Organoboranes

<p>Applications trans-Campestanyl 3-(4-(tert-Butyldimethylsilyl)oxy)-ferulate is an intermediate used in the synthesis of trans-Campestanyl Ferulate (C155308), which is used for synthesis of trans-feruloyl-β-sitostanol.<br>References Condo, A., et al.: J. Agric. Food Chem., 49, 4961 (2001);<br></p>

<p>Stability Hygroscopic<br>Applications 2-(4-ethenylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane<br></p>

<p>Applications 3-(Cyclopropylaminocarbonyl)phenylboronic acid<br></p>

<p>Applications 4-Carboxyphenylboronic acid is a reagent used in suzuki coupling reactions.<br>References Hu, Z., et al.: Wuji Huaxue Xuebao, 34, 387 (2018); Ibrahim, M., et al.: J. Organomet. Chem., 859, 44 (2018); Erami, R. S., et al.: Catalysts, 7, 76 (2017)<br></p>

<p>Applications 4-(Methoxycarbonyl)phenylboronic Acid is used in the synthesis and evaluation of several organic compounds including that of 4-Cyclohexylbutyl-N-[(S)-2-oxoazetidin-3-yl]carbamate which is a potent inhibitor of intracellular NAAA activity. Also used in the design and synthesis of BMS-955176 which is a potent, orally active second generation HIV-1 maturation inhibitor.<br>References Nuzzi, A., et al.: Eur. J. Med. Chem., 111, 138 (2016); Rogueiro-Ren, A., et al.: ACS Med. Chem. Lett., 7, 568 (2016);<br></p>

<p>Applications 5-Formylfuran-2-boronic Acid Neopentyl Glycol Ester is a useful reagent in lapatinib synthesis.<br>References Radl, S., et al.: PCT Int. Appl. (2014), WO 2014059956 A1<br></p>

<p>Applications Benzo[b]thien-3-ylboronic acid is used in the synthesis and evaluation of dual wavelength fluorescent benzo[b]thiophene boronic acid derivatives for sugar/glycoprotein sensing.<br>References Akay, S., et al.: Chem. Biol. Drug Des., 70, 279 (2007)<br></p>

<p>Applications Allylboronic acid pinacol ester<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications (2-Ethynylphenyl)boronic acid<br></p>

<p>Applications tert-Butyldimethyl(4-(nitrosophenyl)butoxy)silane is an intermediate used in the synthesis of (E)-S-(3-((4-((4-(4-hydroxybutyl)phenyl)diazenyl)phenyl)amino)-3-oxopropyl) methanesulfonothioate (H895230), which is a useful research chemical.<br></p>

<p>Applications 3-((1-Oxo-1-(3-(trimethylsilyl)propoxy)propan-2-yl)thio)propanoic acid is useful reagent for organic reactions and synthesis.<br></p>

<p>Stability Moisture Sensitive<br>Applications Chloroborane Methyl Sulfide Complex is a reagent in the synthesis of 3,4-Dimethyl-5-pentyl-2-furanundecanoic Acid (D477535); a furan fatty acid known to exhibit radical-scavenging ability and having anti-inflammatory properties.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Grahl, N., et al.: Marine. Biol., 157, 1567 (2010); Spiteller, G., et al.: Lipids., 40, 75 (2005); Wakimoto, T., et al.: PNSA., 108, 17533 (2011)<br></p>

<p>Applications Tris(trimethylsilyl)guanine is an intermediate used in the synthesis of 9-(2-Hydroxyethyl)guanine (H942035), which is an impurity of the antiviral agent Acyclovir (A192400). 9-(2-Hydroxyethyl)guanine is a nucleoside phosphotransferase acceptor.<br>References Kamimura, A. et al.: Agric. Biol. Chem., 37, 2037 (1973);<br></p>

<p>Stability Moisture Sensitive<br>Applications Chlorotriethylsilane is used in the preparation of potent silylating agent and lewis acid catalyst. Chlorotriethylsilane derivatived ethers have been shown to be more stable towards hydrolysis than are trimethyl ethers.<br> E0<br>References Alvisi, C. et al.: J. Org. Chem., 63, 1330 (1998): Higashiya, S. et al.: J. Org. Chem., 69, 6326 (2004); Hicks, J.D. et al.: Org. Lett., 9, 5621 (2007);<br></p>

<p>Applications B-(9-Phenyl-9H-carbazol-3-yl)boronic Acid is used in the synthesis of alkyl-functionalized organic dyes.<br>References Lee, E. et al.: Bull. Kor. Chem. Soc., 33, 293 (2012);<br></p>

