Production Method 1

108-85-0

73183-34-3

87100-15-0

Reaction Conditions

1.1 Catalysts: (T-4)-Chlorotris(triphenylphosphine)cobalt ,  1,3-Dicyclohexyl-1,3-dihydro-2H-imidazol-2-ylidene Solvents: tert-Butyl methyl ether ;  0.5 h, rt
1.2 Reagents: Sodium ethoxide ;  16 h, 50 °C
1.3 Reagents: Oxygen

Reference

Cobalt(I)-Catalyzed Borylation of Unactivated Alkyl Bromides and Chlorides

Verma, Piyush Kumar; et al, Organic Letters, 2020, 22(4), 1431-1436

Production Method 2

24388-23-6

87100-15-0

Reaction Conditions

1.1 Reagents: Pinacol ,  Diboronic acid Catalysts: Bis[(1,2,5,6-η)-1,5-cyclooctadiene]di-μ-hydroxydirhodium Solvents: Ethanol ;  18 h, 50 °C

Reference

Mild and Selective Rhodium-Catalyzed Transfer Hydrogenation of Functionalized Arenes

Wang, Yuhan; et al, Organic Letters, 2021, 23(5), 1910-1914

Production Method 3

626-62-0

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: Potassium tert-butoxide Catalysts: Dopamine (anchored on ferrite) ,  Copper (nano-Fe-DOPA supported) Solvents: Dimethylformamide ;  18 h, rt

Reference

Efficient synthesis of alkylboronic esters via magnetically recoverable copper nanoparticle-catalyzed borylation of alkyl chlorides and bromides

Shegavi, Mahadev L.; et al, Green Chemistry, 2020, 22(9), 2799-2803

Production Method 4

25015-63-8

87100-15-0

Reaction Conditions

1.1 Catalysts: Bis(dichloro(η6-p-cymene)ruthenium) ;  24 h, rt

Reference

Ruthenium-Catalyzed Anti-Markovnikov Selective Hydroboration of Olefins

Kisan, Sesha; et al, ACS Catalysis, 2017, 7(9), 5950-5954

Production Method 5

76-09-5

108-85-0

87100-15-0

Reaction Conditions

1.1 Reagents: Tetrabutylammonium tetrafluoroborate ,  Bis(pinacolato)diborane Solvents: Dimethylacetamide ;  19 min, 25 °C
1.2 Reagents: Triethylamine ;  1 h, 25 °C
1.3 Reagents: Sodium chloride Solvents: Water ;  25 °C

Reference

Electrochemical Borylation of Alkyl Halides: Fast, Scalable Access to Alkyl Boronic Esters

Wang, Bingbing; et al, Journal of the American Chemical Society, 2021, 143(33), 12985-12991

Production Method 6

76-09-5

108-85-0

87100-15-0

Reaction Conditions

1.1 Reagents: Azobisisobutyronitrile ,  Tris(trimethylsilyl)silane ,  2,2′-Bi-1,3,2-benzodioxaborole Solvents: Dimethylacetamide ;  6 h, 80 °C; 80 °C → rt
1.2 Reagents: Triethylamine ;  1 h, rt
1.3 Reagents: Tetrabutylammonium fluoride Solvents: Diethyl ether ,  Tetrahydrofuran ;  5 min, 0 °C

Reference

Transition metal- and light-free radical borylation of alkyl bromides and iodides using silane

Sun, Beiqi; et al, Chemical Communications (Cambridge, 2021, 57(46), 5674-5677

Production Method 7

76-09-5

126812-30-4

87100-15-0

Reaction Conditions

1.1 Reagents: Tetrabutylammonium tetrafluoroborate ,  2,2′-Bi-1,3,2-benzodioxaborole Solvents: Dimethylformamide ;  4 h, rt
1.2 Reagents: Triethylamine ;  2 h, rt

Reference

Electrochemically promoted decarboxylative borylation of alkyl N-hydroxyphthalimide esters

