Bai, Xu-Guan’s team published research in Organic Letters in 2020-07-02 | 90806-58-9

Organic Letterspublished new progress about Addition reaction. 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Name: 5-Methoxyisoquinoline.

Bai, Xu-Guan; Miao, Hong-Jie; Zhao, Yang; Wang, Qi-Lin; Bu, Zhan-Wei published the artcile< Regioselective and Diastereoselective Dearomative Multifunctionalization of In-Situ-Activated Azaarenes: An Access to Bridged Azaheterocycles>, Name: 5-Methoxyisoquinoline, the main research area is polycyclic bridged azaheterocycle regioselective diastereoselective synthesis; dearomative ring opening closure sequence polycyclic bridged azaheterocycle preparation.

Reported herein is an unprecedented multicomponent one-pot dearomative multifunctionalization of com. available azaarenes through an in situ activation strategy, which not only achieved the first full exploitation of the reactive sites of the azaarenes, but also accomplished the efficient synthesis of bridged hydrogenated pyridines and (iso)quinolines in a highly regioselective and diastereoselective manner. In addition, we could successfully realize the step-controlled dearomative trifunctionalization and bifunctionalization of quinolines.

Organic Letterspublished new progress about Addition reaction. 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Name: 5-Methoxyisoquinoline.

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem

 

Dong, Jianyang’s team published research in Green Chemistry in 2021 | 90806-58-9

Green Chemistrypublished new progress about Alcohols Role: SPN (Synthetic Preparation), PREP (Preparation) (heteroarylethyl). 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Quality Control of 90806-58-9.

Dong, Jianyang; Yue, Fuyang; Liu, Jianhua; Song, Hongjian; Liu, Yuxiu; Wang, Qingmin published the artcile< Visible-light-mediated three-component Minisci reaction for heteroarylethyl alcohols synthesis>, Quality Control of 90806-58-9, the main research area is heteroarylethyl alc green diastereoselective preparation; heteroaryl alkene three component Minisci visible light iridium catalyst.

Herein, a mild, modular, practical Minisci reaction for catalytic synthesis of heteroarylethyl alcs. such as ArCH(R1)CHR2OH [Ar = quinol-2-yl, isoquinolin-1-yl, 2-benzothiazolyl, etc.; R1R2 = CH2(CH2)2CH2, CH2CH2CH2; R1 = On-Bu, Me; R2 = H, Me] via sequential addition of H2O and N-heteroarenes across olefinic double bonds was reported. This scalable protocol was used for direct hydroxy-heteroarylation of olefins with a wide range of N-heteroarenes and could be expected to permit rapid conversion of abundant feedstock materials into medically relevant mols.

Green Chemistrypublished new progress about Alcohols Role: SPN (Synthetic Preparation), PREP (Preparation) (heteroarylethyl). 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Quality Control of 90806-58-9.

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem

 

Li, Tao’s team published research in Organic Letters in 2020-03-20 | 90806-58-9

Organic Letterspublished new progress about 1,3-Dicarbonyl compounds Role: RCT (Reactant), RACT (Reactant or Reagent). 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Product Details of C10H9NO.

Li, Tao; Liang, Kangjiang; Zhang, Yang; Hu, Dongyan; Ma, Zhixian; Xia, Chengfeng published the artcile< Three-Component Minisci Reaction with 1,3-Dicarbonyl Compounds Induced by Visible Light>, Product Details of C10H9NO, the main research area is quinoline preparation visible light Minisci dicarbonyl vinyl ether heterocycle; isoquinoline preparation visible light Minisci dicarbonyl vinyl ether heterocycle.

A three-component Minisci reaction coupling of 1,3-dicarbonyl compounds with vinyl ethers and quinolines or isoquinolines under visible light is developed. The 1,3-dicarbonyl compound undergoes single-electron oxidation to afford an electrophilic 1,3-dicarbonyl radical under visible light irradiation Due to the polarity of the free radical, the electrophilic radical adds to the electron-rich olefin to afford the nucleophilic radical. It coupled with the heteroarene to afford the three-component coupling products.

Organic Letterspublished new progress about 1,3-Dicarbonyl compounds Role: RCT (Reactant), RACT (Reactant or Reagent). 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Product Details of C10H9NO.

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem

 

Xie, Hongling’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2022 | 90806-58-9

Chemical Communications (Cambridge, United Kingdom)published new progress about Allylic alcohols Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Synthetic Route of 90806-58-9.

Xie, Hongling; Yang, Zhenkun; Tang, Luning; Han, Zhengyu; Sun, Jianwei; Huang, Hai published the artcile< Construction of nine-membered N,N,O-heterocycles via Pd-catalyzed [6+3] dipolar cycloaddition>, Synthetic Route of 90806-58-9, the main research area is vinyl oxetane iminoisoquinolinium ylide palladium catalyst dipolar cycloaddition; tetrahydrooxadiazoninoisoquinoline preparation.

A new approach for the synthesis of 9-membered N,N,O-heterocycles by Pd-catalyzed [6+3] dipolar cycloaddition of N-iminoisoquinolinium ylides and 2-vinyl oxetanes was developed. The scope of this cycloaddition was demonstrated with 28 examples. This was another important synthetic strategy for medium-sized rings by employing N-iminoisoquinolinium ylides as ternary synthons.

Chemical Communications (Cambridge, United Kingdom)published new progress about Allylic alcohols Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 90806-58-9 belongs to class isoquinoline, and the molecular formula is C10H9NO, Synthetic Route of 90806-58-9.

Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem