N-Spirofused Bicyclic Derivatives of 1-Deoxynojirimycin: Synthesis and Preliminary Biological Evaluation
Author:
Affiliation:
1. Department of Biotechnology and Bioscience; University of Milano Bicocca; Piazza Della Scienza 2 I 20126 Milan Italywww.unimib.it
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201600516/fullpdf
Reference34 articles.
1. 2007
2. A general strategy towards the synthesis of 1-N-iminosugar type glycosidase inhibitors: demonstration by the synthesis of d- as well as l-glucose type iminosugars (isofagomines)
3. Structure and synthesis of nojirimycin
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1. Systems With a Spirocyclic Heteroatom;Comprehensive Heterocyclic Chemistry IV;2022
2. Synthesis of Chiral 3,3ʹ-Disubstituted (S)-BINOL Derivatives via the Kumada and Suzuki Coupling and Their Antibacterial Activity;Russian Journal of General Chemistry;2020-08
3. Preparation of 1-deoxynojirimycin controlled release matrix pellets of capsules and evaluation in vitro-in vivo to enhance bioavailability;Journal of Drug Delivery Science and Technology;2019-08
4. Spiro Iminosugars: Structural Diversity and Synthetic Strategies;Topics in Heterocyclic Chemistry;2019
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