An approach to 1-phosphorylated isoquinolines through silver(I)-catalyzed tandem reaction involving C–N and C–P bond formation
作者:Xianbo Wang、Zhiyong Wang
DOI:10.1016/j.tet.2014.06.060
日期:2014.9
A novel silver-catalyzed tandem reaction of 2-alkynylbenzaldoximes with H-phosphinate esters, and H-phosphine oxides has been developed, providing a general and powerful tool for the synthesis of various 1-phosphorylated isoquinolins in moderate to excellent yield. This reaction proceeded smoothly to construct C–N and C–P bonds in one-pot with good functional group tolerance under mild conditions.
A silver(I)-catalyzed reaction of 2-alkynylbenzaldoxime with arylsulfonyl chloride
作者:Jinming Yang、Qing Xiao、Jie Sheng、Jie Wu
DOI:10.1016/j.tet.2013.11.056
日期:2014.1
A silver-catalyzed reaction of 2-alkynylbenzaldoxime with arylsulfonyl chloride proceeds smoothly at room temperature to afford 4-tosyloxyisoquinolines in moderate to good yields. Additionally, the resulting 4-tosyloxyisoquinolines could be further elaborated through palladium-catalyzed coupling reactions leading to diverse isoquinolines.
Aniline Dearomatization and Silver-Catalyzed [3+3] Dipolar Cycloaddition: Efficient Construction of Oxocino[4,3,2-<i>cd</i>]indoles from 2-Alkynylanilines and 2-Alkynylbenzaldoximes
作者:Dandan Han、Qiuqin He、Renhua Fan
DOI:10.1002/anie.201507277
日期:2015.11.16
2‐Alkynylanilines are attractive starting materials in indole synthesis because of their ready availability. Herein, a one‐pot stepwise procedure is reported for efficient construction of multisubstituted oxocino[4,3,2‐cd]indoles from 2‐alkynylanilines and 2‐alkynylbenzaldoximes. The method comprises the oxidative dearomatization of 2‐alkynylanilines, the silver‐catalyzed [3+3] cycloaddition with
2-炔基苯胺由于易于获得,因此在吲哚合成中是有吸引力的起始原料。本文报道了一种单步逐步程序,可从2-炔基苯胺和2-炔基苯并甲醛肟中高效构建多取代的氧代[4,3,2- cd ]吲哚。该方法包括2-炔基苯胺的氧化脱芳香化作用,2-炔基苯甲肟肟的银催化的[3 + 3]环加成反应,以及随后的热自由基骨架重排和芳构化。
1-(Isoquinolin-1-yl)urea Library Generation via Three-Component Reaction of 2-Alkynylbenzaldoxime, Carbodiimide, with Electrophile
作者:Shengqing Ye、Huanhuan Wang、Jie Wu
DOI:10.1021/co100026y
日期:2011.3.14
A novel and highly efficient three-component reaction of 2-alkynylbenzaldoxime, carbodiimide, with electrophile (bromine or iodinemonochloride) is disclosed, which generates 1-(4-haloisoquinolin-1-yl)ureas in good yields under mild conditions. Subsequent palladium-catalyzed Suzuki−Miyaura coupling reaction is introduced, leading to the diverse 1-(isoquinolin-1-yl)ureas.
Facile Synthesis of 1-(Isoquinolin-1-yl)ureas by Silver Triflate Catalyzed Tandem Reactions of 2-Alkynylbenzaldoximes with Carbodiimides
作者:Shengqing Ye、Huanhuan Wang、Jie Wu
DOI:10.1002/ejoc.201001040
日期:2010.11
2-Alkynylbenzaldoximes react with carbodiimides under mild conditions and silver triflate catalysis in DMF, leading to a diverse range of 1-(isoquinolin-1-yl)ureas in good to excellent yields. This transformation involves tandem 6-endo cyclization, [3+2] cycloaddition, and subsequent rearrangement.