209 related articles for article (PubMed ID: 21426093)
1. Difluoromethylenated polyhydroxylated pyrrolidines: facile synthesis, crystal structure and biological evaluation.
Wang RW; Xu J; Lopez O; Bols M; Qing FL
Future Med Chem; 2009 Aug; 1(5):991-7. PubMed ID: 21426093
[TBL] [Abstract][Full Text] [Related]
2. Synthesis and biological evaluation of glycosidase inhibitors: gem-difluoromethylenated nojirimycin analogues.
Wang RW; Qiu XL; Bols M; Ortega-Caballero F; Qing FL
J Med Chem; 2006 May; 49(10):2989-97. PubMed ID: 16686540
[TBL] [Abstract][Full Text] [Related]
3. Asymmetric synthesis of 3-amino-4-hydroxy-2-(hydroxymethyl)pyrrolidines as potential glycosidase inhibitors.
Curtis KL; Evinson EL; Handa S; Singh K
Org Biomol Chem; 2007 Nov; 5(21):3544-53. PubMed ID: 17943217
[TBL] [Abstract][Full Text] [Related]
4. Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-4,4-difluoronojirimycin.
Wang RW; Qing FL
Org Lett; 2005 May; 7(11):2189-92. PubMed ID: 15901166
[TBL] [Abstract][Full Text] [Related]
5. Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines D and M.
Ribes C; Falomir E; Murga J; Carda M; Alberto Marco J
Org Biomol Chem; 2009 Apr; 7(7):1355-60. PubMed ID: 19300820
[TBL] [Abstract][Full Text] [Related]
6. Looking glass inhibitors: L-DMDP, a more potent and specific inhibitor of alpha-glucosidases than the enantiomeric natural product DMDP.
Yu CY; Asano N; Ikeda K; Wang MX; Butters TD; Wormald MR; Dwek RA; Winters AL; Nash RJ; Fleet GW
Chem Commun (Camb); 2004 Sep; (17):1936-7. PubMed ID: 15340609
[TBL] [Abstract][Full Text] [Related]
7. L-DMDP, L-homoDMDP and their C-3 fluorinated derivatives: synthesis and glycosidase-inhibition.
Li YX; Huang MH; Yamashita Y; Kato A; Jia YM; Wang WB; Fleet GW; Nash RJ; Yu CY
Org Biomol Chem; 2011 May; 9(9):3405-14. PubMed ID: 21423946
[TBL] [Abstract][Full Text] [Related]
8. γ-Aminoalcohol rearrangement applied to pentahydroxylated azepanes provides pyrrolidines epimeric to homoDMDP.
Jagadeesh Y; Tran AT; Luo B; Auberger N; Désiré J; Nakagawa S; Kato A; Zhang Y; Sollogoub M; Blériot Y
Org Biomol Chem; 2015 Mar; 13(11):3446-56. PubMed ID: 25666467
[TBL] [Abstract][Full Text] [Related]
9. Flexibility in the partial reduction of 2,5-disubstituted pyrroles: application to the synthesis of DMDP.
Donohoe TJ; Headley CE; Cousins RP; Cowley A
Org Lett; 2003 Apr; 5(7):999-1002. PubMed ID: 12659558
[TBL] [Abstract][Full Text] [Related]
10. Pyrrolidine-5,5-trans-lactams. 2. The use of X-ray crystal structure data in the optimization of P3 and P4 substituents.
Andrews DM; Chaignot H; Coomber BA; Good AC; Hind SL; Johnson MR; Jones PS; Mills G; Robinson JE; Skarzynski T; Slater MJ; Somers DO
Org Lett; 2002 Dec; 4(25):4479-82. PubMed ID: 12465917
[TBL] [Abstract][Full Text] [Related]
11. Isolation from Stevia rebaudiana of DMDP acetic acid, a novel iminosugar amino acid: synthesis and glycosidase inhibition profile of glycine and β-alanine pyrrolidine amino acids.
