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2-Phenyl-1-oxaspiro<2.5>octan-4-on is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13243-58-8

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13243-58-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13243-58-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,4 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13243-58:
(7*1)+(6*3)+(5*2)+(4*4)+(3*3)+(2*5)+(1*8)=78
78 % 10 = 8
So 13243-58-8 is a valid CAS Registry Number.

13243-58-8Relevant academic research and scientific papers

Epoxidation of Alkenes with Molecular Oxygen as the Oxidant in the Presence of Nano-Al 2O 3

Zhou, Xuan,Wang, Qiong,Xiong, Wenfang,Wang, Lu,Ye, Rongkai,Xiang, Ge,Qi, Chaorong,Hu, Jianqiang

supporting information, p. 1789 - 1794 (2020/09/18)

The nano-Al 2O 3-promoted epoxidation of alkenes with molecular oxygen as the oxidant has been developed, providing an efficient route to a variety of epoxides in moderate to excellent yields. The environmentally friendly and efficient nano-Al 2O 3catalyst could be easily recovered and reused five times without significant loss of activity.

Stereodivergent Access to Enantioenriched Epoxy Alcohols with Three Stereogenic Centers via Ruthenium-Catalyzed Transfer Hydrogenation

Zhao, Zhifei,Bagdi, Prasanta Ray,Yang, Shuang,Liu, Jinggong,Xu, Weici,Fang, Xinqiang

supporting information, p. 5491 - 5494 (2019/08/01)

The resolution technique of stereodivergent reaction on racemic mixtures (stereodivergent RRM) was employed for the first time in ruthenium complex catalyzed transfer hydrogenation of racemic epoxy ketones, providing a new and very simple method that allows access to enantioenriched epoxy alcohols with three stereogenic centers in a one-step fashion. The protocol features simple reaction conditions, practical operation, ability to scale up, and broad group tolerance.

An efficient Darzens reaction promoted by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)

Luo, Juan,Hu, Lanfang,Zhang, Minghao,Tang

supporting information, p. 1949 - 1951 (2019/07/03)

An efficient DBU promoted Darzens reaction utilising α-haloketones containing an enolizable α′-hydrogen is reported. This method diastereoselectively afforded the corresponding α,β-epoxy ketones good to excellent yields in an one-pot reaction without using any transition metals or additives. Furthermore, haloketones without an α′-hydrogen are also applicable in this reaction.

Preparation method and applications of parthenolide analogues

-

Paragraph 0044; 0045; 0046; 0047; 0048; 0061; 0062, (2016/10/10)

The invention relates to a preparation method and applications of parthenolide analogues, and belongs to the field of organic synthesis. On the basis of reserving the main active group alpha-methylene-gamma-lactone and epoxide structure of parthenolide, series of compounds are designed by changing its framework, and its in-vitro antitumor activity is tested. Series of parthenolide analogues having biological activity are synthesized by a simple method, wherein two compounds are nontoxic to normal cells.

Highly chemo- and regioselective rearrangement of α,β-epoxy ketones to 1,3-dicarbonyl compounds in 5 mol dm-3 lithium perchlorate-diethyl ether medium

Sankararaman,Ncsakumar

, p. 3173 - 3175 (2007/10/03)

Epoxides from α,β-unsaturated ketones undergo highly chemo- and regioselective rearrangement to 1,3-dicarbonyl compounds in 5 mol dm-3 lithium perchlorate-diethyl ether medium by a 1,2-migration of the carbonyl group at ambient conditions. The Royal Society of Chemistry 1999.

A Novel Darzens-Type Reaction Promoted by Tributylstannylcarbamate

Shibata, Ikuya,Yamasaki, Hayahide,Baba, Akio,Matsuda, Haruo

, p. 6909 - 6914 (2007/10/02)

Stannylcarbamate 1 proved to be a selective agent for generating organotin(IV) enolates from α-halo ketones.Thus, a Darzens reaction was achieved under mild and neutral conditions.The reaction took place without any side reactions and even with aliphatic α-halo ketones bearing enolizable α'-hydrogens.Various types of α,β-epoxy ketones and esters were obtained in this one-pot reaction.The stereoselectivity of the reaction was influenced by changing the halogen substituent of the α-halo ketones and by additives.Moreover, the present method could be appliedto γ- and δ-halo ketones as enolate precursors, and five- and six-membered cyclic compounds were obtained.

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