| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
Palladium-catalyzed coupling reactions of aryl chlorides.
|
Angew Chem Int Ed Engl
|
2002
|
3.51
|
|
2
|
Enantioselective alkyl-alkyl Suzuki cross-couplings of unactivated homobenzylic halides.
|
J Am Chem Soc
|
2008
|
2.35
|
|
3
|
Catalytic asymmetric Hiyama cross-couplings of racemic alpha-bromo esters.
|
J Am Chem Soc
|
2008
|
2.33
|
|
4
|
Asymmetric nickel-catalyzed Negishi cross-couplings of secondary alpha-bromo amides with organozinc reagents.
|
J Am Chem Soc
|
2005
|
2.27
|
|
5
|
Suzuki cross-couplings of unactivated secondary alkyl bromides and iodides.
|
J Am Chem Soc
|
2004
|
2.09
|
|
6
|
Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides.
|
J Am Chem Soc
|
2005
|
2.06
|
|
7
|
Nickel-catalyzed asymmetric negishi cross-couplings of secondary allylic chlorides with alkylzincs.
|
J Am Chem Soc
|
2008
|
2.03
|
|
8
|
Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides.
|
J Am Chem Soc
|
2002
|
1.96
|
|
9
|
Catalytic asymmetric synthesis of piperidine derivatives through the [4 + 2] annulation of imines with allenes.
|
J Am Chem Soc
|
2005
|
1.94
|
|
10
|
Amino alcohols as ligands for nickel-catalyzed suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids.
|
J Am Chem Soc
|
2006
|
1.87
|
|
11
|
Synthesis of functionalized cyclopentenes through catalytic asymmetric [3+2] cycloadditions of allenes with enones.
|
Angew Chem Int Ed Engl
|
2006
|
1.76
|
|
12
|
Phosphine-catalyzed enantioselective synthesis of oxygen heterocycles.
|
Angew Chem Int Ed Engl
|
2009
|
1.67
|
|
13
|
Nickel-catalyzed asymmetric cross-couplings of racemic propargylic halides with arylzinc reagents.
|
J Am Chem Soc
|
2008
|
1.65
|
|
14
|
Asymmetric carbon-carbon bond formation gamma to a carbonyl group: phosphine-catalyzed addition of nitromethane to allenes.
|
J Am Chem Soc
|
2009
|
1.59
|
|
15
|
Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides.
|
J Am Chem Soc
|
2003
|
1.58
|
|
16
|
Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins.
|
J Am Chem Soc
|
2010
|
1.58
|
|
17
|
Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings.
|
J Am Chem Soc
|
2011
|
1.52
|
|
18
|
Academic cross-fertilization by public screening yields a remarkable class of protein phosphatase methylesterase-1 inhibitors.
|
Proc Natl Acad Sci U S A
|
2011
|
1.52
|
|
19
|
Nickel/bis(oxazoline)-catalyzed asymmetric Kumada reactions of alkyl electrophiles: cross-couplings of racemic alpha-bromoketones.
|
J Am Chem Soc
|
2010
|
1.52
|
|
20
|
Suzuki cross-couplings of alkyl tosylates that possess beta hydrogen atoms: synthetic and mechanistic studies.
|
Angew Chem Int Ed Engl
|
2002
|
1.51
|
|
21
|
Catalytic asymmetric cross-couplings of racemic alpha-bromoketones with arylzinc reagents.
|
Angew Chem Int Ed Engl
|
2009
|
1.47
|
|
22
|
Asymmetric Suzuki cross-couplings of activated secondary alkyl electrophiles: arylations of racemic alpha-chloroamides.
|
J Am Chem Soc
|
2010
|
1.46
|
|
23
|
Toward an improved understanding of the unusual reactivity of Pd0/trialkylphosphane catalysts in cross-couplings of alkyl electrophiles: quantifying the factors that determine the rate of oxidative addition.
|
Angew Chem Int Ed Engl
|
2003
|
1.40
|
|
24
|
A versatile method for Suzuki cross-coupling reactions of nitrogen heterocycles.
|
Angew Chem Int Ed Engl
|
2006
|
1.39
|
|
25
|
Stille cross-couplings of unactivated secondary alkyl halides using monoorganotin reagents.
|
J Am Chem Soc
|
2005
|
1.38
|
|
26
|
Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides.
|
J Am Chem Soc
|
2011
|
1.36
|
|
27
|
New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles.
|
J Am Chem Soc
|
2012
|
1.34
|
|
28
|
Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates.