Dai, Jian-Jun ; et al, Chinese Chemical Letters, 2022, 33(3), 1555-1558

Production Method 8

76-09-5

87100-15-0

Reaction Conditions

1.1 Reagents: 2,2′-Bi-1,3,2-benzodioxaborole Catalysts: 2,4,6-Tris(diphenylamino)-3,5-difluorobenzonitrile Solvents: Dimethylformamide ;  6 h, 20 °C
1.2 Reagents: Triethylamine ;  6 h, rt

Reference

Light-Mediated Sulfur-Boron Exchange

Panferova, Liubov I.; et al, Organic Letters, 2021, 23(10), 3919-3922

Production Method 9

542-18-7

73183-34-3

87100-15-0

Reaction Conditions

1.1 Catalysts: Cupric chloride ,  1,3-Bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-ylidene Solvents: Tetrahydrofuran ;  10 min, rt
1.2 Reagents: Potassium methoxide ;  10 min, rt
1.3 30 min, 60 °C

Reference

Highly efficient synthesis of alkylboronate esters via Cu(II)-catalyzed borylation of unactivated alkyl bromides and chlorides in air

Bose, Shubhankar Kumar; et al, ACS Catalysis, 2016, 6(12), 8332-8335

Production Method 10

931-50-0

25015-63-8

87100-15-0

Reaction Conditions

1.1 Solvents: Tetrahydrofuran ;  1 h, 25 °C
1.2 Reagents: Hydrochloric acid Solvents: Water

Reference

Hydride as a Leaving Group in the Reaction of Pinacolborane with Halides under Ambient Grignard and Barbier Conditions. One-Pot Synthesis of Alkyl, Aryl, Heteroaryl, Vinyl, and Allyl Pinacolboronic Esters

Clary, Jacob W.; et al, Journal of Organic Chemistry, 2011, 76(23), 9602-9610

Production Method 11

76-09-5

87100-15-0

Reaction Conditions

1.1 Reagents: 2,2′-Bi-1,3,2-benzodioxaborole Catalysts: Cupric chloride Solvents: Acetonitrile ;  10 h, rt
1.2 16 h, 40 °C
1.3 Reagents: Triethylamine Solvents: Dichloromethane ;  1 h, rt

Reference

Copper-Mediated Dehydrogenative C(sp3)-H Borylation of Alkanes

Sang, Ruocheng ; et al, Journal of the American Chemical Society, 2023, 145(28), 15207-15217

Production Method 12

1632411-83-6

108-85-0

87100-15-0

Reaction Conditions

1.1 Catalysts: Ferrous bromide ,  Dibromo[1,1′-oxybis[ethane]]magnesium Solvents: Tetrahydrofuran ;  1 h, rt

Reference

Iron-Catalyzed Borylation of Alkyl, Allyl, and Aryl Halides: Isolation of an Iron(I) Boryl Complex

Bedford, Robin B.; et al, Organometallics, 2014, 33(21), 5940-5943

Production Method 13

1632411-83-6

626-62-0

87100-15-0

Reaction Conditions

1.1 Catalysts: Ferrous bromide ,  Dibromo[1,1′-oxybis[ethane]]magnesium Solvents: Tetrahydrofuran ;  1 h, rt

Reference

Iron-Catalyzed Borylation of Alkyl, Allyl, and Aryl Halides: Isolation of an Iron(I) Boryl Complex

Bedford, Robin B.; et al, Organometallics, 2014, 33(21), 5940-5943

Production Method 14

76-09-5

14874-70-5

47645-89-6

87100-15-0

Reaction Conditions

1.1 Reagents: 2,2′-Bi-1,3,2-benzodioxaborole Solvents: Dimethylacetamide ;  6 h, 30 °C
1.2 Reagents: Triethylamine ;  1 h, rt

Reference

Deaminative Borylation of Aliphatic Amines Enabled by Visible Light Excitation of an Electron Donor-Acceptor Complex

