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(2R,3R,4S)-2-(tert-butyldiphenylsilanyloxymethyl)-3,4-dihydroxypiperidine-1-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

354153-39-2

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354153-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 354153-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,1,5 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 354153-39:
(8*3)+(7*5)+(6*4)+(5*1)+(4*5)+(3*3)+(2*3)+(1*9)=132
132 % 10 = 2
So 354153-39-2 is a valid CAS Registry Number.

354153-39-2Downstream Products

354153-39-2Relevant academic research and scientific papers

Asymmetric synthesis of the four possible fagomine isomers

Takahata, Hiroki,Banba, Yasunori,Ouchi, Hidekazu,Nemoto, Hideo,Kato, Atsushi,Adachi, Isao

, p. 3603 - 3607 (2003)

The asymmetric synthesis of fagomine and its congeners 1-4 has been achieved by catalytic ring-closing metathesis (RCM). The synthesis involved the construction of the piperidene-type chiral building block 5 followed by dihydroxylation, starting from the D-serine-derived Garner aldehyde 6.

Asymmetric synthesis of fagomine and its congeners

Banba, Yasunori,Abe, Chiemi,Nemoto, Hideo,Kato, Atsushi,Adachi, Isao,Takahata, Hiroki

, p. 817 - 819 (2007/10/03)

The total synthesis of fagomine and its congeners 1-3 has been achieved starting from D-serine-derived Garner aldehyde 5 by catalytic ring-closing metathesis (RCM) for the construction of the piperidine ring followed by dihydroxylation.

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