-SEGPHOS, >=94%

Code: 692395-100MG D2-231

Application

Takasago Ligands and Complexes for Asymmetric Reactions

Catalytic ligand used for:•Nickel-catalyzed asymmetric A-arylation and heteroarylation of keton...


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Your Price
€48.10 100MG
€59.16 inc. VAT

Application

Takasago Ligands and Complexes for Asymmetric Reactions

Catalytic ligand used for:•Nickel-catalyzed asymmetric A-arylation and heteroarylation of ketones with chloroarenes•Enantioselective synthesis of dihydrobenzofurans and dihydronaphthofurans via olefin isomerization/enantioselective intramolecular Alder-ene reaction of enynes catalyzed by Rh•Preparation of axially chiral biaryl compounds by gold-catalyzed stereoselective intramolecular hydroarylation•Preparation of chiral silylated homoallylic alcohols and diols by asymmetric addition of alcohols and aldehydes to silylbutadienes catalyzed by ruthenium complexes•Preparation of chiral 3-alkyl-substituted indolines by tandem condensation-asymmetric hydrogenation of indoles with aldehydes, catalyzed by Bronsted acids and palladium BINAP complexes•Rhodium-catalyzed asymmetric formal olefination or cycloaddition of 1,3-dicarbonyl compounds with 1,6-diynes or 1,6-enynes

Legal Information

Sold in collaboration with Takasago for research purposes only. JP Registration No. 3148136

SEGPHOS is a registered trademark of Takasago Intl. Corp.

Packaging

100 mg in amber glass bottle

50 mg in glass bottle

assay≥94%
formpowder
InChI keyRZZDRSHFIVOQAF-UHFFFAOYSA-N
InChI1S/C38H28O4P2/c1-5-13-27(14-6-1)43(28-15-7-2-8-16-28)33-23-21-31-37(41-25-39-31)35(33)36-34(24-22-32-38(36)42-26-40-32)44(29-17-9-3-10-18-29)30-19-11-4-12-20-30/h1-24H,25-26H2
mp168-172 °C
optical activity[α]20/D +11°, c = 0.5 in chloroform
Quality Level100
SMILES stringC1Oc2ccc(P(c3ccccc3)c4ccccc4)c(c2O1)-c5c6OCOc6ccc5P(c7ccccc7)c8ccccc8
Cas Number244261-66-3
This product has met the following criteria to qualify for the following awards:



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