Dr. Rashmi Roy

Qualification : Ph.D. (IIT, Kanpur)

Details of Educational Qualification:

Course Specialization Group College Name/University Year of Passing
Ph.D. Organic Chemistry Organic Chemistry Indian Institute of Technology, Kanpur 2015
M.Sc. Organic chemistry Applied Chemistry Bengal Engineering & Science University, Shibpur 2006
B.Sc. Chemistry, Physics & Mathematics B.Sc. University of Calcutta 2004


List of Publications

S.No Title of the Paper Full Details of Journal Name / Conference Name, Volume number, page number, Date
1 “Neoglycolipids as Glycosphingolipid Surrogates for Protein Binding Studies Using Nanodiscs and Native Mass Spectrometry” Chem. 2020, 92, 20, 14189–14196. (Citation : 3)
2 “Scope and advances in the catalytic propargylic substitution reaction” RSC Adv., 2018, 8, 31129-31193. (Google scholar citation: 62)
3 “AuCl3 and AuCl3-Phenylacetylene catalyzed glycosylations using glycosyl trichloroacetimidates” Eur. J. Org. Chem, 2015, 18, 4000–4005. (Google scholar citation: 17)
4 “Gold (III) Chloride and Phenylacetylene: A Catalyst System for the Ferrier Rearrangement, and O-Glycosylation of 1-O-Acetyl Sugars as GlycosylDonors” Eur. J. Org. Chem. 2014, 25, 5564−5573. (Google Scholar citation: 25)
5 “Synthesis of isofagomine and some new azasugars as glycosidase inhibitors from D- mannitol derivednitroolefins” Tetrahedron: Asymmetry 2013, 24, 1502– 1513. (Scopus citation: 1)
6 “A Concise Synthesis of (2R,3R)- and (2R,3S)-3-Hydroxypipecolic Acids, and Total Synthesis of (–)-Deoxoprosopinine and (+)-2-epi-Deoxoprosopinine from D- Glycals” Eur. J. Org. Chem. 2014, 25, 5557−5563. (Scopus citation: 5)
7 “Aza-Claisen rearrangement of 2-C-hydroxymethyl glycals as a versatile strategy towards synthesis of isofagomine and related biologically important azasugars” Org. Biomol. Chem. 2012, 10, 2760–2773. (Google Scholar citation: 28)
8 “AuIII-Halide/Phenylacetylene-Catalyzed Glycosylations Using 1-O-Acetylfuranoses and Pyranose 1,2-Orthoesters as Glycosyl Donors” Eur. J. Org.Chem. 2016, 3, 579–588. (Scopus citation: 7)