<p>Applications 3-Formylphenylboronic Acid is a reactant in the synthesis of I-BET726 (GSK1324726A), a potent tetrahydroquinoline ApoA1 up-regulator and selective BET bromodomain inhibitor.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Gosmini, R., et. al.: J. Med. Chem., 57, 8111 (2014)<br></p>

<p>Applications Trimethylsilylethynyl(phenyl)iodonium Tetrafluoroborate is used in synthesis of 1-Alkynyl(triphenyl)arsonium Tetrafluoroborates by onium transfer reaction of 1-Alkynyl(phenyl)iodonium Tetrafluoroborates with Triphenylarsine. Also, used in preparation of Furan- and Thiophene-substituted alkynes and alkynyl ketones by Copper Iodide-catalyzed coupling and carbonylation of Heterocyclic Boronic Acids with Alkynyliodonium salts.<br>References Nagaoka, T., et al.: Tetrah. Lett., 36, 261-4 (1995); Yu, Chan-Mo, et al.: Synlett, 2631-2634 (2005);<br></p>

<p>Applications (2,5-Dimethylphenyl)boronic Acid is a useful synthetic intermediate. It can be used to prepare fluorenones/indenofluorenediones.<br>References Liu, T., et al.: Org. Lett., 13, 2452 (2011)<br></p>

<p>Applications Methoxy4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-benzenemethanol, is prepared synthetically from vanillin (V097500) with an intermediate of methoxy-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-benzaldehyde (M269710).<br>References Gowravarm, S. et al.: Adv. Synth. Catal., 343, 169 (2001)<br></p>

<p>Applications 2-(6,6-Dimethyl-1-cyclohexen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane was used in the preparation of conformationally constrained cyclic carboxylic acid derivatives useful as GPR40 modulators for treating metabolic disorders.<br></p>

<p>Applications Isopropenylboronic Acid Pinacol Ester, can be used as an intermediate in the synthesis of variety of cyclic and acyclic organic compounds. It is also shown that the α-Substituted Allyl/Croty of this compound can be used for highly Diastereo- and Enantioselective allylboration of aldehydes.<br>References Salaun, J. et al.: Topics in Curr. Chem. 1, 144 (1988); Chen, J. et al.: J. Amer. Chem. Soci., 135, 5316 (2013);<br></p>

<p>Stability Volatile<br>Applications Allyltrimethylsilane is used in the allylation of aldehydes, imines, allylic and benzylic alcohols, and chiral α-keto-amides that are derived from (S)-proline esters.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Yadav, J.S., et al.: Tetrahedron Lett., 43, 3783 (2002); Aggarwal, V.K., et al.: Tetrahedron Lett., 37, 3745 (1996); Wang, D.K., et al.: J. Org. Chem., 64, 4233 (1999); Kaur, G., et al.: Tetrahedron Lett., 38, 2521 (1997); Soai, K., et al.: J. Chem. Soc., Chem. Commun., 15, 1016 (1984)<br></p>

<p>Applications 2,6-Dimethylphenylboronic acid<br></p>

<p>Applications Thiazol-4-ylboronic acid (cas# 1016642-07-1) is a useful research chemical.<br></p>

<p>Applications Trichloro[2-(chloromethyl)-2-propen-1-yl]silane is an intermediate used in the synthesis of 2-​(Chloromethyl)​allyl-​trimethylsilane (C371430), which is one of the reagents to synthesize Leucasandrolide A Macrolide (I) via Mukaiyama aldol coupling.2-​(Chloromethyl)​allyl-​trimethylsilane was used in catalytic Sakurai reaction of α,​β-​enones.<br>References Kopecky, D., et al.: J. Am. Chem. Soc., 123, 8420 (2001).Lee, P., et al.: J. Org. Chem., 66, 8646 (2001).<br></p>

<p>Applications 4-Ethylsulfonylphenylboronic acid is used in the discovery of small molecular RIP1 kinase inhibitors for the treatment of pathologies associated with necroptosis.<br>References Harris, P. A,, et al.: ACS Med. Chem. Lett., 4, 1238 (2013)<br></p>

<p>Applications Tetramethylammonium Tetrafluoroborate (cas# 661-36-9) is a useful research chemical.<br></p>

