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700665-100MG
Sigma-Aldrich
(11bR)-2,6-Di-9-phenanthrenyl-4-hydroxy-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-oxide
Price: $484.90List Price: $538.78Application Catalyst for: Asymmetric hydrogenation cascade Enantioselective Friedel-Crafts reaction Asymmetric hydrogenation of 2-substituted quinolines Chiral Broensted acid catalyzed enantioselective a-aminoxylation of ene carbamates Preparation -
448427-1G
Sigma-Aldrich
(4R)-2-Hydroxy-5,5-dimethyl-4-phenyl-1,3,2-dioxaphosphorinan 2-oxide
Price: $315.83List Price: $350.92Application (4 R )-2-Hydroxy-5,5-dimethyl-4-phenyl-1,3,2-dioxaphosphorinan 2-oxide can be used: As a reactant in the phosphoalkoxylation of aromatic enones. As a chiral resolving agent in the resolution of amino acids, amines, and amino alcohols. -
543039-1GApplication Reactant for: Proline-catalyzed Diels Alder reaction Stereodivergent synthesis of carbahexofuranoses employing a Wittig olefination-Claisen rearrangement protocol Wittig reactions Crotylation reactions Asymmetric synthesis of
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1031151000EMPLURA ® is our low-cost alternative to high-purity qualities. With EMPLURA we offer a range of solvents for a plurality of basic applications in non-regulated industries and for less demanding applications, preparative laboratory work and
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1031152500EMPLURA ® is our low-cost alternative to high-purity qualities. With EMPLURA we offer a range of solvents for a plurality of basic applications in non-regulated industries and for less demanding applications, preparative laboratory work and
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283061-5GThe reactivity of molybdenum pentachloride with1,3-dioxane has been investigated at room temperature in a non-coordinating solvent (dichloromethane) . Application 1,3-Dioxane has been employed as solvent in the synthesis of 8- and 9-membered
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296309-100MLApplication 1,4-Dioxane may undergo nickel-catalyzed oxidative arylation with arylboronic acids to form α-arylated ethers. It may be used as a solvent to synthesize: (Chloromethyl)dimethylphenylsilane from chloro(chloromethyl)dimethylsilane
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296309-12X100MLApplication 1,4-Dioxane may undergo nickel-catalyzed oxidative arylation with arylboronic acids to form α-arylated ethers. It may be used as a solvent to synthesize: (Chloromethyl)dimethylphenylsilane from chloro(chloromethyl)dimethylsilane
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296309-18LApplication 1,4-Dioxane may undergo nickel-catalyzed oxidative arylation with arylboronic acids to form α-arylated ethers. It may be used as a solvent to synthesize: (Chloromethyl)dimethylphenylsilane from chloro(chloromethyl)dimethylsilane
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296309-1LApplication 1,4-Dioxane may undergo nickel-catalyzed oxidative arylation with arylboronic acids to form α-arylated ethers. It may be used as a solvent to synthesize: (Chloromethyl)dimethylphenylsilane from chloro(chloromethyl)dimethylsilane
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296309-2LApplication 1,4-Dioxane may undergo nickel-catalyzed oxidative arylation with arylboronic acids to form α-arylated ethers. It may be used as a solvent to synthesize: (Chloromethyl)dimethylphenylsilane from chloro(chloromethyl)dimethylsilane
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34857-100ML1,4-Dioxane is widely used as a solvent for various organic compounds in industry. It is a non-biodegradable contaminant found in industrial effluents.