[2,3-b]furan Derivatives from Sugar-Derived Allyl Vinyl Ethers. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201312092 |
0.821 |
|
2012 |
Sridhar PR, Venukumar P. A ring expansion-glycosylation strategy toward the synthesis of septano-oligosaccharides. Organic Letters. 14: 5558-61. PMID 23072521 DOI: 10.1021/Ol302677Z |
0.839 |
|
2012 |
Sridhar PR, Seshadri K, Reddy GM. Stereoselective synthesis of sugar fused β-disubstituted γ-butyro-lactones: C-spiro-glycosides from 1,2-cyclopropanecarboxylated sugars. Chemical Communications (Cambridge, England). 48: 756-8. PMID 22134500 DOI: 10.1039/C1Cc16417A |
0.869 |
|
2012 |
Sridhar PR, Sudharani C. Stereoselective synthesis of C-2-methylene and C-2-methyl-C-glycosides by Claisen rearrangement of 2-vinyloxymethyl glycals Rsc Advances. 2: 8596. DOI: 10.1039/C2Ra21505E |
0.806 |
|
2012 |
Sridhar PR, Reddy GM, Seshadri K. Stereoselective synthesis of cis-fused perhydrofuro[2,3-b]furan derivatives from sugar-derived allyl vinyl ethers European Journal of Organic Chemistry. 6228-6235. DOI: 10.1002/Ejoc.201200898 |
0.831 |
|
2009 |
Sridhar PR, Kumar PV, Seshadri K, Satyavathi R. Synthesis of 2-C-branched oligo(glyco-amino acid)s (OGAAs) by ring opening of 1,2-cyclopropanecarboxylated sugar donors. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 7526-9. PMID 19585644 DOI: 10.1002/Chem.200901022 |
0.859 |
|
2007 |
Sivapriya K, Suguna P, Shubashree S, Sridhar PR, Chandrasekaran S. Novel chalcogenides of thymidine and uridine: synthesis, properties and applications. Carbohydrate Research. 342: 1151-8. PMID 17397814 DOI: 10.1016/J.Carres.2007.02.035 |
0.783 |
|
2007 |
Haveli SD, Sridhar PR, Suguna P, Chandrasekaran S. Efficient synthesis of fused perhydrofuro[2,3-b]pyrans (and furans) by ring opening of 1,2-cyclopropanated sugar derivatives. Organic Letters. 9: 1331-4. PMID 17335228 DOI: 10.1021/Ol070177Z |
0.762 |
|
2006 |
Ghosh AK, Sridhar PR, Leshchenko S, Hussain AK, Li J, Kovalevsky AY, Walters DE, Wedekind JE, Grum-Tokars V, Das D, Koh Y, Maeda K, Gatanaga H, Weber IT, Mitsuya H. Structure-based design of novel HIV-1 protease inhibitors to combat drug resistance. Journal of Medicinal Chemistry. 49: 5252-61. PMID 16913714 DOI: 10.1021/Jm060561M |
0.35 |
|
2005 |
Sridhar PR, Saravanan V, Chandrasekaran S. Chemistry of tetrathiomolybdate and tetraselenotungstate: Applications in carbohydrate chemistry Pure and Applied Chemistry. 77: 145-153. DOI: 10.1351/Pac200577010145 |
0.717 |
|
2005 |
Sridhar PR, Prabhu KR, Chandrasekaran S. Synthesis of Thioglycosides by Tetrathiomolybdate-Mediated Michael Additions of Masked Thiolates. Cheminform. 36. DOI: 10.1002/CHIN.200514195 |
0.663 |
|
2004 |
Sridhar PR, Ashalu KC, Chandrasekaran S. Efficient methodology for the synthesis of 2-C-branched glyco-amino acids by ring opening of 1,2-cyclopropanecarboxylated sugars. Organic Letters. 6: 1777-9. PMID 15151412 DOI: 10.1021/Ol049467V |
0.806 |
|
2004 |
Sridhar PR. Chemistry of tetrathiomolybdate and tetraselenotungstate: Applications in carbohydrate and peptide chemistry Synlett. 2004: 744-745. DOI: 10.1055/S-2004-817757 |
0.452 |
|
2004 |
