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A. P. John Pal
Researcher at Indian Institute of Technology Kanpur
Publications - 9
Citations - 188
A. P. John Pal is an academic researcher from Indian Institute of Technology Kanpur. The author has contributed to research in topics: Glycosylation & Dihydroxylation. The author has an hindex of 7, co-authored 9 publications receiving 178 citations.
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Ceric Ammonium Nitrate-Catalyzed Azidation of 1,2-Anhydro Sugars: Application in the Synthesis of Structurally Diverse Sugar-Derived Morpholine 1,2,3-Triazoles and 1,4-Oxazin-2-ones
TL;DR: Various 1,2-anhydro sugars produced 2-hydroxy-1-azido sugars in good yields which, in turn, were converted to structurally diverse sugar-derived morpholine triazoles and sugar oxazin-2-ones.
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Synthesis of hybrids of D-glucose and D-galactose with pyrrolidine-based iminosugars as glycosidase inhibitors
Venkata Ramana Doddi,Hari Prasad Kokatla,A. P. John Pal,Ranjan Kumar Basak,Yashwant D. Vankar +4 more
TL;DR: Sugar-iminosugar hybrid molecules made up of D-glucose and D-galactose with pyrrolidine-based iminosugars are synthesized from glycal epoxides and found to be moderate glycosidase inhibitors.
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Total synthesis of (+)-pericosine B and (+)-pericosine C and their enantiomers by using the Baylis–Hillman reaction and ring-closing metathesis as key steps
TL;DR: In this article, a simple and divergent route for the total synthesis of pericosine B and C and their enantiomers from d -ribose by using the Baylis-Hillman reaction and ring-closing metathesis reactions as key steps is described.
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Synthesis of aminocyclitols and trihydroxylated indolizidinone from a D-mannitol-derived common building block
TL;DR: In this paper, the synthesis of 4-amino-4-deoxy-muco-quercitol and trihydroxylated indolizidinone 38 from D-mannitol is described using ring-closing metathesis and diastereoselective dihydylation as the key steps.
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Azidation of anomeric nitro sugars: application in the synthesis of spiroaminals as glycosidase inhibitors
TL;DR: 6,5-Fused sugar-derived spiroaminals have been synthesized from the azido esters obtained via the nucleophilic substitution reactions of unstable Michael adducts derived from 1-nitro sugars.