|
J Am Chem Soc
|
2003
|
1.32
|
|
29
|
Enantioselective Staudinger synthesis of beta-lactams catalyzed by a planar-chiral nucleophile.
|
J Am Chem Soc
|
2002
|
1.30
|
|
30
|
Alkyl-alkyl suzuki cross-couplings of unactivated secondary alkyl halides at room temperature.
|
J Am Chem Soc
|
2007
|
1.29
|
|
31
|
Elucidating reactivity differences in palladium-catalyzed coupling processes: the chemistry of palladium hydrides.
|
J Am Chem Soc
|
2004
|
1.24
|
|
32
|
Boronic acids: new coupling partners in room-temperature Suzuki reactions of alkyl bromides. Crystallographic characterization of an oxidative-addition adduct generated under remarkably mild conditions.
|
J Am Chem Soc
|
2002
|
1.24
|
|
33
|
Umpolung of Michael acceptors catalyzed by N-heterocyclic carbenes.
|
J Am Chem Soc
|
2006
|
1.23
|
|
34
|
Intramolecular Heck reactions of unactivated alkyl halides.
|
J Am Chem Soc
|
2007
|
1.23
|
|
35
|
Nickel-catalyzed Negishi arylations of propargylic bromides: a mechanistic investigation.
|
J Am Chem Soc
|
2014
|
1.22
|
|
36
|
Phosphine-catalyzed formation of carbon-sulfur bonds: catalytic asymmetric synthesis of gamma-thioesters.
|
J Am Chem Soc
|
2010
|
1.22
|
|
37
|
Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations.
|
J Am Chem Soc
|
2013
|
1.21
|
|
38
|
Cu(I)/bis(azaferrocene)-catalyzed enantioselective synthesis of beta-lactams via couplings of alkynes with nitrones.
|
J Am Chem Soc
|
2002
|
1.18
|
|
39
|
Enantioconvergent cross-couplings of racemic alkylmetal reagents with unactivated secondary alkyl electrophiles: catalytic asymmetric Negishi α-alkylations of N-Boc-pyrrolidine.
|
J Am Chem Soc
|
2013
|
1.17
|
|
40
|
Catalytic enantioselective synthesis of oxindoles and benzofuranones that bear a quaternary stereocenter.
|
Angew Chem Int Ed Engl
|
2003
|
1.17
|
|
41
|
Phosphine-catalyzed asymmetric additions of malonate esters to {gamma}-substituted allenoates and allenamides.
|
Proc Natl Acad Sci U S A
|
2010
|
1.17
|
|
42
|
Nickel-catalyzed coupling reactions of alkyl electrophiles, including unactivated tertiary halides, to generate carbon-boron bonds.
|
J Am Chem Soc
|
2012
|
1.17
|
|
43
|
Enantioselective alkenylation via nickel-catalyzed cross-coupling with organozirconium reagents.
|
J Am Chem Soc
|
2010
|
1.16
|
|
44
|
A new copper-catalyzed [3 + 2] cycloaddition: enantioselective coupling of terminal alkynes with azomethine imines to generate five-membered nitrogen heterocycles.
|
J Am Chem Soc
|
2003
|
1.15
|
|
45
|
Application of a new chiral phosphepine to the catalytic asymmetric synthesis of highly functionalized cyclopentenes that bear an array of heteroatom-substituted quaternary stereocenters.
|
J Am Chem Soc
|
2011
|
1.14
|
|
46
|
Catalytic asymmetric Staudinger reactions to form beta-lactams: an unanticipated dependence of diastereoselectivity on the choice of the nitrogen substituent.
|
J Am Chem Soc
|
2005
|
1.13
|
|
47
|
Hiyama reactions of activated and unactivated secondary alkyl halides catalyzed by a nickel/norephedrine complex.
|
Angew Chem Int Ed Engl
|
2007
|
1.13
|
|
48
|
Alkyl-alkyl Suzuki cross-coupling of unactivated secondary alkyl chlorides.
|
Angew Chem Int Ed Engl
|
2010
|
1.12
|
|
49
|
Kinetic resolutions of azomethine imines via copper-catalyzed [3 + 2] cycloadditions.
|
J Am Chem Soc
|
2005
|
1.10
|
|
50
|
Copper-catalyzed asymmetric N-H insertion reactions: couplings of diazo compounds with carbamates to generate alpha-amino acids.
|
J Am Chem Soc
|
2007
|
1.10
|
|
51
|
Nickel/bis(oxazoline)-catalyzed asymmetric Negishi arylations of racemic secondary benzylic electrophiles to generate enantioenriched 1,1-diarylalkanes.