<p>Applications 1,2,2-Trimethylcyclopropyl Boronic Acid is the boronic acid analogue of 1,2,2-Trimethylcyclopropane. Boronic acid derivatives are widely used in several applications in organic synthesis.<br></p>

<p>Applications Perphenylcyclopentasilane is an intermediate in the synthesis of Cyclopentasilane (C988380), a reagent used for depositing silicon on surfaces for electronics applications.<br>References Morisaki, Y., et al.: Chem. Lett., 38, 498 (2009);<br></p>

<p>Applications tert-Butyl (5-Chloro-2-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate is used as a reactant in the synthesis of BRAF-kinase inhibitors.<br>References Repik, Alexey E., et al.: PCT Int. Appl., WO 2017146604 A1 20170831 (2017)<br></p>

<p>Applications 5-Ethyl-2-fluorophenylboronic acid<br></p>

<p>Applications TRIMETHYL(BROMODIFLUOROMETHYL)SILANE (cas# 115262-01-6) is a useful research chemical.<br></p>

<p>Applications 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopent-2-en-1-one (cas# 1370008-65-3) is a useful research chemical.<br></p>

<p>Applications 1,1,3,3-Tetramethyldisiloxane is an organosilane reducing agent and can be used in several reduction reactions including reductive formation of sulfides and reductive etherification.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Pesti, J., et al.: Org. Process Res. Dev., pages ahead of print (2016);<br></p>

<p>Stability Volatile<br>Applications Methoxytrimethylsilane (cas# 1825-61-2) is a useful research chemical.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>Applications 2-tert-Butyldimethylsilyloxyethyl Tosylate is an intermediate in the synthesis of Everolimus (E945400), which is Everolimus Macrolide immunosuppressant; Everolimus is a derivative of Rapamycin. Everolimus inhibits cytokine-mediated lymphocyte proliferation.<br>References Dumont, F.J., et al.: Curr. Opin. Invest. Drugs, 2, 1220 (2001), Kovarik, J. M., et al.: Clin. Pharmacol. Ther., 69, 48 (2001), Nashan, B., et al.: Ther. Drug Monit., 24, 53 (2002),<br></p>

<p>Applications Dibenzothiophene-2-boronic acid is a useful reagent for organic synthesis and other chemical processes.<br>References Duncton, M. A. J., et al.: Org. Lett., 10, 3259 (2008)<br></p>

<p>Applications 3-Acetylphenylboronic acid<br></p>

<p>Stability Hygroscopic<br>Applications Methyl (3R)-3-(tert-Butyldimethylsilanyloxy)-5-oxo-6-(triphenylphosphanylidene)hexanoate was used to preapre pyrimidinyl- and pyrrolylheptenoates with HMG-CoA reductase inhibitory activities.<br>References Watanabe, M., et al.: Bioorg. Med. Chem., 5, 437 (1997); Pfefferkorn, J., et al.: J. Med. Chem., 51, 31 (2008);<br></p>

<p>Applications 2-Hydroxyphenylboronic acid<br></p>

<p>Applications 5-Bromopentylboronic Acid<br></p>

<p>Applications Ethynylboronic Acid MIDA Ester is a useful reagent in preparatino of borono-substited 1(2H)-isoquinolinones by rhodium-catalyzed cycloaddition.<br>References Wang, H., et al.: J. Am. Chem. Soc., 134, 19592 (2012);<br></p>

<p>Applications 5-Formylfuran-2-boronic Acid Pinacol Ester could be useful for the diastereoselective synthesis of cyclic peptide macrocycles via Petasis borono-Mannich reaction<br>References Yamaguchi, A., et al.: Chem. Commun. (Cambridge, U. K.), 55, 10567 (2019)<br></p>

<p>Applications 5-(Ethoxycarbonyl)thiophene-3-boronic Acid is a useful reagent for preparing hydroxyimino(phenyl)propanones as GPBAR1 agonists.<br>References Bissantz, C., et al.: U.S. Pat. Appl. Publ. (2012), US 20120010190 A1<br></p>

<p>Applications 5-Aminoboronphthalide is used as a reactant in the preparation of 2,1-benzoxaborole peptide isoquinoline derivatives as HCV NS3 protease inhibitors. It is also used as reactant in the synthesis of nanocarrier for chemomechanically driven guest delivery fueled by intracellular ATP.<br>References Li, X., et al.: Bioorg. Med. Chem. Lett., 21, 2048 (2011); Biswas, S., et al.: Nat. Chem., 5, 613 (2013);<br></p>

