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methyl (1R,3S,3aR,6aS)-4,6-dioxo-3-(p-methylphenyl)-5-phenyl-octahydropyrrolo[3,4-c]pyrrole-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1169983-13-4

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1169983-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1169983-13-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,9,9,8 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1169983-13:
(9*1)+(8*1)+(7*6)+(6*9)+(5*9)+(4*8)+(3*3)+(2*1)+(1*3)=204
204 % 10 = 4
So 1169983-13-4 is a valid CAS Registry Number.

1169983-13-4Downstream Products

1169983-13-4Relevant academic research and scientific papers

Development of chiral metal amides as highly reactive catalysts for asymmetric [3 + 2] cycloadditions

Yamashita, Yasuhiro,Yoshimoto, Susumu,Dutton, Mark J.,Kobayashi, Sh?

, p. 1447 - 1452 (2016/08/02)

Highly efficient catalytic asymmetric [3 + 2] cycloadditions using a chiral copper amide are reported. Compared with the chiral CuOTf/Et3 N system, the CuHMDS system showed higher reactivity, and the desired reactions proceeded in high yields a

Metal-free asymmetric 1,3-dipolar cycloaddition of N-arylmaleimides to azomethine ylides catalyzed by chiral tertiary amine thiourea

Bai, Jian-Fei,Wang, Liang-Liang,Peng, Lin,Guo, Yun-Long,Ming, Jun-Nan,Wang, Fei-Ying,Xu, Xiao-Ying,Wang, Li-Xin

, p. 4472 - 4478 (2011/10/01)

The first metal-free asymmetric 1,3-dipolar cycloaddition of N-arylmaleimides to azomethine ylides catalyzed by chiral tertiary amine thiourea to form multiply substituted pyrrolidines in excellent yields (up to 89%) and enantioselectivities (up to 96% ee) is presented. This procedure allows a rapid diversity-oriented synthesis of chiral pyrrolidine derivatives with high optical purity. A series of bifunctional thiourea catalysts were applied for the first time to the highly asymmetric 1,3-dipolar cycloaddition of N-arylmaleimides to azomethine ylides togive the products in excellent yields (up to 89%) and enantioselectivities (up to 96% ee).

Highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides catalyzed by AgOAc/TF-BiphamPhos

Wang, Chun-Jiang,Xue, Zhi-Yong,Liang, Gang,Lu, Zhou

supporting information; experimental part, p. 2905 - 2907 (2009/12/01)

A novel and highly efficient AgOAc/TF-BiphamPhos catalytic system shows excellent reactivity, diastereo-/enantioselectivity and structural scope in asymmetric 1,3-dipolar cycloaddition of azomethine ylides, especially derived from various α-substituted α-amino acids, with N-substituted maleimides and other electron-deficient alkenes.

Axially chiral BINIM and Ni(II)-catalyzed highly enantioselective 1,3-dipolar cycloaddition reactions of azomethine ylides and N-arylmaleimides

Shi, Jing-Wen,Zhao, Mei-Xin,Lei, Zhi-Yu,Shi, Min

, p. 305 - 308 (2008/09/17)

(Chemical Equation Presented) Axially chiral BINIM-Ni(II) complexes are effective catalysts in the asymmetric 1,3-dipolar cycloaddition reactions of azomethine ylides and N-arylmaleimides to give the corresponding adducts in good yields and up to 95% enan

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