Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Facile C-N cleavage in a series of bridged lactams.
|
J Am Chem Soc
|
2005
|
1.37
|
2
|
Revisiting a classic approach to the Aspidosperma alkaloids: an intramolecular Schmidt reaction mediated synthesis of (+)-aspidospermidine.
|
J Org Chem
|
2005
|
1.31
|
3
|
Characterization of a Cdc42 protein inhibitor and its use as a molecular probe.
|
J Biol Chem
|
2013
|
1.24
|
4
|
Cation-pi control of regiochemistry of intramolecular schmidt reactions en route to bridged bicyclic lactams.
|
J Am Chem Soc
|
2007
|
1.18
|
5
|
Development of functionally selective, small molecule agonists at kappa opioid receptors.
|
J Biol Chem
|
2013
|
1.17
|
6
|
A combined intramolecular Diels-Alder/intramolecular schmidt reaction: formal synthesis of (+/-)-stenine.
|
Angew Chem Int Ed Engl
|
2002
|
1.14
|
7
|
Domino reactions that combine an azido-Schmidt ring expansion with the Diels-Alder reaction.
|
Org Lett
|
2004
|
1.14
|
8
|
Syntheses of the Stemona alkaloids (+/-)-stenine, (+/-)-neostenine, and (+/-)-13-epineostenine using a stereodivergent Diels-Alder/azido-Schmidt reaction.
|
J Am Chem Soc
|
2008
|
1.10
|
9
|
A tandem Prins/Schmidt reaction approach to marine alkaloids: formal and total syntheses of lepadiformines A and C.
|
Org Lett
|
2010
|
1.09
|
10
|
An expeditious total synthesis of (+/-)-stenine.
|
J Am Chem Soc
|
2005
|
1.08
|
11
|
Regioselective single and double conjugate additions to substituted cyclohexa-2,5-dienone monoacetals.
|
Org Lett
|
2005
|
1.07
|
12
|
Medium-bridged lactams: a new class of non-planar amides.
|
Org Biomol Chem
|
2010
|
1.05
|
13
|
Synthesis of N-alkyl-octahydroisoquinolin-1-one-8-carboxamide libraries using a tandem Diels-Alder/acylation sequence.
|
J Comb Chem
|
2007
|
1.05
|
14
|
Minor withanolides of Physalis longifolia: structure and cytotoxicity.
|
Chem Pharm Bull (Tokyo)
|
2012
|
1.04
|
15
|
Asymmetric total synthesis of dendrobatid alkaloid 251F.
|
J Am Chem Soc
|
2002
|
0.99
|
16
|
Overcoming product inhibition in catalysis of the intramolecular Schmidt reaction.
|
J Am Chem Soc
|
2013
|
0.97
|
17
|
Stability of medium-bridged twisted amides in aqueous solutions.
|
J Org Chem
|
2009
|
0.95
|
18
|
Asymmetric total synthesis of dendrobatid alkaloids: preparation of indolizidine 251F and its 3-desmethyl analogue using an intramolecular Schmidt reaction strategy.
|
J Am Chem Soc
|
2004
|
0.95
|
19
|
Chemotype-selective modes of action of κ-opioid receptor agonists.
|
J Biol Chem
|
2013
|
0.95
|
20
|
Synthesis and receptor profiling of Stemona alkaloid analogues reveal a potent class of sigma ligands.
|
Proc Natl Acad Sci U S A
|
2011
|
0.95
|
21
|
Identification of a small molecule yeast TORC1 inhibitor with a multiplex screen based on flow cytometry.
|
ACS Chem Biol
|
2012
|
0.95
|
22
|
Lewis acid-mediated reactions of alkyl azides with alpha,beta-unsaturated ketones.
|
Org Lett
|
2003
|
0.94
|
23
|
Explorations of stemona alkaloid-inspired analogues: skeletal modification and functional group diversification.
|
J Comb Chem
|
2008
|
0.94
|
24
|
First asymmetric total synthesis of (+)-sparteine.
