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(R)-3-[N-(tert-butyloxycarbonyl)-N-(2-carbomethoxyethyl)]amino-4-phenylbutyric acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

226213-90-7

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226213-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226213-90-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,2,1 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 226213-90:
(8*2)+(7*2)+(6*6)+(5*2)+(4*1)+(3*3)+(2*9)+(1*0)=107
107 % 10 = 7
So 226213-90-7 is a valid CAS Registry Number.

226213-90-7Downstream Products

226213-90-7Relevant academic research and scientific papers

Diastereoselective synthesis of 2,4,5-trisubstituted piperidines from enantiopure β-amino esters

Ma, Dawei,Sun, Haiying

, p. 3609 - 3612 (1999)

Reaction of (R)-β-amino esters with methyl acrylate followed by Dieckmann condensation and enol silylation afforded the enol ethers 5, which were hydrogenated with catalysis by Raney-Ni to provide 2,4,5-trisubstituted piperidines with high diastereoselectivity.

General Route to 2,4,5-Trisubstituted Piperidines from Enantiopure ss-Amino Esters. Total Synthesis of Pseudodistomin B Triacetate and Pseudodistomin F

Ma, Dawei,Sun, Haiying

, p. 6009 - 6016 (2007/10/03)

The Michael addition reaction of enantiopure ss-amino esters with methyl acrylate followed by Dieckmann condensation and enol silylation affords the enol ethers 6, which are hydrogenated with catalysis by Raney-Ni at 80 atm and 80°C to provide 2,4,5-trisubstituted piperidines with high diastereoselectivity. In this case Ni-H attacks the C-C double bond from the direction of the 2-alkyl group to provide the products in which 2,4,5-trisubstrited groups are all cis to each other. While hydrogenation of enol ether 13 without a N-Boc protecting group gives the product 15 in which the 4-hydroxy group and 5-ester moiety are trans to the 2-alkyl group. By using the diastereoselective hydrogenation products 9d and 9e as key intermediates, pseudodistomin B triacetate and pseudodistomin F are synthesized. The key steps for these transformations include Curtius rearrangement and Julia olefination.

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