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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyrrolidine, 1,1',1''-borylidynetris-

C1CCN(C1)B(N1CCCC1)N1CCCC1 Request for Quotation
Chemical Name: Pyrrolidine, 1,1',1''-borylidynetris-
CAS Number: 4426-24-8
Product Number: AG00DLLJ(AGN-PC-0L5PLX)
Synonyms:
MDL No:
Molecular Formula: C12H24BN3
Molecular Weight: 221.15006

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Chemical Structure


1,1′,1′′-Borylidynetris[pyrrolidine] is a versatile compound that finds wide application in chemical synthesis. One of its key uses lies in its ability to serve as a chiral ligand in metal-catalyzed reactions. This compound can efficiently complex with various transition metals, such as palladium and rhodium, to catalyze a range of asymmetric transformations. The resulting metal-ligand complexes exhibit high stability and reactivity, making them valuable tools in enantioselective synthesis. Additionally, 1,1′,1′′-Borylidynetris[pyrrolidine] can participate in organic reactions as a versatile organoboron reagent, enabling the selective formation of carbon-carbon and carbon-heteroatom bonds. Its unique chemical properties make it a valuable component in the toolbox of synthetic chemists seeking to efficiently access complex molecular structures with high levels of stereocontrol.