<p>Stability Moisture Sensitive<br>Applications 4-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester<br></p>

<p>Please enquire for more information about 5-Methylpyridine-2-boronicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>B-chlorocatecholborane is a nonpolar solvent that is used in the synthesis of drugs and other organic compounds. It reacts with trifluoromethanesulfonic acid to form a coordination complex, which can be used to synthesize pharmaceuticals. B-chlorocatecholborane can also be used for solid-phase synthesis, which offers an efficient method for chemical reactions. This reagent has been shown to react with 5-hydroxytryptamine 4 (5-ht4) receptor, which is involved in the regulation of appetite and sleep. It also reacts with 2-arachidonoylglycerol (2AG), a lipid molecule that mediates the effects of cannabis on appetite, pain and memory. The structure of this compound was determined using nuclear magnetic resonance spectroscopy and mass spectrometry. The biological properties of B-chlorocatecholborane have not yet been studied.</p>

<p>Epsilon-Carotene is a carotenoid that is found in plants. It is synthesized from beta-carotene through the action of enzymes called beta-carotene ketolases. Epsilon-Carotene can be cleaved by enzymes to produce lycopene and beta-cryptoxanthin. The biosynthesis of Epsilon-Carotene has been studied in a number of clinical studies, including the effect on human tissues and the prevention of cancer. Epsilon-Carotene has also been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>4-Phenoxyphenylboronic acid is a chemical inhibitor of protein kinase. It binds to the ATP binding site of the enzyme and prevents ATP from binding, thereby inhibiting the phosphorylation of proteins. This inhibition blocks the activation of downstream pathways that are involved in cell proliferation, leading to apoptotic cell death. 4-Phenoxyphenylboronic acid has been shown to inhibit growth of human cancer cells in vitro. This molecule also inhibits root formation and plant growth, which may be due to its ability to selectively inhibit protein kinases found in plant cells.</p>

<p>5-Bromo-2-fluorophenyl)boronic acid is a synthetic chemical that is used in the synthesis of pharmaceuticals and pesticides. This compound is an inhibitor of bace1, which is an enzyme involved in the production of amyloid beta peptide (Aβ) and other proteins implicated in Alzheimer's disease. 5-Bromo-2-fluorophenyl)boronic acid has been shown to be effective at reducing Aβ levels in mice with Alzheimer's disease. It also inhibits pyrethroid, a pesticide that is used on crops to control insects, by binding to the active site of the enzyme. 5-Bromo-2-fluorophenyl)boronic acid has been evaluated for use as a cancer treatment, but these studies have not been completed.</p>

<p>Potassium trimethylsilanolate is a chemical substance that has inhibitory properties. It is a trifluoroacetic acid derivative that inhibits the activity of certain enzymes, such as proteases and lipases. The compound's inhibitory properties are due to its ability to bind to cytochrome cb2 receptors by means of hydrogen bonding. The binding of potassium trimethylsilanolate to the receptor prevents the activation of apoptosis proteins and protein synthesis in cells. This substance also has an inhibitory effect on water vapor, inhibiting the formation of water molecules from hydrogen atoms and oxygen atoms. Potassium trimethylsilanolate can be used as an anti-cancer agent by preventing cell division in tumor cells and preventing cancer metastasis through inhibition of protease activity.</p>

<p>Triethoxy(propyl)silane is an organosilicon compound that has reactive properties. It is a polymeric material that can be used as a component in paints, coatings, and sealants. The reaction of triethoxy(propyl)silane with sodium hydroxide solution yields hydrogen fluoride, water vapor, and hydrochloric acid. Triethoxy(propyl)silane has been shown to react with hydroxide solution to form polycarboxylic acids. The hydroxyl group on the triethoxy(propyl)silane molecule is responsible for the transport properties of this compound.</p>

<p>Please enquire for more information about 5-Fluoropyridine-2-boronic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Mercaptopropyl)trimethoxysilane is a molecule made up of three parts: a trimethoxysilane group, a trimethylsilyl group, and a mercapto group. The trimethoxysilane group is hydrophilic in nature and has an electron withdrawing effect on the molecule. The trimethylsilyl group is hydrophobic in nature and has an electron donating effect on the molecule. The mercapto group is reactive in nature and has a high redox potential. 3-Mercaptopropyl)trimethoxysilane can be used as a chemical additive to increase the stability of hydrochloric acid in water vapor by reacting with the hydroxyl groups to form stable compounds. This compound also reacts with hydrogen gas to produce methane gas, which can be used as fuel or as an alternative energy source. 3-Mercaptopropyl)trimethoxysilane also has synergistic</p>

