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(S)-1-((3aS,4R,5R,6aS)-5-Hydroxymethyl-3-oxo-hexahydro-cyclopenta[c]furan-4-carbonyl)-pyrrolidine-2-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

203186-11-2

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203186-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203186-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,1,8 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 203186-11:
(8*2)+(7*0)+(6*3)+(5*1)+(4*8)+(3*6)+(2*1)+(1*1)=92
92 % 10 = 2
So 203186-11-2 is a valid CAS Registry Number.

203186-11-2Relevant academic research and scientific papers

Synthesis of enantiomerically pure, all syn, tetra and pentasubstituted cyclopentanes by the desymmetrisation of endo-norborn-5-ene-2,3-dicarboxylic anhydrides

Jones, Iwan G.,Jones, Wyn,North, Michael

, p. 1478 - 1480 (1997)

Ozonolysis of diastereomerically pure norbornene derivatives incorporating methyl (S)-prolinate provides a route for the synthesis of enantiomerically pure cyclopentanes bearing four or five substituents all orientated syn to one another.

Synthesis of enantio- and diastereomerically pure, tetra- and penta- substituted cyclopentanes by the desymmetrization of endo-norborn-5-ene-2,3- dicarboxylic anhydrides

Hibbs, David E.,Hursthouse, Michael B.,Jones, Iwan G.,Jones, Wyn,Malik, K. M. Abdul,North, Michael

, p. 5413 - 5421 (2007/10/03)

The desymmetrization of endo-norborn-5-ene-2,3-dicarboxylic anhydrides by methyl (S)-prolinate followed by ozonolysis of the resulting carboxylic acids is used to prepare enantio- and diastereomerically pure, tetra- and penta-substituted cyclopentane derivatives in which all of the substituents on the cyclopentane ring are syn to one another. The initial products of this chemistry (2a,b and 18a,b) contain two aldehyde groups, one of which exists as a hemiacetal. This allows subsequent chemistry to be carried out regioselectively at one of the two aldehyde groups. Hence, the sodium borohydride reduction of hemiacetals 2a,b can be controlled to give either a bicyclo[3.2.1] (4) or bicyclo[3.3.0] lactone (5) as the product. The addition of allylindium to hemiacetals 2a,b occurs both regio- and diastereoselectively to give polycyclic acetal 12, the stereochemistry of which is consistent with a chelation controlled addition. It is possible to remove the proline ester based auxiliary from the cyclopentane derivatives by γ-lactone formation under mild reaction conditions.

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