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α-Aethoxycarbonyl-<4-methoxy-benzyliden>-triphenylphosphoran, also known as α-ethoxycarbonyl-4-methoxybenzylidene triphenylphosphorane, is a complex organic compound with the chemical formula C29H27O4P. It is a phosphorus-containing reagent used in organic synthesis, particularly in the formation of carbon-carbon bonds through the Wittig reaction. This reaction involves the conversion of aldehydes or ketones into olefins, with the phosphorane acting as a nucleophile. The compound consists of a triphenylphosphine core with an ethoxycarbonyl group (COOEt) and a 4-methoxybenzylidene moiety attached to it. The 4-methoxybenzylidene group is significant as it influences the reactivity and selectivity of the phosphorane in various chemical transformations. α-Aethoxycarbonyl-<4-methoxy-benzyliden>-triphenylphosphoran is a valuable tool in the synthesis of a wide range of organic molecules, including pharmaceuticals and natural products, due to its ability to generate double bonds in a controlled manner.

13125-79-6

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13125-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13125-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13125-79:
(7*1)+(6*3)+(5*1)+(4*2)+(3*5)+(2*7)+(1*9)=76
76 % 10 = 6
So 13125-79-6 is a valid CAS Registry Number.

13125-79-6Downstream Products

13125-79-6Relevant academic research and scientific papers

Construction of Pyrrolo[1,2-a]indoles via Cobalt(III)-Catalyzed Enaminylation of 1-(Pyrimidin-2-yl)-1H-indoles with Ketenimines and Subsequent Base-Promoted Cyclization

Zhou, Xiaorong,Fan, Zili,Zhang, Zhiyin,Lu, Ping,Wang, Yanguang

, p. 4706 - 4709 (2016)

A cobalt(III)-catalyzed cross-coupling reaction of 1-(pyrimidin-2-yl)-1H-indoles with ketenimines is reported. The reaction provided 2-enaminylated indole derivatives in moderate to excellent yields with a broad substrate scope. The prepared 2-enaminylated indoles could be conveniently converted into pyrrolo[1,2-a]indoles, which are an important class of compounds in medicinal chemistry.

Regioselective and Stereoselective Heck-Matsuda Arylations of Trisubstituted Allylic Alkenols and Their Silyl and Methyl Ether Derivatives to Access Two Contiguous Stereogenic Centers: Expanding the Redox-Relay Process and Application in the Total Synthesis of meso-Hexestrol

Frota, Carlise,Polo, Ellen Christine,Esteves, Henrique,Correia, Carlos Roque Duarte

, p. 2198 - 2209 (2018/02/23)

Novel palladium-catalyzed redox-relay Heck arylation reactions of trisubstituted allylic alkenols were developed employing silyl and methyl ethers. The reactions proceeded under mild conditions in moderate to high yields in an excellent anti diastereoselectivity to form α,β-disubstituted methyl ketones containing two contiguous stereocenters. The new redox-relay arylations using silyl and methyl ethers of the starting alkenols demonstrate that the presence of a free hydroxyl group is not a sine qua non condition for an effective redox-relay process as previously thought. Deuterium-labeled alkenols 2-d-10a, 2-d-10b, and 2-d-10c permitted tracking the palladium-hydride reinsertion steps in the conversion of the starting free alcohols, silyl, and methyl ethers into the corresponding methyl ketone 3-d-11a, with >98% deuterium retention. Moreover, the synthetic potential of the method was demonstrated with a straightforward synthesis of the meso-hexestrol in 4 steps, in 41% overall yield from alkenol 10a.

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