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4-cyclohexylbuta-2,3-dien-1-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

869810-22-0

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869810-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869810-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,8,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 869810-22:
(8*8)+(7*6)+(6*9)+(5*8)+(4*1)+(3*0)+(2*2)+(1*2)=210
210 % 10 = 0
So 869810-22-0 is a valid CAS Registry Number.

869810-22-0Downstream Products

869810-22-0Relevant academic research and scientific papers

Enantio- And Diastereodivergent Construction of 1,3-Nonadjacent Stereocenters Bearing Axial and Central Chirality through Synergistic Pd/Cu Catalysis

Huo, Xiaohong,Ma, Shengming,Xiao, Junzhe,Zhang, Jiacheng,Zhang, Wanbin,Zhao, Ling

supporting information, p. 12622 - 12632 (2021/08/31)

In contrast to the widely explored methods for the asymmetric synthesis of molecules bearing a single stereocenter or adjacent stereocenters, the concurrent construction of 1,3-stereogenic centers in an enantio- and diastereoselective manner remains a challenge, especially in acyclic systems. Herein, we report an enantio- and diastereodivergent construction of 1,3-nonadjacent stereocenters bearing allenyl axial and central chirality through synergistic Pd/Cu-catalyzed dynamic kinetic asymmetric allenylation with racemic allenylic esters. The protocol is suitable for a wide range of substrates including the challenging allenylic esters with less sterically bulky substituents and provided chiral allenylic products bearing 1,3-nonadjacent stereocenters with high levels of enantio- and diastereoselectivities (up to >20:1 dr and >99% ee). Furthermore, several representative transformations involving axial-to-central chirality transfer were conducted, affording useful structural motifs containing nonadjacent stereocenters in a diastereodivergent manner.

Dynamic kinetic asymmetric allylic alkylations of allenes

Trost, Barry M.,Fandrick, Daniel R.,Dinh, Diana C.

, p. 14186 - 14187 (2007/10/03)

The dynamic kinetic asymmetric allylic alkylations of racemic allene acetates has been developed with the DACH-phenyl Trost ligand 2 to give general access to allenes with high enantiomeric excess (84-95%) for both malonate and amine nucleophiles. Further

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