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methyl 2-acetamido-2-phenylpent-4-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

848829-40-3

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848829-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848829-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,8,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 848829-40:
(8*8)+(7*4)+(6*8)+(5*8)+(4*2)+(3*9)+(2*4)+(1*0)=223
223 % 10 = 3
So 848829-40-3 is a valid CAS Registry Number.

848829-40-3Downstream Products

848829-40-3Relevant academic research and scientific papers

Chemo- and Enantioselective Pd/B Hybrid Catalysis for the Construction of Acyclic Quaternary Carbons: Migratory Allylation of O-Allyl Esters to α- C-Allyl Carboxylic Acids

Fujita, Taiki,Yamamoto, Tomohiro,Morita, Yuya,Chen, Hongyu,Shimizu, Yohei,Kanai, Motomu

supporting information, p. 5899 - 5903 (2018/05/14)

We describe herein the asymmetric synthesis of α-allyl carboxylic acids containing an α-quaternary stereocenter by a chiral hybrid catalyst system comprising palladium and boron complexes. The reaction proceeded through palladium-catalyzed ionization of α,α-disubstituted O-allyl esters for the generation of chiral π-allyl palladium complex as an electrophile, boron-catalyzed enolization of the carboxylate part for the generation of chiral α,α-disubstituted carboxylic acid-derived enolates as a nucleophile, and enantioselective coupling between the thus-generated nucleophile and electrophile. Proper combinations of chiral ligands for the boron and palladium catalysts were crucial. The reaction proceeded chemoselectively at the α-position of the carboxylic acid group.

Stereoselective synthesis of 4-hydroxy-2-phenylproline framework

Maeda, Kenji,Miller, Ross A.,Szumigala Jr., Ronald H.,Shafiee, Ali,Karady, Sandor,Armstrong III, Joseph D.

, p. 1545 - 1549 (2007/10/03)

Highly diastereoselective (>20:1) bromo-lactonization of N-sulfonyl-2-allyl-2-phenylglycine methyl ester (11) was observed. Successive treatment of the chiral lactone with MeONa gave the desired (2S,4R)-4-hydroxy-2- phenylproline derivative in high yield without erosion of the diastereoselectivity. The starting chiral non-racemic compound (5) was prepared from the racemic 2-phenylglycine using a classical kinetic resolution (crystallization), an asymmetric phase transfer alkylation, and an enzyme-catalyzed kinetic resolution.

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