Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Novel 2-[(benzylamino)methyl]pyrrolidine-3,4-diol derivatives as alpha-mannosidase inhibitors and with antitumor activities against hematological and solid malignancies.
|
Bioorg Med Chem
|
2010
|
1.40
|
2
|
Rational design of indoleamine 2,3-dioxygenase inhibitors.
|
J Med Chem
|
2010
|
1.22
|
3
|
Organosulfur compounds: electrophilic reagents in transition-metal-catalyzed carbon-carbon bond-forming reactions.
|
Angew Chem Int Ed Engl
|
2005
|
0.99
|
4
|
Recent synthetic approaches toward non-anomeric spiroketals in natural products.
|
Molecules
|
2008
|
0.97
|
5
|
Silyl methallylsulfinates: efficient and powerful agents for the chemoselective silylation of alcohols, polyols, phenols and carboxylic acids.
|
Chem Commun (Camb)
|
2005
|
0.93
|
6
|
Structural insights into the specificity of Xyn10B from Paenibacillus barcinonensis and its improved stability by forced protein evolution.
|
J Biol Chem
|
2009
|
0.91
|
7
|
Synthesis of the C(1)-C(11) polyene fragment of apoptolidin with a new sulfur dioxide-based organic chemistry.
|
Chemistry
|
2005
|
0.90
|
8
|
Rational design of 4-aryl-1,2,3-triazoles for indoleamine 2,3-dioxygenase 1 inhibition.
|
J Med Chem
|
2012
|
0.85
|
9
|
Synthesis of novel pyrrolidine 3,4-diol derivatives as inhibitors of alpha-L-fucosidases.
|
Org Biomol Chem
|
2009
|
0.85
|
10
|
New efficient route to an advanced precursor of the AB spiroketal of spongistatins.
|
Org Lett
|
2007
|
0.85
|
11
|
Scope and limitations of the double [4+3]-cycloadditions of 2-oxyallyl cations to 2,2'-methylenedifuran and derivatives.
|
J Org Chem
|
2003
|
0.84
|
12
|
New synthetic seven-membered 1-azasugars displaying potent inhibition towards glycosidases and glucosylceramide transferase.
|
Chembiochem
|
2008
|
0.84
|
13
|
Short synthesis of the C16-C28 polyketide fragment of apoptolidin A aglycone.
|
Chem Commun (Camb)
|
2007
|
0.83
|
14
|
Total synthesis and determination of the absolute configuration of (-)-dolabriferol.
|
Angew Chem Int Ed Engl
|
2010
|
0.82
|
15
|
Palladium-catalyzed Stille cross-couplings of sulfonyl chlorides and organostannanes.
|
J Am Chem Soc
|
2003
|
0.82
|
16
|
New concise total synthesis of (+)-lentiginosine and some structural analogues.
|
J Org Chem
|
2005
|
0.81
|
17
|
Synthesis and conformational analysis of (alpha-D-galactosyl)phenylmethane and alpha-,beta-difluoromethane analogues: interactions with the plant lectin viscumin.
|
Chemistry
|
2009
|
0.81
|
18
|
Functionalized pyrrolidines inhibit alpha-mannosidase activity and growth of human glioblastoma and melanoma cells.
|
J Med Chem
|
2005
|
0.80
|
19
|
Tandem Staudinger-azaWittig mediated ring expansion: rapid access to new isofagomine-tetrahydroxyazepane hybrids.
|
Chem Commun (Camb)
|
2006
|
0.79
|
20
|
Glycosidase inhibitors as potential HIV entry inhibitors?
|
Curr Drug Metab
|
2004
|
0.79
|
21
|
Search for alpha-glucosidase inhibitors: new N-substituted valienamine and conduramine F-1 derivatives.
|
Bioorg Med Chem
|
2006
|
0.79
|
22
|
Palladium-catalyzed Suzuki-Miyaura cross-couplings of sulfonyl chlorides and boronic acids.
|
Org Lett
|
2004
|
0.79
|
23
|
The hetero-Diels-Alder addition of sulfur dioxide to 1-fluorobuta-1,3-dienes: the sofa conformations preferred by 6-fluorosultines (6-fluoro-3,6-dihydro-1,2-oxathiin-2-oxides) enjoy enthalpic and conformational Anomeric effects.
|
Chemistry
|
2002
|
0.79
|
24
|
Iron-catalyzed desulfinylative C-C cross-coupling reactions of sulfonyl chlorides with grignard reagents.
|
Angew Chem Int Ed Engl
|
2008
|
0.79
|
25
|
A C-linked disaccharide analogue of Thomsen-Friedenreich epitope induces a strong immune response in mice.
|
Chemistry
|
2012
|
0.78
|
26
|
Nucleophilic opening of epoxyazepanes: expanding the family of polyhydroxyazepane-based glycosidase inhibitors.
