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8,8-diphenyl-6,10-dioxa-spiro[4.5]dec-3-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

351194-45-1

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351194-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 351194-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,1,9 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 351194-45:
(8*3)+(7*5)+(6*1)+(5*1)+(4*9)+(3*4)+(2*4)+(1*5)=131
131 % 10 = 1
So 351194-45-1 is a valid CAS Registry Number.

351194-45-1Relevant academic research and scientific papers

Asymmetric Conjugate Addition of Alkylzirconocenes to Cyclopent-4-ene-1,3-dione Monoacetals

Rideau, Emeline,M?sing, Florian,Fletcher, Stephen P.

, p. 2217 - 2222 (2015)

Copper-catalyzed asymmetric conjugate additions are powerful reactions that allow the formation of single-enantiomer building blocks in a few steps. However, highly enantioselective conjugate addition to five-membered-ring substrates is more challenging a

Catalytic enantioselective synthesis of (-)-prostaglandin E1 methyl ester based on a tandem 1,4-addition-aldol reaction

Arnold, Leggy A.,Naasz, Robert,Minnaard, Adriaan J.,Feringa, Ben L.

, p. 7244 - 7254 (2007/10/03)

Catalytic enantioselective 1,4-additions and tandem 1,4-addition-aldol reactions of dialkylzinc reagents to cyclopentene-3,5-dione monoacetals in the presence of an in situ generated Cu(OTf)2/chiral phosphoramidite catalyst result in highly functionalized cyclopentane building blocks with ee's up to 97%. A new synthesis of cyclopentene-3,5-dione monoacetals is presented as well as its use in a tandem 1,4-addition-aldol protocol for the catalytic asymmetric total synthesis of (-)-PGE1 methyl ester. This synthesis represents a new approach to this class of natural products. By using only 3 mol % of an enantiomerically pure catalyst in the key step, the absolute configurations at three stereocenters of the basic structure of the PGE1 are established at once.

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