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35590-18-2

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35590-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35590-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,9 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35590-18:
(7*3)+(6*5)+(5*5)+(4*9)+(3*0)+(2*1)+(1*8)=122
122 % 10 = 2
So 35590-18-2 is a valid CAS Registry Number.

35590-18-2Relevant academic research and scientific papers

Synthesis of Highly Fused Pyrano[2,3- b]pyridines via Rh(III)-Catalyzed C-H Activation and Intramolecular Cascade Annulation under Room Temperature

Han, Xu,Gao, Feng,Li, Chunpu,Fang, Daqing,Xie, Xiong,Zhou, Yu,Liu, Hong

supporting information, p. 6281 - 6294 (2020/03/05)

A facile access to the polycyclic-fused pyrano[2,3-b]pyridines has been established under room temperature via Rh(III)-catalyzed C-H bond activation and intramolecular cascade annulation. This strategy features high efficiency, unique versatility, and gen

New method for preparing isopropyl ester benzimidate

-

Paragraph 0014-0021, (2019/04/26)

The invention relates to the technical field of fine chemicals, and discloses a new method for preparing isopropyl ester benzimidate. The specific steps comprise: carrying out a stirring reaction on benzamide, isopropyl bromide, cobalt perchlorate hexahyd

Flow rhodaelectro-catalyzed alkyne annulations by versatile C-H Activation: Mechanistic support for rhodium(III/IV)

Kong, Wei-Jun,Finger, Lars H.,Messinis, Antonis M.,Kuniyil, Rositha,Oliveira, Jo?o C.A.,Ackermann, Lutz

supporting information, p. 17198 - 17206 (2019/10/28)

A flow-metallaelectro-catalyzed C-H activation was realized in terms of robust rhodaelectro-catalyzed alkyne annulations. To this end, a modular electro-flow cell with a porous graphite felt anode was designed to ensure efficient turnover. Thereby, a variety of C-H/N-H functionalizations proved amenable for alkyne annulations with high levels of regioselectivity and functional group tolerance, viable in both an inter- or intramolecular manner. The electro-flow C-H activation allowed easy scale up, while in-operando kinetic analysis was accomplished by online flow-NMR spectroscopy. Mechanistic studies suggest an oxidatively induced reductive elimination pathway on rhodium(III) in an electrocatalytic regime.

Rhodium-Catalyzed Relay Carbenoid Functionalization of Aromatic C-H Bonds toward Fused Heteroarenes

Wu, Xiaopeng,Xiong, Hao,Sun, Song,Cheng, Jiang

supporting information, p. 1396 - 1399 (2018/03/09)

A rhodium-catalyzed annulation between ethyl benzimidates and α- aroyl sulfur ylides was developed, affording a series of pyrano[4,3,2-ij]isoquinoline derivatives in moderate to good yields with good functional group compatibility. The procedure featured

Controllable Rh(III)-Catalyzed C-H Arylation and Dealcoholization: Access to Biphenyl-2-carbonitriles and Biphenyl-2-carbimidates

Jiang, Bo,Wu, Songxiao,Zeng, Jing,Yang, Xiaobo

supporting information, p. 6573 - 6577 (2018/10/09)

A controllable Rh(III)-catalyzed C-H arylation and dealcoholization of benzimidates with arylboronic esters was developed, delivering various biphenyl-2-carbonitriles and biphenyl-2-carbimidates by simply tuning the reaction conditions. This approach features high efficiency, good functional group tolerance, and easy operation. It also provides an alternative pathway to thoroughly exploit the directing group in transition-metal-catalyzed C-H activations.

Ruthenium (II)-Catalyzed Oxidant-Free Coupling/Cyclization of Benzimidates and Sulfoxonium Ylides to Form Substituted Isoquinolines

Shi, Xinxia,Wang, Rongchao,Zeng, Xiaofei,Zhang, Yilan,Hu, Huiling,Xie, Chunsong,Wang, Min

supporting information, p. 4049 - 4053 (2018/09/21)

A ruthenium-catalyzed direct mono-C?H functionalization/annulation cascade reaction of benzimidates and sulfoxonium ylides has been developed. The reaction proceeds smoothly with a broad range of substrates, giving access to a variety of isoquinoline deri

Synthesis of Functionalized Indenones via Rh-Catalyzed C-H Activation Cascade Reaction

Lv, Ningning,Chen, Zhengkai,Liu, Yue,Liu, Zhanxiang,Zhang, Yuhong

supporting information, p. 2588 - 2591 (2017/05/24)

An efficient and expeditious protocol for the synthesis of diverse difunctionalized indenones through rhodium-catalyzed C-H activation and multistep cascade reaction of benzimidates and alkenes has been developed. The transformation involves the cleavage and formation of multiple bonds in one pot under mild reaction conditions, and Mn(OAc)2 plays an important role in the reaction.

Cobalt-Catalyzed Oxidant-Free Spirocycle Synthesis by Liberation of Hydrogen

Lv, Ningning,Liu, Yue,Xiong, Chunhua,Liu, Zhanxiang,Zhang, Yuhong

supporting information, p. 4640 - 4643 (2017/09/12)

The first example of oxidant-free cobalt-catalyzed synthesis of five-membered spirocycles is reported from benzimidates and maleimides utilizing nitrobenzene as promoter. In contrast to previously known cobalt-catalyzed oxidative C-H functionalization rea

Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis

Wang, Qiang,Li, Xingwei

supporting information, p. 2102 - 2105 (2016/06/01)

Nitrosobenzenes have been used as a convenient aminating reagent for the efficient synthesis of 1H-indazoles via rhodium and copper catalyzed C-H activation and C-N/N-N coupling. The reaction occurred under redox-neutral conditions with high efficiency and functional group tolerance. Moreover, a rhodacyclic imidate complex has been identified as a key intermediate.

Rh(III)-Catalyzed C-C/C-N Coupling of Imidates with α-Diazo Imidamide: Synthesis of Isoquinoline-Fused Indoles

Wang, He,Li, Lei,Yu, Songjie,Li, Yunyun,Li, Xingwei

supporting information, p. 2914 - 2917 (2016/07/06)

Imidate esters and diazo compounds have been established as bifunctional substrates for the construction of biologically active fused heterocycles via rhodium-catalyzed C-H activation and C-C/C-N coupling. This reaction occurs under mild conditions with high efficiency, step economy, and low catalyst loading.

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