Sandfort, Frederik; et al, Chemistry - A European Journal, 2018, 24(65), 17210-17214

Production Method 15

76-09-5

87100-15-0

Reaction Conditions

1.1 Reagents: 2,2′-Bi-1,3,2-benzodioxaborole Catalysts: Tris[2-[4-(1,1-dimethylethyl)-2-pyridinyl-κN]-3,5-difluorophenyl-κC]iridium Solvents: Ethyl acetate ,  Hexamethylphosphoramide ;  14 h, rt
1.2 Reagents: Triethylamine ;  1 h, rt

Reference

Decarboxylative Borylation of Stabilized and Activated Carbon Radicals

Zhang, Qiang; et al, Angewandte Chemie, 2020, 59(49), 21875-21879

Production Method 16

76-09-5

87100-15-0

Reaction Conditions

1.1 Reagents: Diisopropylethylamine ,  Boron tribromide Solvents: Dichloromethane ;  0 °C; 12 - 48 h, rt
1.2 Reagents: Triethylamine Solvents: Dichloromethane ;  1 h, rt

Reference

Site-Fixed Hydroboration of Terminal and Internal Alkenes using BX3/iPr2NEt

Li, Sida; et al, Angewandte Chemie, 2021, 60(50), 26238-26245

Production Method 17

73183-34-3

87100-15-0

78782-17-9

94242-85-0

25015-63-8

Reaction Conditions

1.1 Catalysts: Rhodium, [(1,2,3,4,5,6-η)-hexamethylbenzene][(1,2,3,4,5-η)-1,2,3,4,5-pentamethyl… Solvents: Cyclohexane ;  14 h, 3500 kPa, 150 °C

Reference

Catalyst-controlled selectivity in the C-H borylation of methane and ethane

Cook, Amanda K.; Schimler, Sydonie D.; Matzger, Adam J.; Sanford, Melanie S., Science (Washington, 2016, 351(6280), 1421-1424

Production Method 18

25015-63-8

87100-15-0

73183-34-3

Reaction Conditions

1.1C:2094503-97-4, C:Et3BH ?Na, S:THF, 2 min, rt
1.224 h, 100°C

Reference

Cobalt-Catalyzed Regioselective Borylation of Arenes: N-Heterocyclic Silylene as an Electron Donor in the Metal-Mediated Activation of C-H Bonds

By Ren, Hailong et al, Chemistry - A European Journal, 2017, 23(24), 5663-5667

Production Method 19

76-09-5

4441-56-9

87100-15-0

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: 1,4-Dioxane ;  5 h, 100 °C; 100 °C → rt
1.2 10 min, 100 °C

Reference

A practical and modular construction of C(sp3)-rich alkyl boron compounds

Yang, Yangyang; et al, ChemRxiv, 2020, 1, 1-9

Production Method 20

76-09-5

4441-56-9

87100-15-0

Reaction Conditions

1.1 3 h, rt

Reference

Hydrogenation of Borylated Arenes

Wollenburg, Marco; et al, Angewandte Chemie, 2019, 58(20), 6549-6553

Production Method 21

76-09-5

4441-56-9

87100-15-0

Reaction Conditions

1.1 Reagents: Sulfuric acid magnesium salt (1:1) Solvents: Diethyl ether ;  16 h, rt

Reference

Synthesis of 3-Aryl-1-aminopropane Derivatives: Lithiation-Borylation-Ring-Opening of Azetidinium Ions

Casoni, Giorgia; et al, Synthesis, 2016, 48(19), 3241-3253

Production Method 22

108-85-0

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: Potassium methoxide Catalysts: Copper Solvents: Dimethylformamide ;  1 h, rt

Reference

Facile synthesis of alkyl- and arylboronate esters enabled by a carbon nanotube supported copper catalyst