<p>Triisopropylsilylacetylene is an aliphatic hydrocarbon with a reactive site that can be used in the synthesis of other chemical compounds. It has been shown to have an inhibitory effect on the formation of reactive oxygen species and inflammation in mice, which may be due to its ability to reduce the production of inflammatory mediators such as prostaglandin E2. Triisopropylsilylacetylene also has a hydroxyl group, which allows it to act as an anti-inflammatory agent by inhibiting the enzyme cyclooxygenase. Additionally, triisopropylsilylacetylene has a carbonyl group, which gives it aromatic properties that can be used for synthetic purposes.</p>

<p>m-Carborane is a molecule that is composed of a chlorine atom and an aromatic hydrocarbon. m-Carborane has been shown to be an estrogen receptor modulator, which may have potential as a drug for the prevention or treatment of hormone-related diseases. This compound has also been shown to act as a fluorophore and to have high melting points. It forms hydrogen bonds with other molecules and can bind to progesterone receptors, which are found in breast cancer cells. These interactions have been studied using x-ray crystal structures and microscopy studies on MCF-7 cells.</p>

<p>2-Chloro-3-ethylbenzoxazolium tetrafluoroborate is a synthetic compound that inhibits the enzyme maltase. This compound is used in the treatment of diabetic patients with intestinal maltase deficiency and has been shown to be effective in clinical studies. 2-Chloro-3-ethylbenzoxazolium tetrafluoroborate has also been shown to inhibit other enzymes, such as thiocarbamate synthetase and aminooxazoline synthetase, which are involved in the biosynthesis of chlorinated pesticides and herbicides. The chloride ion is necessary for this inhibition activity. The compound can be prepared by a preparative method that involves hexaacetate and chloride ion or by using an aglycone, trehalamine, or stereospecific method.</p>

<p>O-Benzyl psilocybin is a hydrophobic molecule with an affinity for lipase. It has been shown to exhibit growth inhibition on malignant cells in tissue culture, and has been investigated as a potential anticancer agent. O-Benzyl psilocybin is also able to inhibit the activity of plasminogen activator inhibitor-1 (PAI-1), which is involved in cancer progression and metastasis. This compound may be used as an anticancer drug or as a prophylactic agent against cancer. It may also be useful in treating other conditions such as atherosclerosis and restenosis, where PAI-1 plays a significant role. O-Benzyl psilocybin has been found to have anti-inflammatory properties that may be due to its ability to inhibit the production of prostaglandin E2 from arachidonic acid.</p>

<p>4-(Bromomethyl)benzeneboronic acid pinacol ester (BBBA) is a hypochlorous acid derivative with a structural formula of C6H5BrOCH2. It is used as a fluorophore and has been shown to have anticancer activity. 4-Bromomethylbenzeneboronic acid pinacol ester reacts with hydrophobic molecules in the cell membrane, leading to disruption of the membrane and ultimately cell death. This compound can be used as an active oxygen source in biological assays, such as functional assays, because it generates reactive oxygen species and can act as a fluorescence probe for detection of biological samples.</p>

<p>Triethyl borate is an inorganic acid that is used as a catalyst. It has been shown to react with hydrochloric acid and orthoboric acid to form hydrogen boron hydride (H3BO3) and water. It also reacts with hydrogen chloride, forming hydrogen boron chloride, which can be used to prepare the active form of boric acid. This reaction is reversible and the equilibrium can be shifted by adding a base such as sodium hydroxide or ammonia. Triethyl borate is reactive, so it should only be handled in well-ventilated areas. The structural analysis of this compound reveals that it contains two hydroxyl groups that are involved in intramolecular hydrogen bonding, which helps stabilize its structure. Triethyl borate has been shown to have anti-infectious properties, inhibiting the growth of infectious bacteria such as Staphylococcus aureus and Streptococcus pneumoniae.</p>

<p>4-Ethoxyphenylboronic acid is a boron-containing compound that has been shown to have potent antiviral activity. This compound is synthesized from adipose tissue and optical properties of the phenoxazine derivative are studied in order to find an efficient process for solid-phase synthesis. 4-Ethoxyphenylboronic acid has been shown to inhibit triglyceride lipase and fatty acid, which may be an important drug target. It has also been found to have potent antagonistic effects on fatty acids.</p>

<p>O-Benzyl psilocin is a form of the hallucinogenic drug psilocybin. Psilocybin and other related substances are classified as indole alkaloids, which are synthesised by the enzyme tryptophan decarboxylase. O-Benzyl psilocin is synthesised in a two-step reaction that involves catalytic hydrogenation of 4-hydroxyindole to 4-hydroxyphenylacetaldehyde followed by formylation of the latter with formic acid or paraformaldehyde. It was first isolated from sheep's blood serum in 1958 and has been used as an immunogen to produce antisera against cocaine and serotonin. This substance also utilizes a number of endogenous substances for its metabolism, including dopamine, serotonin, noradrenaline, and adrenaline.</p>

<p>Please enquire for more information about 5-Chloropyridine-2-boronicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Vinyloxytrimethylsilane is an organosilicon compound that is used as a polymerization initiator. It reacts with cyclobutanone to form a ruthenium complex, which can be used to coat surfaces and produce polymers. The use of this compound has been shown to increase the reaction yield and decrease the amount of by-products in the polymerization process. Vinyloxytrimethylsilane is biodegradable, making it an environmentally friendly alternative for coating surfaces or producing polymers.</p>

<p>Phenylsilane is a model system for the study of the reaction mechanism of nucleophilic substitution. It is used to investigate the steric interactions between a substrate molecule and an electrophile that are important in determining the rate of reactivity. Phenylsilane has been shown to have antioxidative properties, which may be due to its ability to scavenge reactive oxygen species (ROS), such as hydroxyl radicals, superoxide ions, and hydrogen peroxide. Phenylsilane also has low kinetic energy and can form hydrogen bonds with carbonyl groups and amines. This chemical substance can react with quinoline derivatives, including benzoquinone, which is a toxic by-product of the metabolism of many drugs.</p>

<p>(-)-B-Chlorodiisopinocampheylborane is a carbonyl group that can be used for asymmetric synthesis. It was synthesized from the reaction of chlorodiisopinocampheylborane with butyllithium and allyl bromide, followed by aqueous workup. The enantiomers were separated through thin layer chromatography on silica gel plates with hexane as the eluent. The resolution of racemic latanoprost lactol was achieved in the same manner. (-)-B-Chlorodiisopinocampheylborane is also a diketone that can be prepared from para-chloroacetophenone and sodium hydroxide in ethanol. This diketone undergoes an intramolecular cyclization to produce noradrenaline (norepinephrine) and hydrochloric acid, which can then be converted into dioxolanes or other products.</p>

<p>Pinacol vinylboronate is an anticancer agent that has been shown to inhibit the growth of cancer cells. Pinacol vinylboronate inhibits the activity of cellular targets and generates reactive oxygen species through a hydrogen-bond-mediated mechanism, which eventually leads to cell death. This drug has also been shown to have functional groups that act as pharmacophores for cancer, which may be due to its ability to form hydrogen bonds with the hydroxyl group in DNA.</p>

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<p>1-Hexyl-o-carborane is a human bioassay that has shown carcinogenic activity. It has been observed to cause cancer in humans through its ability to bind to DNA and alter the cell cycle. 1-Hexyl-o-carborane is an organometallic compound that binds to ferrocene and other organometallic compounds, preventing their use as anticancer drugs. 1-Hexyl-o-carborane can be synthesized by reacting hexylmagnesium bromide with ammonium carbonyl chloride in a one pot reaction.</p>

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<p>1-Bromomethyl-o-carborane is a boron compound that has been used as a cross-coupling reagent for the conversion of terminal alkynes to acetonitrile. This reagent is prepared by the reaction of lithium diisopropylamide with dicarbonyl compounds, followed by desilylation and alkylation. The hydroxy group can be substituted with triflates or monosubstituted groups. The nature of these substituents will depend on the desired product and reaction conditions. 1-Bromomethyl-o-carborane has been shown to form hyaluronic acid in yields of up to 98%.</p>

<p>Bis (1,5-Cyclooctadiene) rhodium(I)tetrafluoroborate (BODIPY) is a catalyst that enhances the rate of hydrosilylation reactions. This catalyst has been shown to be effective in the synthesis of aryl chlorides from amines and aldehydes with high enantioselectivity. BODIPY is also immobilized on silica gel to create an active catalyst for asymmetric synthesis. The immobilization process on silica gel is done by reacting BODIPY with ammonium formate and amines. The resulting catalyst can be used for the synthesis of functionalized organic compounds, such as pyrrolidines, tetrahydrofurans, and thiophenes.</p>