Perali Ramu Sridhar - Publications

2007- University of Hyderabad, Hyderabad, Telangana, India 
Carbohydrate chemistry, glyco-chemistry

16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  1
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  0.6
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  0.6
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  1
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  0.88
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  1
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  0.88
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  0.88
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  0.88
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  0.64
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  0.64
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  0.88
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  0.64
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  0.64
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  0.64
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  0.64
Show low-probability matches.