|
Org Biomol Chem
|
2006
|
0.78
|
27
|
Design and synthesis of acetamido tri- and tetra-hydroxyazepanes: potent and selective beta-N-acetylhexosaminidase inhibitors.
|
Bioorg Med Chem
|
2009
|
0.78
|
28
|
Total asymmetric synthesis of (-)-conduramine B-1 and of its enantiomer. N-Benzyl derivatives of conduramine B-1 are beta-glucosidase inhibitors.
|
Bioorg Med Chem Lett
|
2005
|
0.78
|
29
|
An efficient combinatorial method for the discovery of glycosidase inhibitors.
|
Chembiochem
|
2002
|
0.78
|
30
|
Chemoselective C-H bond activation: ligand and solvent free iron-catalyzed oxidative C-C cross-coupling of tertiary amines with terminal alkynes. Reaction scope and mechanism.
|
Org Lett
|
2009
|
0.78
|
31
|
Stereoselective syntheses of 1,4-dideoxy-1,4-imino-octitols and novel tetrahydroxyindolizidines.
|
J Org Chem
|
2003
|
0.78
|
32
|
Synthesis of optically active 5-alkoxy-6-methylcyclohex-2-en-1-ones and 4-alkoxy-5-methylcyclopent-1-enyl benzoate.
|
J Org Chem
|
2009
|
0.77
|
33
|
Ab initio and experimental studies on the hetero-Diels-Alder and cheletropic additions of sulfur dioxide to (E)-1-methoxybutadiene: a mechanism involving three molecules of SO(2).
|
J Org Chem
|
2002
|
0.77
|
34
|
Synthesis of new oxathiazinane dioxides and their in vitro cancer cell growth inhibitory activity.
|
Bioorg Med Chem Lett
|
2009
|
0.77
|
35
|
Desulfinylation of prop-2-enesulfinic acid: experimental results and mechanistic theoretical analysis.
|
J Am Chem Soc
|
2009
|
0.77
|
36
|
The first synthesis of substituted azepanes mimicking monosaccharides: a new class of potent glycosidase inhibitors.
|
Org Biomol Chem
|
2004
|
0.77
|
37
|
Sulfur dioxide mediated one-pot, three- and four-component syntheses of polyfunctional sulfonamides and sulfonic esters: study of the stereoselectivity of the ene reaction of sulfur dioxide.
|
J Org Chem
|
2004
|
0.77
|
38
|
Synthesis of (E,Z)-1-alkoxy-3-acyloxy-2-methylpenta-1,3-dienes via Danishefsky-type dienes or O-acylation of enones.
|
J Org Chem
|
2009
|
0.77
|
39
|
Concise synthesis of complicated polypropionates through one-pot dissymmetrical two-directional chain elongation.
|
Chemistry
|
2011
|
0.76
|
40
|
The anti-lymphoma activity of APO866, an inhibitor of nicotinamide adenine dinucleotide biosynthesis, is potentialized when used in combination with anti-CD20 antibody.
|
Leuk Lymphoma
|
2014
|
0.76
|
41
|
Anti-cancer activity of 5-O-alkyl 1,4-imino-1,4-dideoxyribitols.
|
Bioorg Med Chem
|
2011
|
0.76
|
42
|
Polysulfones: catalysts for alkene isomerization.
|
Angew Chem Int Ed Engl
|
2004
|
0.76
|
43
|
Palladium-catalyzed desulfitative Mizoroki-Heck couplings of sulfonyl chlorides with mono- and disubstituted olefins: rhodium-catalyzed desulfitative heck-type reactions under phosphine- and base-free conditions.
|
Chemistry
|
2005
|
0.76
|
44
|
Total asymmetric syntheses of β-hydroxy-δ-lactones via Umpolung with sulfur dioxide.
|
J Org Chem
|
2011
|
0.75
|
45
|
Expeditious asymmetric synthesis of a stereoheptad corresponding to the C(19)-C(27)-ansa chain of rifamycins: formal total synthesis of Rifamycin S.
|
Chemistry
|
2005
|
0.75
|
46
|
Polysulfones: solid organic catalysts for the chemoselective cleavage of methyl-substituted allyl ethers under neutral conditions.
|
Chem Commun (Camb)
|
2004
|
0.75
|
47
|
Synthesis of branched seven-membered 1-N-iminosugars and their evaluation as glycosidase inhibitors.
|
Carbohydr Res
|
2011
|
0.75
|
48
|
Spirocyclopropyl pyrrolidines as a new series of alpha-L-fucosidase inhibitors.
|
Bioorg Med Chem
|
2006
|
0.75
|
49
|
Synthesis of enantiomerically pure 1,2-diamine derivatives of 7-azabicyclo[2.2.1]heptane. New leads as glycosidase inhibitors and rigid scaffolds for the preparation of peptide analogues.