Martínez RF; Jenkinson SF; Nakagawa S; Kato A; Wormald MR; Fleet GWJ; Hollinshead J; Nash RJ
Amino Acids; 2019 Jul; 51(7):991-998. PubMed ID: 31079215
[TBL] [Abstract][Full Text] [Related]
12. Design, synthesis and preliminary evaluation of novel pyrrolidine derivatives as matrix metalloproteinase inhibitors.
Cheng XC; Wang Q; Fang H; Tang W; Xu WF
Eur J Med Chem; 2008 Oct; 43(10):2130-9. PubMed ID: 18362041
[TBL] [Abstract][Full Text] [Related]
13. Probing the aglycon binding site of a beta-glucosidase: a collection of C-1-modified 2,5-dideoxy-2,5-imino-D-mannitol derivatives and their structure-activity relationships as competitive inhibitors.
Wrodnigg TM; Diness F; Gruber C; Häusler H; Lundt I; Rupitz K; Steiner AJ; Stütz AE; Tarling CA; Withers SG; Wölfler H
Bioorg Med Chem; 2004 Jul; 12(13):3485-95. PubMed ID: 15186833
[TBL] [Abstract][Full Text] [Related]
14. Synthesis of isofagomine-pyrrolidine hybrid sugars and analogues of (-)-steviamine and (+)-hyacinthacine C5 using 1,3-dipolar cycloaddition reactions.
Lahiri R; Palanivel A; Kulkarni SA; Vankar YD
J Org Chem; 2014 Nov; 79(22):10786-800. PubMed ID: 25333970
[TBL] [Abstract][Full Text] [Related]
15. Synthesis and inhibitory activities of novel C-3 substituted azafagomines: a new type of selective inhibitors of α-L-fucosidases.
Moreno-Clavijo E; Carmona AT; Moreno-Vargas AJ; Rodríguez-Carvajal MA; Robina I
Bioorg Med Chem; 2010 Jul; 18(13):4648-60. PubMed ID: 20570156
[TBL] [Abstract][Full Text] [Related]
16. Five-membered iminocyclitol α-glucosidase inhibitors: synthetic, biological screening and in silico studies.
Guerreiro LR; Carreiro EP; Fernandes L; Cardote TA; Moreira R; Caldeira AT; Guedes RC; Burke AJ
Bioorg Med Chem; 2013 Apr; 21(7):1911-7. PubMed ID: 23419323
[TBL] [Abstract][Full Text] [Related]
17. α-Geminal disubstituted pyrrolidine iminosugars and their C-4-fluoro analogues: Synthesis, glycosidase inhibition and molecular docking studies.
Gavale KS; Chavan SR; Kumbhar N; Kawade S; Doshi P; Khan A; Dhavale DD
Bioorg Med Chem; 2017 Oct; 25(19):5148-5159. PubMed ID: 28751199
[TBL] [Abstract][Full Text] [Related]
18. Synthesis of all-cis 2,5-imino-2,5-dideoxy-fucitol and its evaluation as a potent fucosidase and galactosidase inhibitor.
Ak A; Prudent S; LeNouën D; Defoin A; Tarnus C
Bioorg Med Chem Lett; 2010 Dec; 20(24):7410-3. PubMed ID: 21050758
[TBL] [Abstract][Full Text] [Related]
19. Palladium-catalyzed DYKAT of butadiene monoepoxide: enantioselective total synthesis of (+)-DMDP, (-)-bulgecinine, and (+)-broussonetine G.
Trost BM; Horne DB; Woltering MJ
Chemistry; 2006 Aug; 12(25):6607-20. PubMed ID: 16807949
[TBL] [Abstract][Full Text] [Related]
20. Aziridine carboxylate from D-glucose: synthesis of polyhydroxylated piperidine, pyrrolidine alkaloids and study of their glycosidase inhibition.
Dhavale DD; Kumar KS; Chaudhari VD; Sharma T; Sabharwal SG; Prakashareddy J
Org Biomol Chem; 2005 Oct; 3(20):3720-6. PubMed ID: 16211108
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
