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(R)-(-)-3-(dimethylphenylsilyl)-3-phenyl-1-propene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

945684-74-2

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945684-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 945684-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,6,8 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 945684-74:
(8*9)+(7*4)+(6*5)+(5*6)+(4*8)+(3*4)+(2*7)+(1*4)=222
222 % 10 = 2
So 945684-74-2 is a valid CAS Registry Number.

945684-74-2Downstream Products

945684-74-2Relevant academic research and scientific papers

Asymmetric catalysis with silicon-based cuprates: Enantio- and regioselective allylic substitution of linear precursors

Hensel, Alexander,Oestreich, Martin

, p. 9062 - 9065 (2015/06/16)

An enantio- and regioselective allylic silylation of linear allylic phosphates that makes use of catalytically generated cuprate-type silicon nucleophiles is reported. The method relies on soft bis(triorganosilyl) zincs as silicon pronucleophiles that are prepared in situ from the corresponding hard lithium reagents by transmetalation with ZnCl2. With a preformed chiral N-heterocyclic carbene-copper(I) complex as catalyst, exceedingly high enantiomeric excesses are achieved. The new method is superior to existing ones using a silicon-boron reagent as the source of the silicon nucleophile. Zinc about it: Cuprates catalytically generated from bis(triorganosilyl)zinc compounds and a preformed chiral N-heterocyclic carbene-copper(I) complex allow for the highly enantio- and regioselective allylic silylation of various allylic phosphates. The method is broadly applicable with regard to the silicon pronucleophile and the allylic acceptor. It is the first example of asymmetric catalysis with a silicon-based cuprate.

Enantioselective synthesis of α-tri- and α-tetrasubstituted allylsilanes by copper-catalyzed asymmetric allylic substitution of allyl phosphates with silylboronates

Takeda, Momotaro,Shintani, Ryo,Hayashi, Tamio

, p. 5007 - 5017 (2013/07/11)

A copper/N-heterocyclic carbene-catalyzed asymmetric allylic substitution of allyl phosphates with a silylboronate has been developed to give highly enantioenriched allylsilanes. High regioselectivity has been achieved by employing NaOH as the base, and this catalyst system is effective for both γ-mono- and disubstituted allyl phosphates.

Asymmetric synthesis of α-chiral allylic silanes by enantioconvergent γ-selective copper(I)-catalyzed Allylic Silylation

Delvos, Lukas B.,Vyas, Devendra J.,Oestreich, Martin

, p. 4650 - 4653 (2013/06/05)

Gamma way: Regio- and enantioselective allylic substitution with a silicon nucleophile generated by copper(I)-catalyzed Si-B bond activation provides direct access to α-chiral allylic silanes from linear acceptors. The enantioconvergent catalysis employing McQuade's six-membered N-heterocyclic-carbene-copper(I) catalyst is applicable to aryl- and alkyl-substituted allylic phosphates (see scheme). Copyright

Enantioselective synthesis of allylsilanes bearing tertiary and quaternary si-substituted carbons through Cu-catalyzed allylic alkylations with alkylzinc and arylzinc reagents

Kacprzynski, Monica A.,May, Tricia L.,Kazane, Stephanie A.,Hoveyda, Amir H.

, p. 4554 - 4558 (2008/09/17)

All sorts of allylsilanes including, for the first time, those that contain a Si-bonded quaternary carbon, were synthesized through efficient and highly enantioselective Cu-catalyzed asymmetric allylic alkylations. Reactions may involve dialkyl- as well as diarylzinc reagents and are promoted by various chiral N-heterocyclic carbene complexes.

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