|
J Am Chem Soc
|
2013
|
1.09
|
|
52
|
Transition-metal-catalyzed alkylations of amines with alkyl halides: photoinduced, copper-catalyzed couplings of carbazoles.
|
Angew Chem Int Ed Engl
|
2013
|
1.08
|
|
53
|
Nickel-catalyzed enantioselective cross-couplings of racemic secondary electrophiles that bear an oxygen leaving group.
|
J Am Chem Soc
|
2012
|
1.08
|
|
54
|
Photoinduced Ullmann C-N coupling: demonstrating the viability of a radical pathway.
|
Science
|
2012
|
1.07
|
|
55
|
Method for palladium-catalyzed cross-couplings of simple alkyl chlorides: Suzuki reactions catalyzed by [Pd2(dba)3]/PCy3.
|
Angew Chem Int Ed Engl
|
2002
|
1.07
|
|
56
|
Catalytic enantioselective cross-couplings of secondary alkyl electrophiles with secondary alkylmetal nucleophiles: Negishi reactions of racemic benzylic bromides with achiral alkylzinc reagents.
|
J Am Chem Soc
|
2012
|
1.06
|
|
57
|
Catalytic enantioselective O-H insertion reactions.
|
J Am Chem Soc
|
2006
|
1.05
|
|
58
|
Asymmetric synthesis of highly substituted beta-lactones by nucleophile-catalyzed [2+2] cycloadditions of disubstituted ketenes with aldehydes.
|
Angew Chem Int Ed Engl
|
2004
|
1.05
|
|
59
|
Nickel-catalyzed cross-couplings of organosilicon reagents with unactivated secondary alkyl bromides.
|
J Am Chem Soc
|
2004
|
1.05
|
|
60
|
Kinetic resolutions of indolines by a nonenzymatic acylation catalyst.
|
J Am Chem Soc
|
2006
|
1.04
|
|
61
|
A straightforward and mild synthesis of functionalized 3-alkynoates.
|
Angew Chem Int Ed Engl
|
2004
|
1.04
|
|
62
|
Catalytic enantioselective synthesis of quaternary stereocenters via intermolecular C-acylation of silyl ketene acetals: dual activation of the electrophile and the nucleophile.
|
J Am Chem Soc
|
2003
|
1.03
|
|
63
|
Photoinduced, copper-catalyzed alkylation of amides with unactivated secondary alkyl halides at room temperature.
|
J Am Chem Soc
|
2014
|
1.02
|
|
64
|
A new family of nucleophiles for photoinduced, copper-catalyzed cross-couplings via single-electron transfer: reactions of thiols with aryl halides under mild conditions (O °C).
|
J Am Chem Soc
|
2013
|
1.01
|
|
65
|
Catalytic asymmetric synthesis of secondary nitriles via stereoconvergent Negishi arylations and alkenylations of racemic α-bromonitriles.
|
J Am Chem Soc
|
2012
|
1.00
|
|
66
|
A mild, palladium-catalyzed method for the dehydrohalogenation of alkyl bromides: synthetic and mechanistic studies.
|
J Am Chem Soc
|
2012
|
1.00
|
|
67
|
A versatile approach to Ullmann C-N couplings at room temperature: new families of nucleophiles and electrophiles for photoinduced, copper-catalyzed processes.
|
J Am Chem Soc
|
2013
|
0.99
|
|
68
|
Parallel kinetic resolution of 4-alkynals catalyzed by Rh(I)/Tol-BINAP: synthesis of enantioenriched cyclobutanones and cyclopentenones.
|
J Am Chem Soc
|
2003
|
0.99
|
|
69
|
Catalytic asymmetric C-N bond formation: phosphine-catalyzed intra- and intermolecular γ-addition of nitrogen nucleophiles to allenoates and alkynoates.
|
Angew Chem Int Ed Engl
|
2013
|
0.98
|
|
70
|
Catalytic asymmetric synthesis of tertiary alkyl chlorides.
|
Angew Chem Int Ed Engl
|
2007
|
0.98
|
|
71
|
Room-temperature Stille cross-couplings of alkenyltin reagents and functionalized alkyl bromides that possess beta hydrogens.
|
J Am Chem Soc
|
2003
|
0.95
|
|
72
|
The first applications of carbene ligands in cross-couplings of alkyl electrophiles: sonogashira reactions of unactivated alkyl bromides and iodides.