Saini, Suresh; et al, Catalysis Science & Technology, 2023, 13(1), 147-156

Production Method 23

108-85-0

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: Potassium tert-butoxide Catalysts: Dopamine (anchored on ferrite) ,  Copper (nano-Fe-DOPA supported) Solvents: Dimethylformamide ;  18 h, rt

Reference

Efficient synthesis of alkylboronic esters via magnetically recoverable copper nanoparticle-catalyzed borylation of alkyl chlorides and bromides

Shegavi, Mahadev L.; et al, Green Chemistry, 2020, 22(9), 2799-2803

Production Method 24

24388-23-6

87100-15-0

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: [1-[2,6-Bis(1-methylethyl)phenyl]-3,3,5,5-tetramethyl-2-pyrrolidinylidene]chloro… Solvents: 2,2,2-Trifluoroethanol ;  24 h, 5 MPa, rt

Reference

Hydrogenation of (Hetero)aryl Boronate Esters with a Cyclic (Alkyl)(amino)carbene-Rhodium Complex: Direct Access to cis-Substituted Borylated Cycloalkanes and Saturated Heterocycles

Ling, Liang; et al, Angewandte Chemie, 2019, 58(20), 6554-6558

Production Method 25

626-62-0

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: Potassium methoxide Catalysts: Copper Solvents: Dimethylformamide ;  1 h, rt

Reference

Facile synthesis of alkyl- and arylboronate esters enabled by a carbon nanotube supported copper catalyst

Saini, Suresh; et al, Catalysis Science & Technology, 2023, 13(1), 147-156

Production Method 26

626-62-0

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: 2,2′-Bi-1,3,2-benzodioxaborole Solvents: Dimethylformamide ;  24 h, rt
1.2 Reagents: Triethylamine ;  1 h, rt

Reference

Metal-Free Radical Borylation of Alkyl and Aryl Iodides

Cheng, Ying; et al, Angewandte Chemie, 2018, 57(51), 16832-16836

Production Method 27

25015-63-8

87100-15-0

Reaction Conditions

1.1 Catalysts: 2839130-42-4 ;  12 h, 100 °C

Reference

Monomeric Magnesium Catalyzed Alkene and Alkyne Hydroboration

Kumar, Rohit; et al, Chemistry - A European Journal, 2022, 28(56),

Production Method 28

25015-63-8

87100-15-0

Reaction Conditions

1.1 Catalysts: 1,2-Bis(diphenylphosphino)ethane ,  Di-μ-chlorobis[(1,2,5,6-η)-1,5-cyclooctadiene]diiridium Solvents: Dichloromethane ;  0 °C; 16 h, rt
1.2 Reagents: Methanol ,  Water ;  rt

Reference

A General Approach to Deboronative Radical Chain Reactions with Pinacol Alkylboronic Esters

Andre-Joyaux, Emy; et al, Angewandte Chemie, 2020, 59(33), 13859-13864

Production Method 29

73183-34-3

87100-15-0

Reaction Conditions

1.1 Catalysts: 1,10-Phenanthroline ,  Cuprous iodide Solvents: Acetonitrile ;  0.5 h, 50 °C; 50 °C → rt

Reference

Synthesis of Functionalized Organoboron/Silicon Compounds by Copper-Catalyzed Coupling of Alkylsilyl Peroxides and Diboron/Silylborane Reagents

Seihara, Takumi; et al, Organic Letters, 2019, 21(7), 2477-2481

Production Method 30

76-09-5

626-62-0

87100-15-0

Reaction Conditions

1.1 Reagents: Tetrabutylammonium tetrafluoroborate ,  Bis(pinacolato)diborane Solvents: Dimethylformamide ;  12 min, 25 °C
1.2 Reagents: Triethylamine ;  1 h, 25 °C
1.3 Reagents: Sodium chloride Solvents: Water ;  25 °C

Reference

Electrochemical Borylation of Alkyl Halides: Fast, Scalable Access to Alkyl Boronic Esters

