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Postion:Product Catalog >Chemical Reagents>Organic reagents>Phosphine ligand>di(naphthalen-1-yl)phosphine oxide
di(naphthalen-1-yl)phosphine oxide
  • di(naphthalen-1-yl)phosphine oxide
  • di(naphthalen-1-yl)phosphine oxide

di(naphthalen-1-yl)phosphine oxide

Price $1
Package 1KG
Min. Order: 1G
Supply Ability: 1MT
Update Time: 2019-07-06

Product Details

Product Name: di(naphthalen-1-yl)phosphine oxide CAS No.: 162291-02-3
Min. Order: 1G Purity: 98%
Supply Ability: 1MT Release date: 2019/07/06

AD68

(S)-(R)-JOSIPHOS Basic information
Reactions
Product Name: (S)-(R)-JOSIPHOS
Synonyms: (S)-(+)-1-[(R)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct,97% (S)-(R)-JOSIPHOS;(S)-(+)-1-[(R)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine ethanol adduct (S)-(R)-JOSIPHOS;(S)-1-[(RP)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine >=97%;(S)-(+)-1-[(R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;(S)-1-[(1R)-2-(DIPHENYLPHOSPHINO)FERROCENYL]ETHYLDICYCLOHEXYLPHOSPHINE;(S,S)-1-[1-(DICYCLOHEXYLPHOSPHINO)ETHYL]-2-(DIPHENYLPHOSPHINO)FERROCENE;(S)-(R)-JOSIPHOS;JOSIPHOS SL-J001-2
CAS: 162291-02-3
MF: C36H44FeP2 10*
MW: 594.53
EINECS:  
Product Categories: Chiral Phosphine;Ferrocene Series;Josiphos Series;organophosphine ligand
Mol File: 162291-02-3.mol
Article illustration
 
(S)-(R)-JOSIPHOS Chemical Properties
alpha  +360° (c 0.5, CHCl3)
form  Powder
color  orange
Stability: store cold
 
Safety Information
Risk Statements  36/37/38
Safety Statements  26-36/37/39
WGK Germany  3
10
 
(S)-(R)-JOSIPHOS Usage And Synthesis
Reactions
  1. Ferrocenylphosphine ligands of the type cpFecp(PR2)(*CH(CH3)PR'2) are a class of asymmetric ligands developed at Solvias in Basel, Switzerland. Ligands of this type are currently used industrially in the stereoselective synthesis of commercial products. A unique feature of these bidentate ligands is the presence of a fixed phosphine moiety and a stereogenic,functionalized side chain, which can be easily modified to accommodate electronic and steric requirements. Based on a versatile synthetic procedure starting with optically active ferrocenes of the type cpFecp(PR2)(*CH(CH3)X) [X = OAc or NR2], a variety of donor atoms can be introduced into the side chain.4 These ferrocene based phosphine ligands have wide application in the stereoselective hydrogenation of substituted acetamidoacrylates, enol acetates, β-ketoesters and simple alkenes.
  2. Pd-catalyzed, enantioselective, intramolecular α-substituted cyclic ketones: facile synthesis of functionalized chiral spirobicycles.
  3. Asymmetric boron conjugate addition of α,β-unsaturated carbonyl compounds catalyzed by
  4. CuOTf/Josiphos under non-alkaline conditions.
  5. Chiral amides via copper-catalyzed enantioselective conjugate addition.
  6. Ruthenium-catalyzed enantioselective synthesis of β-amino alcohols from 1,2-diols by “borrowing hydrogen”.
  7. Cobalt-catalyzed asymmetric addition of silylacetylenes to 1,1-disubstituted allenes.
Article illustration
Chemical Properties Dark orange powder
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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