| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Synthesis of novel pyrrolidine 3,4-diol derivatives as inhibitors of alpha-L-fucosidases.
|
Org Biomol Chem
|
2009
|
0.85
|
|
2
|
Synthesis and anti-HIV activity of trivalent CD4-mimetic miniproteins.
|
Bioorg Med Chem
|
2007
|
0.80
|
|
3
|
Glycosidase inhibitors as potential HIV entry inhibitors?
|
Curr Drug Metab
|
2004
|
0.79
|
|
4
|
Three dimensional structure of a bacterial α-l-fucosidase with a 5-membered iminocyclitol inhibitor.
|
Bioorg Med Chem
|
2013
|
0.76
|
|
5
|
Allenyl sulfones and allenyl sulfides in the synthesis of 3-pyrrolines. A novel nucleophilic [3 + 2] cycloaddition on allenyl sulfones giving rearranged cycloadducts.
|
Org Lett
|
2009
|
0.75
|
|
6
|
Exploiting the ring strain in bicyclo[2.2.1]heptane systems for the stereoselective preparation of highly functionalized cyclopentene, dihydrofuran, pyrroline, and pyrrolidine scaffolds.
|
Org Lett
|
2011
|
0.75
|
|
7
|
Synthesis, biological evaluation, WAC and NMR studies of S-galactosides and non-carbohydrate ligands of cholera toxin based on polyhydroxyalkylfuroate moieties.
|
Chemistry
|
2013
|
0.75
|
|
8
|
Total asymmetric synthesis of monosaccharides and analogues.
|
Chimia (Aarau)
|
2011
|
0.75
|
|
9
|
Stereoselective synthesis of (2S,3S,4R,5S)-5-methylpyrrolidine-3,4-diol derivatives that are highly selective alpha-L-fucosidase inhibitors.
|
Chem Commun (Camb)
|
2005
|
0.75
|
|
10
|
Monosaccharides and analogues from simple achiral unsaturated compounds.
|
Chimia (Aarau)
|
2011
|
0.75
|
|
11
|
Synthesis and conformational analysis of novel trimeric maleimide cross-linking reagents.
|
J Org Chem
|
2007
|
0.75
|
|
12
|
Syntheses and biological activities of 1,4-iminoalditol derivatives as alpha-L-fucosidase inhibitors.
|
Chimia (Aarau)
|
2011
|
0.75
|
|
13
|
Rapid discovery of potent α-fucosidase inhibitors by in situ screening of a library of (pyrrolidin-2-yl)triazoles.
|
Org Biomol Chem
|
2014
|
0.75
|
|
14
|
Strain-promoted retro-Dieckmann-type condensation on [2.2.2]- and [2.2.1]bicyclic systems: a fragmentation reaction for the preparation of functionalized heterocycles and carbocycles.
|
Org Biomol Chem
|
2013
|
0.75
|
|
15
|
Synthesis and inhibitory activities of novel C-3 substituted azafagomines: a new type of selective inhibitors of α-L-fucosidases.
|
Bioorg Med Chem
|
2010
|
0.75
|