|
Org Lett
|
2002
|
0.93
|
25
|
Efficient synthesis of gamma-lactams by a tandem reductive amination/lactamization sequence.
|
J Comb Chem
|
2008
|
0.93
|
26
|
1,3-allylic strain as a strategic diversification element for constructing libraries of substituted 2-arylpiperidines.
|
Angew Chem Int Ed Engl
|
2011
|
0.93
|
27
|
A competitive nucleotide binding inhibitor: in vitro characterization of Rab7 GTPase inhibition.
|
ACS Chem Biol
|
2012
|
0.92
|
28
|
Ring expansive routes to quinolizidine alkaloids: formal synthesis of (-)-lasubine II.
|
Org Lett
|
2003
|
0.92
|
29
|
Asymmetric Schmidt reaction of hydroxyalkyl azides with ketones.
|
J Am Chem Soc
|
2003
|
0.92
|
30
|
Identification and validation of novel small molecule disruptors of HuR-mRNA interaction.
|
ACS Chem Biol
|
2015
|
0.92
|
31
|
Optimization of potent hepatitis C virus NS3 helicase inhibitors isolated from the yellow dyes thioflavine S and primuline.
|
J Med Chem
|
2012
|
0.92
|
32
|
High-throughput screening identifies a bisphenol inhibitor of SV40 large T antigen ATPase activity.
|
J Biomol Screen
|
2011
|
0.91
|
33
|
Chemistry of bridged lactams and related heterocycles.
|
Chem Rev
|
2013
|
0.91
|
34
|
Unusual tethering effects in the Schmidt reaction of hydroxyalkyl azides with ketones: cation-pi and steric stabilization of a pseudoaxial phenyl group.
|
J Am Chem Soc
|
2003
|
0.90
|
35
|
Mechanism of the acid-promoted intramolecular schmidt reaction: theoretical assessment of the importance of lone pair-cation, cation-π, and steric effects in controlling regioselectivity.
|
J Org Chem
|
2011
|
0.90
|
36
|
Development of (E)-2-((1,4-dimethylpiperazin-2-ylidene)amino)-5-nitro-N-phenylbenzamide, ML336: Novel 2-amidinophenylbenzamides as potent inhibitors of venezuelan equine encephalitis virus.
|
J Med Chem
|
2014
|
0.89
|
37
|
Cation-n control of regiochemistry of intramolecular Schmidt reactions en route to bridged bicyclic lactams.
|
Org Lett
|
2009
|
0.89
|
38
|
Discovery of Small Molecule Kappa Opioid Receptor Agonist and Antagonist Chemotypes through a HTS and Hit Refinement Strategy.
|
ACS Chem Neurosci
|
2012
|
0.89
|
39
|
N-Alkyl-octahydroisoquinolin-1-one-8-carboxamides: a Novel Class of Selective, Nonbasic, Nitrogen-Containing κ-Opioid Receptor Ligands.
|
ACS Med Chem Lett
|
2010
|
0.88
|
40
|
Corey-Chaykovsky epoxidation of twisted amides: synthesis and reactivity of bridged spiro-epoxyamines.
|
J Am Chem Soc
|
2009
|
0.88
|
41
|
Nucleophilic addition to iminium ethers in the preparation of functionalized N-alkyl heterocycles.
|
J Org Chem
|
2007
|
0.88
|
42
|
Asymmetric total synthesis of alkaloids 223A and 6-epi-223A.
|
Org Lett
|
2009
|
0.87
|
43
|
Direct synthesis of medium-bridged twisted amides via a transannular cyclization strategy.
|
Org Lett
|
2009
|
0.87
|
44
|
Proximity effects in nucleophilic addition reactions to medium-bridged twisted lactams: remarkably stable tetrahedral intermediates.
|
J Am Chem Soc
|
2010
|
0.86
|
45
|
Intramolecular and Intermolecular Schmidt Reactions of Alkyl Azides with Aldehydes.
|
Tetrahedron
|
2007
|
0.86
|
46
|
(S)-N-(2,5-Dimethylphenyl)-1-(quinoline-8-ylsulfonyl)pyrrolidine-2-carboxamide as a small molecule inhibitor probe for the study of respiratory syncytial virus infection.