|
J Am Chem Soc
|
2003
|
0.94
|
|
73
|
Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds.
|
Angew Chem Int Ed Engl
|
2008
|
0.94
|
|
74
|
Catalytic asymmetric couplings of ketenes with aldehydes to generate enol esters.
|
Angew Chem Int Ed Engl
|
2005
|
0.94
|
|
75
|
Enantioselective Carbon-Sulfur Bond Formation: γ Additions of Aryl Thiols to Allenoates Catalyzed by a Chiral Phosphepine.
|
Chem Sci
|
2011
|
0.93
|
|
76
|
Nucleophile-catalyzed asymmetric acylations of silyl ketene imines: application to the enantioselective synthesis of verapamil.
|
Angew Chem Int Ed Engl
|
2005
|
0.93
|
|
77
|
Enantioselective synthesis of protected amines by the catalytic asymmetric addition of hydrazoic acid to ketenes.
|
Angew Chem Int Ed Engl
|
2007
|
0.90
|
|
78
|
Application of a new family of P,N ligands to the highly enantioselective hydrosilylation of aryl alkyl and dialkyl ketones.
|
Angew Chem Int Ed Engl
|
2002
|
0.90
|
|
79
|
Catalytic asymmetric synthesis of tertiary alkyl fluorides: Negishi cross-couplings of racemic α,α-dihaloketones.
|
J Am Chem Soc
|
2014
|
0.90
|
|
80
|
Nickel-catalyzed Negishi cross-couplings of secondary nucleophiles with secondary propargylic electrophiles at room temperature.
|
Angew Chem Int Ed Engl
|
2008
|
0.89
|
|
81
|
Stereoconvergent arylations and alkenylations of unactivated alkyl electrophiles: catalytic enantioselective synthesis of secondary sulfonamides and sulfones.
|
J Am Chem Soc
|
2014
|
0.89
|
|
82
|
Asymmetric [3 + 2] annulations catalyzed by a planar-chiral derivative of DMAP.
|
Chem Commun (Camb)
|
2006
|
0.88
|
|
83
|
Pd/P(t-Bu)(3)-Catalyzed Suzuki Cross-Couplings in the Presence of Water.
|
Adv Synth Catal
|
2010
|
0.87
|
|
84
|
A novel rhodium-catalyzed reduction-oxidation process: reaction of 4-alkynals with phenol to provide cis-4-alkenoates.
|
Angew Chem Int Ed Engl
|
2002
|
0.87
|
|
85
|
Biphenyl-derived phosphepines as chiral nucleophilic catalysts: enantioselective [4+1] annulations to form functionalized cyclopentenes.
|
Angew Chem Int Ed Engl
|
2014
|
0.86
|
|
86
|
Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition.
|
J Am Chem Soc
|
2012
|
0.86
|
|
87
|
Cross-couplings of alkyl electrophiles under "ligandless" conditions: Negishi reactions of organozirconium reagents.
|
J Am Chem Soc
|
2004
|
0.86
|
|
88
|
Catalytic enantioselective construction of all-carbon quaternary stereocenters: synthetic and mechanistic studies of the C-acylation of silyl ketene acetals.
|
J Am Chem Soc
|
2005
|
0.86
|
|
89
|
PALLADIUM-CATALYZED ALKYL-ALKYL SUZUKI CROSS-COUPLINGS OF PRIMARY ALKYL BROMIDES AT ROOM-TEMPERATURE: (13-CHLOROTRIDECYLOXY)TRIETHYLSILANE [Silane, [(13-chlorotridecyl)oxy]triethyl-].
|
Organic Synth
|
2010
|
0.85
|
|
90
|
A unique rhodium-catalyzed rearrangement process: isomerization of an alkyne to a 1,3-diene with concomitant migration of a formyl group. An expeditious route to dienals from readily available 4-alkynals.
|
Chem Commun (Camb)
|
2002
|
0.84
|
|
91
|
Catalytic asymmetric synthesis of esters from ketenes.
|
J Am Chem Soc
|
2005
|
0.84
|
|
92
|
Enantioselective synthesis of cyclopentenones via rhodium-catalyzed kinetic resolution and desymmetrization of 4-alkynals.
|
J Am Chem Soc
|
2002
|
0.83
|
|
93
|
Enantioselective nucleophile-catalyzed synthesis of tertiary alkyl fluorides via the α-fluorination of ketenes: synthetic and mechanistic studies.