|
J Org Chem
|
2003
|
0.75
|
50
|
The hetero-Diels-Alder addition of sulfur dioxide: the pseudo-chair conformation of a 4,5-dialkylsultine.
|
Chemistry
|
2003
|
0.75
|
51
|
Mechanism of the diphenyldisulfone-catalyzed isomerization of alkenes. Origin of the chemoselectivity: experimental and quantum chemistry studies.
|
J Am Chem Soc
|
2006
|
0.75
|
52
|
The spirocyclopropyl moiety as a methyl surrogate in the structure of l-fucosidase and l-rhamnosidase inhibitors.
|
Bioorg Med Chem
|
2009
|
0.75
|
53
|
The use of levoglucosenone and isolevoglucosenone as templates for the construction of C-linked disaccharides.
|
Carbohydr Res
|
2006
|
0.75
|
54
|
The catalyzed desulfinylative allylation of carbonyl compounds with alk-2-enesulfonyl chlorides and silyl alk-2-enesulfinates.
|
Chemistry
|
2010
|
0.75
|
55
|
Glycochemistry today.
|
Chimia (Aarau)
|
2011
|
0.75
|
56
|
BCl3-mediated ene reaction of sulfur dioxide and unfunctionalized alkenes.
|
Chemistry
|
2010
|
0.75
|
57
|
A short and convenient synthesis of 1-deoxymannojirimycin and N-oxy analogues from D-fructose.
|
J Org Chem
|
2009
|
0.75
|
58
|
Allyl, methallyl, prenyl, and methylprenyl ethers as protected alcohols: their selective cleavage with diphenyldisulfone under neutral conditions.
|
Org Lett
|
2004
|
0.75
|
59
|
Amide formation in one pot from carboxylic acids and amines via carboxyl and sulfinyl mixed anhydrides.
|
Org Lett
|
2013
|
0.75
|
60
|
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
|
61
|
The norbornene mystery revealed.
|
Chem Commun (Camb)
|
2010
|
0.75
|
62
|
Synthesis of long-chain polyketide fragments by reaction of 1,3-dioxy-1,3-dienes with allylsilanes: umpolung with sulfur dioxide.
|
Org Lett
|
2004
|
0.75
|
63
|
Synthesis of d- and l-2,3-trans-3,4-cis-4,5-trans-3,4-dihydroxy-5-hydroxymethylproline and tripeptides containing them.
|
J Org Chem
|
2004
|
0.75
|
64
|
Synthesis and glycosidase inhibitory activities of 2-(aminoalkyl)pyrrolidine-3,4-diol derivatives.
|
Bioorg Med Chem
|
2003
|
0.75
|
65
|
First asymmetric synthesis of the cyclohexanone subunit of baconipyrones A and B. Revision of its structure.
|
Org Lett
|
2004
|
0.75
|
66
|
Palladium-catalyzed conversion of beta,gamma-unsaturated silyl sulfinates into (E)-alkenes: asymmetric synthesis of polypropionate fragments.
|
J Org Chem
|
2004
|
0.75
|
67
|
Carbohydrates in sustainable development, Part 1. Renewable resources for chemistry and biotechnology. Preface.
|
Top Curr Chem
|
2010
|
0.75
|
68
|
C-linked disaccharide analogue of the Thomsen-Friedenreich (T)-epitope alpha-O-conjugated to L-serine.
|
Chemistry
|
2005
|
0.75
|
69
|
Short diastereoselective synthesis of the C1-C13 (AB spiroacetal) and C17-C28 fragments (CD spiroacetal) of spongistatin 1 and 2 through double chain-elongation reactions.
|
Chemistry
|
2010
|
0.75
|
70
|
Synthesis and glycosidase inhibitory activity of 1-amino-3,6-anhydro-1-deoxy-D-sorbitol derivatives.
|
Bioorg Chem
|
2009
|
0.75
|
71
|
Synthesis of [(2S,3S,4R)-3,4-dihydroxypyrrolidin-2-yl]-5-methylfuran-4-carboxylic acid derivatives: new leads as selective beta-galactosidase inhibitors.
|
Bioorg Med Chem Lett
|
2002
|
0.75
|
72
|
Equilibrium and kinetic deuterium isotope effects on the hetero-Diels-Alder addition of sulfur dioxide.
|
Angew Chem Int Ed Engl
|
2003
|
0.75
|
73
|
Sulfur dioxide-mediated syntheses of polyfunctional alkenes and (E,Z)- and (E,E)-2,4-dien-1-ones.
|
Org Lett
|
2005
|
0.75
|
74
|
Amides in one pot from carboxylic acids and amines via sulfinylamides.
|
Org Lett
|
2014
|
0.75
|