|
J Med Chem
|
2012
|
0.86
|
47
|
Reaction discovery using microfluidic-based multidimensional screening of polycyclic iminium ethers.
|
J Org Chem
|
2010
|
0.85
|
48
|
Three-component synthesis of 1,4-diazepin-5-ones and the construction of gamma-turn-like peptidomimetic libraries.
|
J Comb Chem
|
2008
|
0.84
|
49
|
Stereocontrol in a combined allylic azide rearrangement and intramolecular Schmidt reaction.
|
J Am Chem Soc
|
2012
|
0.84
|
50
|
Remote control of diastereoselectivity in intramolecular reactions of chiral allylsilanes.
|
J Am Chem Soc
|
2006
|
0.84
|
51
|
Synthesis and Cytotoxicity of Semisynthetic Withalongolide A Analogues.
|
ACS Med Chem Lett
|
2013
|
0.83
|
52
|
Modular synthesis of cyclic peptidomimetics inspired by gamma-turns.
|
Org Lett
|
2005
|
0.83
|
53
|
Small-molecule pyrimidine inhibitors of the cdc2-like (Clk) and dual specificity tyrosine phosphorylation-regulated (Dyrk) kinases: development of chemical probe ML315.
|
Bioorg Med Chem Lett
|
2013
|
0.82
|
54
|
Nonbonded, attractive cation-pi interactions in azide-mediated asymmetric ring expansion reactions.
|
J Org Chem
|
2008
|
0.82
|
55
|
A selective ATP-binding cassette subfamily G member 2 efflux inhibitor revealed via high-throughput flow cytometry.
|
J Biomol Screen
|
2012
|
0.82
|
56
|
Base-promoted reactions of bridged ketones and 1,3- and 1,4-haloalkyl azides: competitive alkylation vs azidation reactions of ketone enolates.
|
J Org Chem
|
2004
|
0.82
|
57
|
Parallel solid-phase synthesis of diaryltriazoles.
|
Beilstein J Org Chem
|
2012
|
0.81
|
58
|
Double conjugate addition of a nitropropionate ester to a quinone monoketal: synthesis of an advanced intermediate to (+/-)-gelsemine.
|
Org Lett
|
2007
|
0.81
|
59
|
Synthesis and reactivity of bicyclo[3.2.1]octanoid-derived cyclopropanes.
|
J Org Chem
|
2011
|
0.81
|
60
|
Synthesis and rearrangement of a bridged thioamide.
|
Chem Commun (Camb)
|
2009
|
0.81
|
61
|
One-pot synthesis of lactams using domino reactions: combination of Schmidt reaction with Sakurai and aldol reactions.
|
J Org Chem
|
2009
|
0.81
|
62
|
Synthesis of medium-bridged twisted lactams via cation-pi control of the regiochemistry of the intramolecular Schmidt reaction.
|
J Org Chem
|
2010
|
0.81
|
63
|
Structural characterization of N-protonated amides: regioselective N-activation of medium-bridged twisted lactams.
|
J Am Chem Soc
|
2010
|
0.80
|
64
|
The NIH's role in accelerating translational sciences.
|
Nat Biotechnol
|
2012
|
0.79
|
65
|
Synthesis of a small library of diketopiperazines as potential inhibitors of calpain.
|
Bioorg Med Chem Lett
|
2005
|
0.79
|
66
|
Optimization of potent and selective quinazolinediones: inhibitors of respiratory syncytial virus that block RNA-dependent RNA-polymerase complex activity.
|
J Med Chem
|
2014
|
0.79
|
67
|
Solution-phase parallel synthesis of a library of delta(2)-pyrazolines.
|
J Comb Chem
|
2007
|
0.79
|
68
|
Synthesis and conformational studies of dipeptides constrained by disubstituted 3-(aminoethoxy)propionic acid linkers.
|
J Org Chem
|
2004
|
0.78
|
69
|
Rearrangements of bicyclic nitrones to lactams: comparison of photochemical and modified Barton conditions.
