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3-(3-methoxyphenyl)-3-buten-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29123-95-3

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29123-95-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29123-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29123-95:
(7*2)+(6*9)+(5*1)+(4*2)+(3*3)+(2*9)+(1*5)=113
113 % 10 = 3
So 29123-95-3 is a valid CAS Registry Number.

29123-95-3Downstream Products

29123-95-3Relevant academic research and scientific papers

Catalytic Regioselective Isomerization of 2,2-Disubstituted Oxetanes to Homoallylic Alcohols

Cabré, Albert,Lledós, Agustí,Rafael, Sergi,Riera, Antoni,Sciortino, Giuseppe,Ujaque, Gregori,Verdaguer, Xavier

supporting information, p. 7521 - 7527 (2020/03/24)

The selective isomerization of strained heterocyclic compounds is an important tool in organic synthesis. An unprecedented regioselective isomerization of 2,2-disubstituted oxetanes into homoallylic alcohols is described. The use of tris(pentafluorophenyl

Rhodium-Catalyzed Diverse Arylation of 2,5-Dihydrofuran: Controllable Divergent Synthesis via Four Pathways

Dou, Xiaowei,Hayashi, Tamio,Lu, Tao,Xing, Junhao,Ye, Bihai,Zhu, Wanjiang

, p. 2958 - 2963 (2020/03/23)

The rhodium-catalyzed controllable diverse arylation of 2,5-dihydrofuran with arylboronic acids is reported. By fine-tuning of the reaction conditions, four different ring-opening or oxidative arylation pathways are controlled in the rhodium-catalyzed ary

Photoredox-Catalyzed Cyclopropanation of 1,1-Disubstituted Alkenes via Radical-Polar Crossover Process

Luo, Wenping,Yang, Yi,Fang, Yewen,Zhang, Xinxin,Jin, Xiaoping,Zhao, Guicai,Zhang, Li,Li, Yan,Zhou, Wanli,Xia, Tingting,Chen, Bin

supporting information, p. 4215 - 4221 (2019/08/16)

The photoredox-neutral catalyzed cyclopropanation of 1,1-disubstituted alkenes via radical addition-anionic cyclization cascade has been successfully developed. Another new protocol based on photocatalytic allylation and cyclopropanation cascade was also described between allylic halide and halomethyl radical. In addition to the successful use of bis-catecholato silicates as the alkyl radical precursors, the acyl and alkyl radicals derived from 1,4-dihydropyridines were also engaged in this radical-polar crossover process. The competing experiments displayed that the 3-exo-tet mode of cyclization preferred over 4-exo and 5-exo cyclization modes, allowing for the selective 3-exo-tet cyclization. The superior nucleofuge character of bromide over chloride and tosylate has been demonstrated in the reaction of bromomethyl radical with homoallylic (pseudo)halides. This new protocol is characterized by its redox-neutral process, broad substrate scope, mild conditions, and good functional-group compatibility. (Figure presented.).

Chelation versus Non-Chelation Control in the Stereoselective Alkenyl sp2 C?H Bond Functionalization Reaction

Liang, Qiu-Ju,Yang, Chao,Meng, Fei-Fan,Jiang, Bing,Xu, Yun-He,Loh, Teck-Peng

, p. 5091 - 5095 (2017/04/24)

A hydroxy group chelation-assisted stereospecific oxidative cross-coupling reaction between alkenes was developed under mild reaction conditions. In the presence of palladium catalyst, the alkenes tethered with hydroxy functionality can couple efficiently with electron-deficient alkenes to form the corresponding multi-substituted olefin products. The hydroxy group on the substrate could play dual roles in reaction, acting as the directing group for alkenyl C?H bond activation and controlling the stereoselectivity of the products.

Enantioselective Small Molecule Synthesis by Carbon Dioxide Fixation using a Dual Br?nsted Acid/Base Organocatalyst

Vara, Brandon A.,Struble, Thomas J.,Wang, Weiwei,Dobish, Mark C.,Johnston, Jeffrey N.

supporting information, p. 7302 - 7305 (2015/06/30)

Carbon dioxide exhibits many of the qualities of an ideal reagent: it is nontoxic, plentiful, and inexpensive. Unlike other gaseous reagents, however, it has found limited use in enantioselective synthesis. Moreover, unprecedented is a tool that merges on

Tunable phosphoramidite ligands for asymmetric hydrovinylation: Ligands par excellence for generation of all-carbon quaternary centers

Smith, Craig R.,Hwan, Jung Lim,Zhang, Aibin,RajanBabu

experimental part, p. 2089 - 2100 (2010/02/28)

α-Alkylstyrenes undergo efficient hydrovinylation (addition of ethene) in the presence of a nickel catalyst prepared from [(allyl)NiBr] 2, Na+[BAr4]- [Ar = 3,5-bis(trifluoromethyl)phenyl], and a phosphoramidite ligand giving products in excellent yields and enantioselectivities. In many cases phosphoramidites derived from achiral 2,2′-biphenol are almost as good as ligands derived from the more expensive enantiopure 1,1′-bi(2-naphthol)s. The hydrovinylation products, which carry two versatile latent functionalities, an aryl and a vinyl group, are potentially useful for the synthesis of several important natural products containing benzylic all-carbon quaternary centers. Georg Thieme Verlag Stuttgart.

Regioselective Heck arylation of unsaturated alcohols by palladium catalysis in ionic liquid

Mo, Jun,Xu, Lijin,Ruan, Jiwu,Liu, Shifang,Xiao, Jianliang

, p. 3591 - 3593 (2008/09/20)

In contrast to almost all of the known examples of Heck arylation of unsaturated alcohols, which yield predominately β-arylated products, arylation under the Pd-DPPP catalysis in ionic liquid leads preferentially to aryl substitution at the α carbon, prov

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