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(S)-6-(4-bromophenyl)-6-(iodomethyl)tetrahydro-2H-pyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1258203-98-3

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1258203-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258203-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,2,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1258203-98:
(9*1)+(8*2)+(7*5)+(6*8)+(5*2)+(4*0)+(3*3)+(2*9)+(1*8)=153
153 % 10 = 3
So 1258203-98-3 is a valid CAS Registry Number.

1258203-98-3Downstream Products

1258203-98-3Relevant academic research and scientific papers

An asymmetric iodolactonization reaction catalyzed by a zinc bis-proline-phenol complex

Filippova, Liudmila,Stenstr?m, Yngve,Hansen, Trond Vidar

supporting information, p. 419 - 422 (2014/01/06)

The intramolecular zinc bis-proline-phenol complex 2a was found to promote enantioselective iodolactonization reactions of both electron-rich and electron-poor 5-aryl-5-hexenoic acids affording δ-iodolactones in good chemical yields with up to 82% enantio

Asymmetric iodolactonization utilizing chiral squaramides

Tungen, Jorn E.,Nolsoe, Jens M. J.,Hansen, Trond V.

, p. 5884 - 5887 (2013/02/23)

Asymmetric iodolactonization of γ- and δ-unsaturated carboxylic acids has been explored in the presence of six different chiral organocatalysts 5-8. The catalyst 6b was found to facilitate the cyclization of 5-arylhex-5-enoic acids 1 to the corresponding

Tertiary aminourea-catalyzed enantioselective iodolactonization

Veitch, Gemma E.,Jacobsen, Eric N.

supporting information; experimental part, p. 7332 - 7335 (2010/12/18)

Binding the anion : A highly enantioselective iodolactonization of 5-hexenoic acids has been achieved using a tertiary aminourea-catalyst (see scheme). The use of catalytic iodine in this process is critical to enhancing both the reactivity and enantioselectivity of the stoichiometric I+ source. The mechanism is proposed to involve binding of an iodonium imidate intermediate by the H-bond donor catalyst.

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