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(S)-4-benzyl-3-((2S,3R)-3-hydroxy-2-methyldodecanoyl)oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

460352-58-3

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460352-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 460352-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,3,5 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 460352-58:
(8*4)+(7*6)+(6*0)+(5*3)+(4*5)+(3*2)+(2*5)+(1*8)=133
133 % 10 = 3
So 460352-58-3 is a valid CAS Registry Number.

460352-58-3Relevant academic research and scientific papers

A temporary stereocentre approach for the asymmetric synthesis of chiral cyclopropane-carboxaldehydes

Cheeseman, Matt,Davies, Iwan R.,Axe, Phil,Johnson, Andrew L.,Bull, Steven D.

supporting information; experimental part, p. 3537 - 3548 (2010/01/06)

A novel way of combining chiral auxiliaries and substrate directable reactions is described that employs a three-step sequence of aldol/cyclopropanation/retro-aldol reactions for the asymmetric synthesis of enantiopure cyclopropane-carboxaldehydes. In the first step, reaction of the boron enolate of (S)-N-propionyl-5,5-dimethyl-oxazolidin-2-one with a series of α,β-unsaturated aldehydes affords their corresponding syn-aldol products in high de. In the second step, directed cyclopropanation of the alkene functionalities of these syn-aldols occurs under the stereodirecting effect of their 'temporary'β-hydroxyl stereocentres to give a series of cyclopropyl-aldols in high de. Finally, retro-aldol cleavage of the lithium alkoxide of these cyclopropyl-aldols results in destruction of their temporary β-hydroxy stereocentres to afford the parent chiral auxiliary and chiral cyclopropane-carboxaldehydes in >95% ee. The potential of this methodology has been demonstrated for the asymmetric synthesis of the cyclopropane containing natural product cascarillic acid in good yield.

Synthesis of the Pro-Gly Dipeptide Alkene Isostere Using Olefin Cross-Metathesis

Vasbinder, Melissa M.,Miller, Scott J.

, p. 6260 - 6263 (2007/10/03)

An approach to the synthesis of dipeptide olefin isosteres using intermolecular olefin cross-metathesis is presented. In particular, a synthesis of the Pro-Gly isostere (1) is reported. Conversion of N-BOC-proline into the corresponding vinyl-substituted carbamate provides the N-terminal cross-metathesis partner (2). Methyl 3-butenoate (3) is employed as the C-terminal component. Treatment of the two partners in an optimized molar ratio affords the cross product 1 (83% yield). Three other examples are demonstrated to evaluate the potential of the approach.

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