|
J Am Chem Soc
|
2014
|
0.82
|
|
94
|
Enantioselective addition of amines to ketenes catalyzed by a planar-chiral derivative of PPY: possible intervention of chiral Brønsted-acid catalysis.
|
J Am Chem Soc
|
2002
|
0.82
|
|
95
|
Nonenzymatic dynamic kinetic resolution of secondary alcohols via enantioselective acylation: synthetic and mechanistic studies.
|
J Am Chem Soc
|
2012
|
0.82
|
|
96
|
NICKEL-CATALYZED ENANTIOSELECTIVE NEGISHI CROSS-COUPLINGS OF RACEMIC SECONDARY α-BROMO AMIDES WITH ALKYLZINC REAGENTS: (S)-N-BENZYL-7-CYANO-2-ETHYL-N-PHENYLHEPTANAMIDE.
|
Organic Synth
|
2010
|
0.81
|
|
97
|
Catalytic enantioselective cyclization/cross-coupling with alkyl electrophiles.
|
J Am Chem Soc
|
2014
|
0.80
|
|
98
|
Room-temperature Hiyama cross-couplings of arylsilanes with alkyl bromides and iodides.
|
J Am Chem Soc
|
2003
|
0.80
|
|
99
|
Catalytic asymmetric cycloaddition of ketenes and nitroso compounds: enantioselective synthesis of alpha-hydroxycarboxylic acid derivatives.
|
Angew Chem Int Ed Engl
|
2009
|
0.80
|
|
100
|
NICKEL-CATALYZED ASYMMETRIC NEGISHI CROSS-COUPLINGS OF RACEMIC SECONDARY ALLYLIC CHLORIDES WITH ALKYLZINCS: (S,E)-ETHYL 6-(1,3-DIOXOLAN-2-YL)-4-METHYLHEX-2-ENOATE.
|
Organic Synth
|
2010
|
0.80
|
|
101
|
Ligands for palladium-catalyzed cross-couplings of alkyl halides: use of an alkyldiaminophosphane expands the scope of the Stille reaction.
|
Angew Chem Int Ed Engl
|
2003
|
0.79
|
|
102
|
1,2-azaborolyls, isoelectronic analogues of the ubiquitous cyclopentadienyl ligand: synthesis of B-heteroatom-substituted 1,2-azaborolyl complexes and an assessment of their electronic features.
|
Angew Chem Int Ed Engl
|
2002
|
0.77
|
|
103
|
Catalytic enantioselective synthesis of beta-lactams: intramolecular Kinugasa reactions and interception of an intermediate in the reaction cascade.
|
Angew Chem Int Ed Engl
|
2003
|
0.77
|
|
104
|
Highly enantioselective desymmetrization of anhydrides by carbon nucleophiles: reactions of Grignard reagents in the presence of (-)-sparteine.
|
Angew Chem Int Ed Engl
|
2002
|
0.77
|
|
105
|
Rhodium-catalyzed synthesis of cyclohexenones via a novel [4 + 2] annulation.
|
Org Lett
|
2002
|
0.77
|
|
106
|
Copper-catalyzed asymmetric [4+1] cycloadditions of enones with diazo compounds to form dihydrofurans.
|
J Am Chem Soc
|
2007
|
0.75
|
|
107
|
Stereoselective phosphine-catalyzed synthesis of highly functionalized diquinanes.
|
Angew Chem Int Ed Engl
|
2010
|
0.75
|
|
108
|
SYNTHESIS OF CHIRAL PYRIDINE BIS(OXAZOLINE) LIGANDS FOR NICKEL-CATALYZED ASYMMETRIC NEGISHI CROSS-COUPLINGS OF SECONDARY ALLYLIC CHLORIDES WITH ALKYLZINCS: 2,6-BIS[(4S)-4,5-DIHYDRO-4-(2-PHENYLETHYL)-2-OXAZOLYL]-PYRIDINE.
|
Organic Synth
|
2010
|
0.75
|
|
109
|
Photoinduced, Copper-Catalyzed Alkylation of Amines: A Mechanistic Study of the Cross-Coupling of Carbazole with Alkyl Bromides.
|
J Am Chem Soc
|
2017
|
0.75
|
|
110
|
Copper-catalyzed enantioselective conjugate addition of diethylzinc to acyclic enones in the presence of planar-chiral phosphaferrocene-oxazoline ligands.
|
Org Lett
|
2002
|
0.75
|
|
111
|
Synthesis, resolution, and aldol reactions of a planar-chiral Lewis acid complex.
|
J Am Chem Soc
|
2005
|
0.75
|