Sridhar P, Prabhu K, Chandrasekaran S. Synthesis of Thioglycosides by Tetrathiomolybdate-Mediated Michael Additions of Masked Thiolates European Journal of Organic Chemistry. 2004: 4809-4815. DOI: 10.1002/Ejoc.200400360 |
0.822 |
|
2003 |
Sridhar PR, Prabhu KR, Chandrasekaran S. Selective reduction of anomeric azides to amines with tetrathiomolybdate: synthesis of beta-D-glycosylamines. The Journal of Organic Chemistry. 68: 5261-4. PMID 12816487 DOI: 10.1021/Jo0266947 |
0.78 |
|
2002 |
Devan N, Sridhar PR, Prabhu KR, Chandrasekaran S. Tetrathiomolybdate assisted epoxide ring opening with masked thiolates and selenoates: multistep reactions in one pot. The Journal of Organic Chemistry. 67: 9417-20. PMID 12492347 DOI: 10.1021/Jo0263418 |
0.775 |
|
2002 |
Sridhar PR, Chandrasekaran S. Propargyloxycarbonyl (Poc) as a protective group for the hydroxyl function in carbohydrate synthesis. Organic Letters. 4: 4731-3. PMID 12489973 DOI: 10.1021/Ol027220X |
0.7 |
|
2002 |
Sridhar PR, Chandrasekaran S. Propargyloxycarbonyl (Poc) as a Protective Group for the Hydroxyl Function in Carbohydrate Synthesis Organic Letters. 4: 4731-4733. DOI: 10.1021/ol027220x |
0.665 |
|
Low-probability matches (unlikely to be authored by this person) |
2014 |
Reddy GM, Sridhar PR. ChemInform Abstract: Stereoselective Construction of 2,8-Dioxabicyclo[3.3.1]nonane/nonene Systems from 3-C-Branched Glycals. Cheminform. 45: no-no. DOI: 10.1002/CHIN.201449033 |
0.288 |
|
2023 |
Shankar B, Venkatesh BC, Sridhar PR. Efforts toward the first total synthesis of a mixed-ligand siderophore: Gobichelin-A. Journal of Peptide Science : An Official Publication of the European Peptide Society. e3525. PMID 37230473 DOI: 10.1002/psc.3525 |
0.268 |
|
2016 |
Dhanarajan G, Rangarajan V, Sridhar PR, Sen R. Development and Scale-up of an Efficient and Green Process for HPLC Purification of Antimicrobial Homologues of Commercially Important Microbial Lipopeptides Acs Sustainable Chemistry & Engineering. 4: 6638-6646. DOI: 10.1021/Acssuschemeng.6B01498 |
0.252 |
|
2016 |
Ganesh V, Sridhar PR, Chandrasekaran S. ChemInform Abstract: Synthetic Applications of Carbohydrate-Derived Donor-Acceptor Cyclopropanes Cheminform. 47. DOI: 10.1002/CHIN.201636230 |
0.249 |
|
2010 |
Woodward R, Yi W, Li L, Zhao G, Eguchi H, Sridhar PR, Guo H, Song JK, Motari E, Cai L, Kelleher P, Liu X, Han W, Zhang W, Ding Y, et al. In vitro bacterial polysaccharide biosynthesis: Defining the functions of Wzy and Wzz Nature Chemical Biology. 6: 418-423. PMID 20418877 DOI: 10.1038/Nchembio.351 |
0.219 |
|
2010 |
Reddy NP, Aparoy P, Reddy TC, Achari C, Sridhar PR, Reddanna P. Design, synthesis, and biological evaluation of prenylated chalcones as 5-LOX inhibitors. Bioorganic & Medicinal Chemistry. 18: 5807-15. PMID 20667741 DOI: 10.1016/j.bmc.2010.06.107 |
0.193 |
|
2012 |
Reddy NP, Chandramohan Reddy T, Aparoy P, Achari C, Sridhar PR, Reddanna P. Structure based drug design, synthesis and evaluation of 4-(benzyloxy)-1-phenylbut-2-yn-1-ol derivatives as 5-lipoxygenase inhibitors. European Journal of Medicinal Chemistry. 47: 351-9. PMID 22118829 DOI: 10.1016/j.ejmech.2011.11.003 |
0.111 |
|
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