B. Gopal Reddy - Publications
Affiliations: | 2003 | Indian Inst. of Technology - Kanpur |
Year | Citation | Score | |||
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2017 | Bawa A, Asefi S, Ramsey S, Arbesser-Rastburg C, Paul M, Leira F, McFarland K, Landeryou T, Reddy B, Murphy M, Daddis B, Baine D, Willison-Parry D. Mold Control and Detection In Biological Drug Substance Manufacturing Facilities: An Industry Perspective. Pda Journal of Pharmaceutical Science and Technology. PMID 28624776 DOI: 10.5731/pdajpst.2016.007351 | 0.464 | |||
2009 | Kumari N, Reddy BG, Vankar YD. Efficient and stereodivergent syntheses of D- and L-fagomines and their analogues European Journal of Organic Chemistry. 160-169. DOI: 10.1002/Ejoc.200800796 | 0.51 | |||
2005 | Reddy BG, Vankar YD. The synthesis of hybrids of D-galactose with 1-deoxynojirimycin analogues as glycosidase inhibitors Angewandte Chemie - International Edition. 44: 2001-2004. PMID 15724263 DOI: 10.1002/Anie.200462413 | 0.513 | |||
2004 | Reddy BG, Madhusudanan KP, Vankar YD. Trimethylsilylnitrate-Trimethylsilyl Azide: A Novel Reagent System for the Synthesis of 2-Deoxyglycosyl Azides from Glycals. Application in the Synthesis of 2-Deoxy-β-N-glycopeptides Journal of Organic Chemistry. 69: 2630-2633. PMID 15049677 DOI: 10.1021/Jo0354948 | 0.518 | |||
2004 | Reddy BG, Vankar YD. Trimethylsilylnitrate: a useful reagent for direct synthesis of 2-deoxy-O-glycosides from glycals $ Arkivoc. 2004. DOI: 10.3998/Ark.5550190.0005.803 | 0.497 | |||
2003 | Reddy BG, Vankar YD. A convenient synthesis of methyl N-acetyl-α-D-lividosaminide from D-glucal Tetrahedron Letters. 44: 4765-4767. DOI: 10.1016/S0040-4039(03)01044-X | 0.497 | |||
2001 | Kumareswaran R, Reddy B, Vankar Y. Nafion-H-catalyzed Mukaiyama aldol condensations and hetero Diels–Alder reactions using aldehydes and imines. Part 15: General synthetic methods Tetrahedron Letters. 42: 7493-7495. DOI: 10.1016/S0040-4039(01)01592-1 | 0.636 | |||
2000 | Reddy B, Kumareswaran R, Vankar Y. Indium trichloride: a useful catalyst for ionic Diels–Alder reactions Tetrahedron Letters. 41: 10333-10336. DOI: 10.1016/S0040-4039(00)01857-8 | 0.625 | |||
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