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(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (R,R)-QuinoxP*

CAS
866081-62-1
Catalog Number
ACM866081621
Category
Other Products
Molecular Weight
334.384g/mol
Molecular Formula
C18H28N2P2;

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Specification

Synonyms
AK173366; 866081-62-1; (R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline; (R,R)-QuinoxP; (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline;
IUPAC Name
(R)-tert-butyl-[3-[tert-butyl(methyl)phosphanyl]quinoxalin-2-yl]-methylphosphane;
Canonical SMILES
CC(C)(C)P(C)C1=NC2=CC=CC=C2N=C1P(C)C(C)(C)C;
InChI
InChI=1S/C18H28N2P2/c1-17(2,3)21(7)15-16(22(8)18(4,5)6)20-14-12-10-9-11-13(14)19-15/h9-12H,1-8H3/t21-,22-/m0/s1;
InChI Key
DRZBLHZZDMCPGX-VXKWHMMOSA-N;
Application
Ligand for the rhodium-catalyzed, asymmetric hydrogenation of dehydroamino acid esters and α-enamides.

Ligand for the rhodium-catalyzed, asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds.

Ligand for the rhodium-catalyzed, asymmetric alkylative ring opening reaction

Ligand for the palladium-catalyzed asymmetric allylic alkylation and amination of racemic substrates.

Ligand for the ruthenium-catalyzed asymmetric hydrogenation of ketones.

Ligand for the rhodium-catalyzed, asymmetric hydroacylation of 1,1-disubstituted alkenes with aldehydes.

Ligand for the silver-catalyzed asymmetric nitroso aldol reaction.

Cu-catalyzed enantioconvergent allyllic borylation.

Cu-catalyzed enantioselective cyclopropylation.
Complexity
336
Covalently-Bonded Unit Count
1
Defined Atom Stereocenter Count
2
Exact Mass
334.173g/mol
H-Bond Acceptor
2
Heavy Atom Count
22
Monoisotopic Mass
334.173g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
25.8A^2
Alfa Chemistry

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