|
J Org Chem
|
2003
|
0.78
|
70
|
An efficient computational model to predict protonation at the amide nitrogen and reactivity along the C-N rotational pathway.
|
Chem Commun (Camb)
|
2015
|
0.78
|
71
|
One-step synthesis of oxazoline and dihydrooxazine libraries.
|
J Comb Chem
|
2007
|
0.78
|
72
|
Stereodivergent synthesis of enantioenriched 4-hydroxy-2-cyclopentenones.
|
J Org Chem
|
2013
|
0.77
|
73
|
Ab initio approach to understanding the stereoselectivity of reactions between hydroxyalkyl azides and ketones.
|
J Org Chem
|
2004
|
0.77
|
74
|
In situ generation and intramolecular Schmidt reaction of keto azides in a microwave-assisted flow format.
|
Chemistry
|
2011
|
0.77
|
75
|
A concomitant allylic azide rearrangement/intramolecular azide-alkyne cycloaddition sequence.
|
Org Lett
|
2014
|
0.77
|
76
|
Benzylmorpholine analogs as selective inhibitors of lung cytochrome P450 2A13 for the chemoprevention of lung cancer in tobacco users.
|
Pharm Res
|
2013
|
0.77
|
77
|
Small-molecule libraries: naturally inspired oligomers.
|
Nat Chem
|
2012
|
0.77
|
78
|
Use of a tandem Prins/Friedel-Crafts reaction in the construction of the indeno-tetrahydropyridine core of the haouamine alkaloids: formal synthesis of (-)-haouamine A.
|
Org Lett
|
2011
|
0.77
|
79
|
High-Throughput Screening, Discovery, and Optimization To Develop a Benzofuran Class of Hepatitis C Virus Inhibitors.
|
ACS Comb Sci
|
2015
|
0.76
|
80
|
Synthesis, structural analysis, and reactivity of bridged orthoamides by intramolecular Schmidt reaction.
|
J Am Chem Soc
|
2010
|
0.76
|
81
|
Copper-catalyzed oxaziridine-mediated oxidation of C-H bonds.
|
J Org Chem
|
2012
|
0.76
|
82
|
Reactions of cyclopropanone acetals with alkyl azides: carbonyl addition versus ring-opening pathways.
|
J Org Chem
|
2007
|
0.75
|
83
|
One-pot, regiospecific assembly of (E)-benzamidines from δ- and γ-amino acids via an intramolecular aminoquinazolinone rearrangement.
|
Org Biomol Chem
|
2016
|
0.75
|
84
|
Highly stereoselective ring expansion reactions mediated by attractive cation-n interactions.
|
Angew Chem Int Ed Engl
|
2008
|
0.75
|
85
|
Automated three-component synthesis of a library of γ-lactams.
|
Beilstein J Org Chem
|
2012
|
0.75
|
86
|
Resolution of carboxylic acids using copper(I)-promoted removal of propargylic esters under neutral conditions.
|
J Org Chem
|
2011
|
0.75
|
87
|
The Development of an Aryloxazole Class of Hepatitis C Virus Inhibitors Targeting the Entry Stage of the Viral Replication Cycle.
|
J Med Chem
|
2017
|
0.75
|
88
|
Correction to "Structure-Activity Relationship Studies of Functionally Selective Kappa Opioid Receptor Agonists that Modulate ERK 1/2 Phosphorylation While Preserving G Protein Over βArrestin2 Signaling Bias".
|
ACS Chem Neurosci
|
2017
|
0.75
|
89
|
Synthesis of enantiomerically enriched (R)-5-tert-butylazepan-2-one using a hydroxyalkyl azide mediated ring-expansion reaction.
|
Nat Protoc
|
2008
|
0.75
|
90
|
Synthesis and structural study of cyclic 5-aminovaleric acid-linked beta-Ala-beta-Ala dipeptides.
|
Bioorg Med Chem Lett
|
2008
|
0.75
|
91
|
Stereoselectivity in nucleophilic additions to 3-azidoalkanals.
|
J Org Chem
|
2011
|
0.75
|