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3-((E)-2-Benzenesulfonyl-vinyloxy)-selenobutyric acid Se-phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

199862-40-3

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199862-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199862-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,8,6 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 199862-40:
(8*1)+(7*9)+(6*9)+(5*8)+(4*6)+(3*2)+(2*4)+(1*0)=203
203 % 10 = 3
So 199862-40-3 is a valid CAS Registry Number.

199862-40-3Downstream Products

199862-40-3Relevant academic research and scientific papers

Stereoselective synthesis of cyclic ethers using vinylogous sulfonates as radical acceptors: Effect of E/Z geometry and temperature on diastereoselectivity

Evans, P Andrew,Manangan, Thara

, p. 4523 - 4528 (2007/10/03)

Treatment of the E-vinylogous sulfonates 1a-g with tris(trimethylsilyl)silane and triethylborane, in the presence of air, furnished the cyclic ethers 2/3a-g with good to excellent diastereoselectivity favoring the cis-isomer 2. This study demonstrated the level of stereocontrol in a 6-exo radical cyclization and may be attributed to the type of radical intermediate. Hence, the modest selectivity obtained for the cyclization of 1e may be a function of the acyl radical geometry (sp2) and high inversion barrier (29 kcal/mol) as compared to the alkyl (1 kcal/mol) and vinyl (2.9 kcal/mol) radicals. This is consistent with the acyl radical cyclization having an earlier transition state than the corresponding alkyl and vinyl radicals. The modest diastereoselectivity can be improved dramatically using the Z-vinylogous sulfonate (≥34:1; R = Ph) to promote kinetic trapping of the s-trans rotamer I and III, respectively (Figure 1). The 5-exo alkyl radical cyclization reaction under nonreductive Keck-allylation conditions was also examined, in which 8 was formed in 91% overall yield. This transformation provides a convenient method for in situ homologation and should be applicable to target directed synthesis.

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