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(-)-(R,S,R)-1-hydroxy-2,3-epoxy-1,3-diphenylpropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

229018-00-2

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229018-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 229018-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,0,1 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 229018-00:
(8*2)+(7*2)+(6*9)+(5*0)+(4*1)+(3*8)+(2*0)+(1*0)=112
112 % 10 = 2
So 229018-00-2 is a valid CAS Registry Number.

229018-00-2Relevant academic research and scientific papers

Enantioselective one-pot catalytic synthesis of 4,5-epoxy-3-alkanols and 1-Phenyl-2,3-epoxy-1-alkanols from α,β-unsaturated aldehydes

Infante, Rebeca,Hernandez, Yulan,Nieto, Javier,Andres, Celia

supporting information, p. 4863 - 4869 (2013/08/23)

Conformationally restricted perhydrobenzoxazines have been demonstrated to be good chiral ligands for one-pot asymmetric ethylation/epoxidation, and the unprecedented arylation/epoxidation of trisubstituted α,β-unsaturated aldehydes. The scope of the reaction has been studied and a wide set of substrates with allylic strain of different nature has been explored, obtaining good or total diastereoselectivities in all cases. The enantiocontrol was good or high for the ethylation/epoxidation reaction, whereas it remained at moderate or good levels for the arylation/epoxidation. The reaction is general for trisubstituted enals, and alkylic and aromatic substituents are tolerated at both the α- and β-position of the unsaturated aldehyde; however, disubstituted enals remain challenging substrates. When the one-pot and two-pot protocols were compared, no significant differences concerning the stereocontrol were found, so the advantages of the one-pot procedure are clear. Copyright

Asymmetric allylic substitution reaction with nitrogen and oxygen nucleophiles using monodentate chiral phosphine, 9-PBN

Hamada, Yasumasa,Seto, Noriko,Takayanagi, Yoshie,Nakano, Takeshi,Hara, Osamu

, p. 7791 - 7794 (2007/10/03)

Asymmetric allylic substitution reactions between 1,3-diphenyl-2-propenyl acetate and various hetero nucleophiles were efficiently carried out using the catalysts derived from the monodentate phosphine ligands, (1R, 2S, 5R, 6S)-2,6-dimethyl-9-phenyl-9-phosphabicyclo[3.3.1] nonane and its enantiomer ((-)- and (+)-9-PBNs), and palladium (0).

PaaSicats: Powerful catalysts for asymmetric epoxidation of enones. Novel syntheses of α-arylpropanoic acids including (S)-fenoprofen

Carde, Lydia,Davies, Huw,Geller, Thomas P.,Roberts, Stanley M.

, p. 5421 - 5424 (2007/10/03)

Application of the recently developed silica-adsorbed polyleucine catalysts to the enantioselective epoxidation of two enones is reported. Treatment of these epoxides with trimethylaluminium in moist dichloromethane generates the α-hydroxy-β-methylketones, with inversion of configuration. Diastereoselective reduction of the ketone moiety followed by oxidative cleavage generates α-arylpropanoic acids.

Synthesis of novel C2-symmetric ligands based on (R,R)- and (S,S)- diphenyl-1,3-propanediol

Roos, Gregory H. P.,Donovan, A. Richard

, p. 991 - 1000 (2007/10/03)

A range of novel C2-symmetric dioxygen and dinitrogen ligands can readily be obtained through the interconversion of the parent 1,3-diphenyl- 1,3-propanediol enantiomers which are, in turn, accessed in good yields via a Sharpless asymmetric epoxidative resolution.

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