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Cyclopentanecarboxylic acid, 2-oxo-1-[(2E)-3-phenyl-2-propenyl]-, methyl ester, (1S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

685139-89-3

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685139-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 685139-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,1,3 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 685139-89:
(8*6)+(7*8)+(6*5)+(5*1)+(4*3)+(3*9)+(2*8)+(1*9)=203
203 % 10 = 3
So 685139-89-3 is a valid CAS Registry Number.

685139-89-3Downstream Products

685139-89-3Relevant academic research and scientific papers

Development of a new class of chiral phosphorus ligands: P-chirogenic diaminophosphine oxides. A unique source of enantioselection in Pd-catalyzed asymmetric construction of quaternary carbons

Nemoto, Tetsuhiro,Masuda, Takamasa,Matsumoto, Takayoshi,Hamada, Yasumasa

, p. 7172 - 7178 (2005)

We have recently developed a new class of chiral phosphorus ligands: P-chirogenic diaminophosphine oxides. These pentavalent phosphorus compounds have been successfully applied to Pd-catalyzed asymmetric construction of tertiary and quaternary carbons. The actual ligand structure was the trivalent phosphorus species 17, which was generated in situ by BSA-induced P(V) to P(III) transformation of 6, the preligand. Detailed mechanistic studies, including asymmetric amplification and initial rate kinetics, revealed that complex 18 [Pd-17 (1:2) complex] was the active catalyst. The important function of the nitrogen atom on the sidearm in the ligands was also clarified. The source of enantioselection in the construction of asymmetric quaternary carbons was the secondary ligand substrate interaction mediated by N-Zn coordination.

P-Chirogenic Diaminophosphine Oxide: A New Class of Chiral Phosphorus Ligands for Asymmetric Catalysis

Nemoto, Tetsuhiro,Matsumoto, Takayoshi,Masuda, Takamasa,Hitomi, Tsukasa,Hatano, Keiichiro,Hamada, Yasumasa

, p. 3690 - 3691 (2007/10/03)

We successfully synthesized a novel P-chirogenic diaminophosphine oxide 4, which was applied to catalytic enantioselective construction of quaternary carbon centers using Pd-catalyzed asymmetric allylic substitution with various β-keto esters (up to 99% yield, 94% ee). Preliminary mechanistic studies indicated that two molecules of 8 coordinate to the Pd metal in a monodentate fashion, resulting in the formation of Pd complex 9 (Pd:8 = 1:2), which functions as the active species. Copyright

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