Wang, Bingbing; et al, Journal of the American Chemical Society, 2021, 143(33), 12985-12991

Production Method 31

542-18-7

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: Potassium tert-butoxide Catalysts: Cuprous chloride ,  1,1′-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis[1,1-diphenylphosphine] Solvents: Tetrahydrofuran ;  rt; rt; 18 h, rt

Reference

Copper(I)-Catalyzed Boryl Substitution of Unactivated Alkyl Halides

Ito, Hajime; et al, Organic Letters, 2012, 14(3), 890-893

Production Method 32

542-18-7

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: Lithium tert-butoxide Catalysts: Copper, compd. with palladium (2.8:0.2) (graphene supported) Solvents: Dimethylformamide ;  2 h, 50 °C

Reference

Visible-light-driven graphene supported Cu/Pd alloy nanoparticle-catalyzed borylation of alkyl bromides and chlorides in air

Jiao, Zhi-Feng; et al, Journal of Catalysis, 2021, 395, 258-265

Production Method 33

76-09-5

87100-15-0

Reaction Conditions

1.1 Reagents: Cupric chloride ,  2,2′-Bi-1,3,2-benzodioxaborole Solvents: Acetonitrile ;  18 h, rt
1.2 Reagents: Triethylamine ;  4 h, rt

Reference

Photoinduced C(sp3)-H borylation of alkanes mediated by copper(II) chloride

Fang, Wen; et al, Chemical Communications (Cambridge, 2023, 59(46), 7108-7111

Production Method 34

73183-34-3

87100-15-0

Reaction Conditions

1.1 Catalysts: Bis(1,5-cyclooctadiene)nickel ,  Tri-tert-butylphosphine Solvents: Methanol ,  Toluene ;  10 h, 75 °C

Reference

Base-free nickel-catalyzed hydroboration of simple alkenes with bis(pinacolato)diboron in an alcoholic solvent

Li, Jiang-Fei; et al, Green Chemistry, 2017, 19(19), 4498-4502

Production Method 35

73183-34-3

87100-15-0

Reaction Conditions

1.1 Reagents: Potassium tert-butoxide Catalysts: 2659230-20-1 Solvents: Acetonitrile ,  Water ;  6 h, rt

Reference

Copper-Photocatalyzed Hydroboration of Alkynes and Alkenes

Zhong, Mingbing; et al, Angewandte Chemie, 2021, 60(26), 14498-14503

Production Method 36

76-09-5

14874-70-5

47645-89-6

87100-15-0

Reaction Conditions

1.1 Reagents: 2,2′-Bi-1,3,2-benzodioxaborole Solvents: Dimethylacetamide ;  14 h, rt
1.2 Reagents: Triethylamine ;  1 h, rt

Reference

Photoinduced Deaminative Borylation of Alkylamines

Wu, Jingjing; et al, Journal of the American Chemical Society, 2018, 140(34), 10700-10704

Production Method 37

76-09-5

14874-70-5

47645-89-6

87100-15-0

Reaction Conditions

1.1 Reagents: 2,2′-Bi-1,3,2-benzodioxaborole Catalysts: 4,4′-Bis(1,1-dimethylethyl)-2,2′-bipyridine Solvents: Dimethylacetamide ;  6 h, 100 °C; 100 °C → rt
1.2 Reagents: Triethylamine ;  1 h, rt

Reference

Selective C-N Borylation of Alkyl Amines Promoted by Lewis Base

Hu, Jiefeng; et al, Angewandte Chemie, 2018, 57(46), 15227-15231

Production Method 38

76-09-5

87100-15-0

Reaction Conditions

1.1 Reagents: Pyridine-borane ,  Iodine Solvents: Dichloromethane ;  0 °C; 0 °C → rt
1.2 2 h, rt; rt → 0 °C
1.3 Reagents: Sodium hydroxide Solvents: Water ;  0 °C → rt
1.4 Solvents: Dichloromethane ;  15 h, rt

