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- Asymmetric synthesis of 1-deoxyazasugars from chiral aziridines. Alok Singh, Bongchan Kim, Won Koo Lee, Hyun-Joon Ha
, Org. Biomol. Chem.
, 2011
, 9
, 1372
- Aza-Claisen rearrangement of 2-C-hydroxymethyl glycals as a versatile strategy towards synthesis of isofagomine and related biologically important azasugars. Y. Suman Reddy, Pavan K. Kancharla, Rashmi Roy, Yashwant D. Vankar
, Org. Biomol. Chem.
, 2012
, 10
, 2760
- Synthesis of iminosugar derivatives presenting naphthyl and alkyl amine interacting groups and binding to somatostatin receptors. Stephen Barron, Paul V. Murphy
, Med. Chem. Commun.
, 2014
, 5
, 1150
- Total syntheses of d-allo-1-deoxynojirimycin and l-talo-1-deoxynojirimycin via reductive cyclization. Subhash P. Chavan, Nilesh B. Dumare, Kailash P. Pawar
, RSC Adv.
, 2014
, 4
, 40852
- Introduction of C-alkyl branches to l-iminosugars changes their active site binding orientation. Atsushi Kato, Izumi Nakagome, Kosuke Yoshimura, Uta Kanekiyo, Mana Kishida, Kenta Shinzawa, Tian-Tian Lu, Yi-Xian Li, Robert J. Nash, George W. J. Fleet, Nobutada Tanaka, Chu-Yi Yu
, Org. Biomol. Chem.
, 2022
, 20
, 7250
- Synthesis of polyhydroxy piperidines and their analogues: a novel approach towards selective inhibitors of α-glucosidase. Ganesh Pandey, Kishor Chandra Bharadwaj, M. Islam Khan, K. S. Shashidhara, Vedavati G. Puranik
, Org. Biomol. Chem.
, 2008
, 6
, 2587
- Natural products from plants targeting key enzymes for the future development of antidiabetic agents. R. Mata, L. Flores-Bocanegra, B. Ovalle-Magallanes, M. Figueroa
, Nat. Prod. Rep.
, 2023
, 40
, 1198
- A new access to polyhydroxy piperidines of the azasugar class: synthesis and glycosidase inhibition studies. Ganesh Pandey, Manmohan Kapur, M. Islam Khan, Sushama M. Gaikwad
, Org. Biomol. Chem.
, 2003
, 1
, 3321
- Preparation of optically active 3-substituted piperidines via ring expansion: synthesis of 4-amino- and 4-fluoro-1,4,5-trideoxy-1,5-imino-D-ribitol and 1,5-dideoxy-1,5-imino-D-ribitol. Dae-Kee Kim, Ganghyeok Kim, Young-Woo Kim
, J. Chem. Soc., Perkin Trans. 1
, 1996
, 803