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830335-26-7

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830335-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 830335-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,0,3,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 830335-26:
(8*8)+(7*3)+(6*0)+(5*3)+(4*3)+(3*5)+(2*2)+(1*6)=137
137 % 10 = 7
So 830335-26-7 is a valid CAS Registry Number.

830335-26-7Downstream Products

830335-26-7Relevant academic research and scientific papers

Cyclizations of aminyl radicals generated from substoichiometric stannane

Zhai, Huimin,Wickenden, Jason G.,Sammis, Glenn M.

supporting information; experimental part, p. 3035 - 3038 (2011/02/24)

Substoichiometric amounts of tributyltin hydride were utilized in nitrogen-centered radical cyclizations onto silyl enol ethers for the formation of substituted cyclic imines

Stereoselective synthesis of substituted N-heterocycles via sequential cross metathesis-reductive cyclization

Gebauer, Julian,Dewi, Purnama,Blechert, Siegfried

, p. 43 - 46 (2007/10/03)

A diastereoselective synthesis of substituted piperidine and pyrrolidine derivatives is presented, employing a highly selective cross metathesis (CM) reaction followed by a domino reduction-cyclization process. A diastereoselective synthesis of substituted mono- and bicyclic-piperidine and pyrrolidine derivatives is presented, employing a highly selective cross metathesis (CM) reaction followed by a domino reduction-cyclization process.

New Diastereoselective Route to 2-Substituted cis-(2S,5S)- and trans-(2S,5R)-5-Alkylpyrrolidines as Indolizidine and Pyrrolizidine Scaffolds

Mota, Antonio J.,Chiaroni, Angele,Langlois, Nicole

, p. 4187 - 4198 (2007/10/03)

A new and short stereoselective route to the synthesis of enantiopure cis-2,5-disubstituted pyrrolidines as indolizidine or pyrrolizidine scaffolds has been developed. The method, which uses (S)-pyroglutamic acid as a chiral starting material, is based on the ring opening of N-protected 7-lactams by alkyl phenyl sulfone carbanions, followed by desulfonylation and reductive amination of alkyl 7-amino ketones. The diastereoselectivity depends on the substitution of the starting γ-lactams, and on the alkyl group of the phenyl sulfone. Total cis diastereoselectivity was observed in the formation of tert-butyl 5-alkylprolinates. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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