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((E)-4-Phenyl-but-3-enyl)-phosphonic acid diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71071-58-4

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71071-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71071-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,7 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71071-58:
(7*7)+(6*1)+(5*0)+(4*7)+(3*1)+(2*5)+(1*8)=104
104 % 10 = 4
So 71071-58-4 is a valid CAS Registry Number.

71071-58-4Downstream Products

71071-58-4Relevant academic research and scientific papers

8π Electrocyclic Reaction of Phosphonate Derivatives: Access to Seven-Membered Cross-Conjugated Cyclic Trienes

Saito, Hiroki,Kato, Ranmaru,Ikeuchi, Kazutada,Suzuki, Takahiro,Tanino, Keiji

supporting information, p. 9606 - 9610 (2021/12/17)

An anionic 8π electrocyclic reaction of 4-(diethoxyphosphoryl)-1,3,6-heptatriene derivatives was developed. Under the influence of a base, the substrate underwent deprotonation at the C5 position followed by the 8π electrocyclization of the resulting hept

Remote Functionalization of α,β-Unsaturated Carbonyls by Multimetallic Sequential Catalysis

Romano, Ciro,Fiorito, Daniele,Mazet, Clément

, p. 16983 - 16990 (2019/10/28)

The remote functionalization of α,β-unsaturated carbonyls by an array of multimetallic sequential catalytic systems is described. The reactions are triggered by hydrometalation using [Pd-H] or [Ru-H] isomerization catalysts and driven by the formation of thermodynamically more stable 1,2-vinyl arenes. The Pd-catalyzed deconjugative isomerization was combined with a Cu-catalyzed β-borylation of the transiently generated styrenyl derivatives to deliver a range of products that would not be accessible with the use of a single catalyst. [Pd/Cu] catalytic systems were also identified for the highly enantioselective α-hydroboration and α-hydroamination of the styrenyl intermediates. Difunctionalization simultaneously at the benzylic and homobenzylic positions was achieved by combining the isomerization process with Sharpless asymmetric dihydroxylation (SAD) using [Pd/Os] or [Ru/Os] couples. Starting from a simple α,β-unsaturated ester, an isomerization/dihydroxylation/lactonization sequence gave access to a naturally occurring γ-butyrolactone in good yield, with excellent diastereo- and enantioselectivity.

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