Catalysts
Catalytic transformations have become a mainstay in the toolkit of the synthetic and increasing non-synthetic chemist alike. We offer a wide variety of heterogeneous metal catalysts, homogeneous metal catalysts, photocatalysts, and organocatalysts. In addition to different catalyst types, we offer reaction-specific catalysts, including Baran Diversinates™ for C–H activation; Stille, Buchwald–Hartwig, Negishi, Heck, Miyaura–Suzuki, and Sonogashira for cross-coupling reactions; and Grubbs catalysts for olefin metathesis.
Cross-coupling Catalysts
We offer an extensive portfolio of nickel and palladium catalysts to aid in the creation of C-C, C-N, and C-O bonds through common cross-coupling reactions.
Buchwald Catalysts and Ligands
Buchwald Catalysts and Ligands are highly active and versatile palladium precatalysts and biarylphosphine ligands used in cross-coupling reactions for the formation of C-C, C–N, C–O, C–F, C–CF3, and C–S bonds.
Explore More Categories
Increase the rate of your reactions with our unparalleled portfolio of transition metal catalysts for your organic and organometallic chemistry breakthroughs.
Our unparalleled portfolio of C–H activation catalysts, auxiliaries, and oxidants provide reliable and predictable conversions of C–H bonds to C–C, C–N, C–O or C–X bonds.
Our diverse portfolio of phosphine ligands includes monodentate, bidentate, chiral ligands, Buchwald, cataCXium® and Dalphos ligands for applications such as Negishi, Suzuki, Stille, Heck, Sonogashira, and Buchwald-Hartwig cross-coupling.
Photocatalysis utilizes visible light to activate a chemical reaction. Our extensive portfolio of catalysts and photoreactors enable consistent reactions in photoredox catalysis.
Inorganic catalysts play a key role in many synthetic reactions in industry and academia; our unparalleled portfolio includes common heterogeneous catalysts such as platinum, palladium, ruthenium, and rhodium on carbon or silica.
Find the optimal solution in our comprehensive range of high-quality hydrogenation catalysts for all of your hydrogenation needs.
We are committed to providing unprecedented accessibility to chiral catalysts and ligands for a wide variety of C–H, C–C, C–N, and C–O bond-forming transformations.
Stock your green chemistry toolbox with our exceptional portfolio of organocatalysts for sustainable synthesis of complex molecules in small molecule drug discovery.
Our stable and tolerable NHC ligands and complexes can be used as efficient ancillary ligands to keep your work flowing in organometallic catalysis and catalysis chemistry research.
Explore our exceptional portfolio of olefin metathesis catalysts and take advantage of Grubbs’ technical expertise to advance your research and breakthrough synthesis ideas.
Shop Products
- Page 1
- Page 2
- Page 3
- Page 4
- Page 5
- Page 6
- Page 7
- Page 8
- Page 9
- Page 10
- Page 11
- Page 12
- Page 13
- Page 14
- Page 15
- Page 16
- Page 17
- Page 18
- Page 19
- Page 20
- Page 21
- Page 22
- Page 23
- Page 24
- Page 25
- Page 26
- Page 27
- Page 28
- Page 29
- Page 30
- Page 31
- Page 32
- Page 33
- Page 34
- Page 35
- Page 36
- Page 37
- Page 38
- Page 39
- Page 40
- Page 41
- Page 42
- Page 43
- Page 44
- Page 45
- Page 46
- Page 47
- Page 48
- Page 49
- Page 50
- Page 51
- Page 52
- Page 53
- Page 54
- Page 55
- Page 56
- Page 57
- Page 58
- Page 59
- Page 60
- Page 61
- Page 62
- Page 63
- Page 64
- Page 65
- Page 66
- Page 67
- Page 68
- Page 69
- Page 70
- Page 71
- Page 72
- Page 73
- Page 74
- Page 75
- Page 76
- Page 77
- Page 78
- Page 79
- Page 80
- Page 81
- Page 82
- Page 83
- Page 84
- Page 85
- Page 86
- Page 87
- Page 88
- Page 89
- Page 90
- Page 91
- Page 92
- Page 93
- Page 94
- Page 95
- Page 96
- Page 97
- Page 98
- Page 99
- Page 100
- Page 101
- Page 102
- Page 103
- Page 104
- Page 105
- Page 106
- Page 107
- Page 108
- Page 109
- Page 110
- Page 111
- Page 112
- Page 113
- Page 114
- Page 115
- Page 116
- Page 117
- Page 118
- Page 119
- Page 120
- Page 121
- Page 122
- Page 123
- Page 124
- Page 125
- Page 126
- Page 127
- Page 128
- Page 129
- Page 130
- Page 131
- Page 132
- Page 133
- Page 134
- Page 135
- Page 136
- Page 137
- Page 138
- Page 139
- Page 140
- Page 141
- Page 142
- Page 143
- Page 144
- Page 145
- Page 146
- Page 147
- Page 148
- Page 149
- Page 150
- Page 151
- Page 152
- Page 153
- Page 154
- Page 155
- Page 156
- Page 157
- Page 1
- Page 2
- Page 3
- Page 4
- Page 5
- Page 6
- Page 7
- Page 8
- Page 9
- Page 10
- Page 11
- Page 12
- Page 13
- Page 14
- Page 15
- Page 16
- Page 17
- Page 18
- Page 19
- Page 20
- Page 21
- Page 22
- Page 23
- Page 24
- Page 25
- Page 26
- Page 27
- Page 28
- Page 29
- Page 30
- Page 31
- Page 32
- Page 33
- Page 34
- Page 35
- Page 36
- Page 37
- Page 38
- Page 39
- Page 40
- Page 41
- Page 42
- Page 43
- Page 44
- Page 45
- Page 46
- Page 47
- Page 48
- Page 49
- Page 50
- Page 51
- Page 52
- Page 53
- Page 54
- Page 55
- Page 56
- Page 57
- Page 58
- Page 59
- Page 60
- Page 61
- Page 62
- Page 63
- Page 64
- Page 65
- Page 66
- Page 67
- Page 68
- Page 69
- Page 70
- Page 71
- Page 72
- Page 73
- Page 74
- Page 75
- Page 76
- Page 77
- Page 78
- Page 79
- Page 80
- Page 81
- Page 82
- Page 83
- Page 84
- Page 85
- Page 86
- Page 87
- Page 88
- Page 89
- Page 90
- Page 91
- Page 92
- Page 93
- Page 94
- Page 95
- Page 96
- Page 97
- Page 98
- Page 99
- Page 100
- Page 101
- Page 102
- Page 103
- Page 104
- Page 105
- Page 106
- Page 107
- Page 108
- Page 109
- Page 110
- Page 111
- Page 112
- Page 113
- Page 114
- Page 115
- Page 116
- Page 117
- Page 118
- Page 119
- Page 120
- Page 121
- Page 122
- Page 123
- Page 124
- Page 125
- Page 126
- Page 127
- Page 128
- Page 129
- Page 130
- Page 131
- Page 132
- Page 133
- Page 134
- Page 135
- Page 136
- Page 137
- Page 138
- Page 139
- Page 140
- Page 141
- Page 142
- Page 143
- Page 144
- Page 145
- Page 146
- Page 147
- Page 148
- Page 149
- Page 150
- Page 151
- Page 152
- Page 153
- Page 154
- Page 155
- Page 156
- Page 157
To continue reading please sign in or create an account.
Don't Have An Account?