Rank |
Title |
Year |
PubWeight™‹?› |
1
|
Isomerization/Recyclization of some 5-Ethoxycarbonyl-pyrimidines.
|
2005
|
0.90
|
2
|
A New and Efficient Approach to the Synthesis of Nicotine and Anabasine Analogues.
|
2009
|
0.88
|
3
|
Synthesis of Novel Functionalized 4-Aza-2,3-Didehydropodophyllotoxin Derivatives with Potential Antitumor Activity.
|
2010
|
0.82
|
4
|
Dithiolopyranthione Synthesis, Spectroscopy and an Unusual Reactivity with DDQ.
|
2013
|
0.81
|
5
|
Synthesis of 1-(Substituted Phenylcarbonyl/sulfonylamino)-1,2,3,6-tetrahydropyridine-5-carboxylic acid diethylamides as Potential Anti-inflammatory Agents.
|
2006
|
0.78
|
6
|
Synthesis of Substituted N-[4(5-Methyl/phenyl-1,3,4-oxadiazol-2-yl)-3,6-dihydropyridin-1(2H)-yl]benzamide/benzene Sulfonamides as Anti-Inflammatory and Anti-Cancer Agents.
|
2009
|
0.77
|
7
|
Synthesis and Cytotoxic Evaluation of Pyrrole Hetarylazoles Containing Benzimidazole/Pyrazolone/1,3,4-Oxadiazole Motifs.
|
2015
|
0.75
|
8
|
Bichalcophenes: A Concise Synthesis of Formyl Ester- and Cyano Ester-Substituted Bithiophenes, Bifurans, and Furanothiophenes.
|
2010
|
0.75
|
9
|
Synthesis and chemical reactivity of a 6-Me-3,2-hydroxypyridinone dithiazolide with primary amines: a route to new hexadentate chelators for hard metal(III) ions.
|
2015
|
0.75
|
10
|
Application of Suzuki-Miyaura and Buchwald-Hartwig Cross-coupling Reactions to the Preparation of Substituted 1,2,4-Benzotriazine 1-Oxides Related to the Antitumor Agent Tirapazamine.
|
2015
|
0.75
|
11
|
The Thermal Instability of 2,4 and 2,6-N-Alkylamino Disubstituted and 2-N-Alkylamino Substituted Nitrobenzenes in Weakly Alkaline Solution: sec-Amino Effect.
|
2015
|
0.75
|
12
|
Synthesis and Investigation of Mixed μ-Opioid and δ-Opioid Agonists as Possible Bivalent Ligands for Treatment of Pain.
|
2016
|
0.75
|
13
|
Synthesis of 2-(N-Benzylpyrrolyl)-benzimidazoles Using Polyphosphoric Acid Prompted Cyclocondensation.
|
2010
|
0.75
|
14
|
Substituted 2,4,6-triamino-1,3,5-thiadiazinium salts: a new heteroaromatic system.
|
1971
|
0.75
|