Reference

Formation of Pinacol Boronate Esters via Pyridine Iodoborane Hydroboration

Karatjas, Andrew G.; et al, Journal of Organic Chemistry, 2008, 73(23), 9508-9510

Production Method 39

76-09-5

87100-15-0

Reaction Conditions

1.1 Reagents: N,N-Diethyl-2-propanamine ,  Boron tribromide Solvents: Dichloromethane ;  0 °C; 12 h, rt
1.2 Reagents: Triethylamine Solvents: Dichloromethane ;  1 h, rt

Reference

Site-fixed hydroboration of alkenes under metal-free conditions: scope and mechanistic studies

Li, Sida; et al, ChemRxiv, 2021, 1, 1-15

Production Method 40

87100-15-0

Reaction Conditions

1.1 Reagents: Sodium tert-butoxide Solvents: Tetrahydrofuran ;  3 h, rt

Reference

Simple access to elusive α-boryl carbanions and their alkylation: an umpolung construction for organic synthesis

Hong, Kai; et al, Journal of the American Chemical Society, 2014, 136(30), 10581-10584

2-Cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Raw materials

• chlorocyclohexane
• 2,3-Dimethylbutane-2,3-diol
• Cyclohexylboronic acid
• Borate(1-),tetrafluoro-
• Borate(1-), [2,3-dimethyl-2,3-butanediolato(2-)-κO2,κO3](1,1-dimethylethyl)(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, lithium (1:1), (T-4)-
• Bromocyclohexane
• Cyclohexylmagnesium Bromide (~1.0 M in THF)
• Iodocyclohexane
• Bis(pinacolato)diborane
• Pinacolborane
• Phenylboronic Acid Pinacol Ester
• PYRIDINIUM, 1-CYCLOHEXYL-2,4,6-TRIPHENYL-
• 2-[(Cyclohexylcarbonyl)oxy]-1H-isoindole-1,3(2H)-dione

2-Cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Preparation Products

• Bis[(pinacolato)boryl]methane (78782-17-9)
• 2,4,4,5,5-Pentamethyl-1,3,2-dioxaborolane (94242-85-0)
• 2-Cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (87100-15-0)
• Bis(pinacolato)diborane (73183-34-3)
• Pinacolborane (25015-63-8)

• 1. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
  Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
• 2. Establishing the accuracy of position-specific carbon isotope analysis of propane by GC-pyrolysis-GC-IRMS
  ChangjieLiu,PengLiu,XiaofengWang,XiaoqiangLi,JuskeHorita
• 3. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?
  Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
• 4. Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation
  Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
• 5. Excellent kinetics of single-phase Gd-doped ceria fuel electrodes in solid oxide cells?
  Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Boronic acid derivatives Boronic acid esters
• Other Chemical Reagents Derivatization Reagents
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

• 1357000-40-8(1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1R,2R,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]-)
• 1613405-35-8(1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1R,2S,3R,5R)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-)
• 167692-95-7(2-Cyclohexylethylboronic acid pinacol ester)
• 931583-43-6(Cycloheptylboronic acid, pinacol ester)
• 1218790-09-0(trans-Cyclohexane-1,2-diboronic Acid Pinacol Ester)
• 1613405-34-7(1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1S,2R,3S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-yl]-)
• 126689-02-9(1,3,2-Dioxaborolane, 2-[(1R,2R)-2-butylcyclopropyl]-4,4,5,5-tetramethyl-, rel-)
• 737776-93-1(Ferrocene,1,1'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-)
• 66217-55-8(1,3,2-DIOXABOROLANE, 2-CYCLOPENTYL-4,4,5,5-TETRAMETHYL-)
• 30882-57-6((3R,5R,5'S,8R,9S,10S,13S,14S,17R)-2'-Cyclohexyl-5',10,13-trimethylspiro[1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthrene-17,4'-1,3,2-dioxaborolane]-3-ol)