Synthesis of 2-(Isoquinolin-1-yl)prop-2-en-1-ones via Silver(I)-Catalyzed One-Pot Tandem Reaction of <i>ortho</i>-Alkynylbenzaldoximes with Propargylic Alcohols
作者:Ali Nikbakht、Saeed Balalaie、Bernhard Breit
DOI:10.1021/acs.orglett.9b02952
日期:2019.9.20
The silver(I)-catalyzed reaction of ortho-alkynylbenzaldoximes with propargylic alcohols represents a new strategy for the divergent one-pot synthesis of 2-(isoquinolin-1-yl) prop-2-en-1-ones viatandem 6-endo-cyclization, 1,3-dipolar cycloaddition, and intramolecular dehydrative opening of the 2,3-dihydroisoxazole ring. This synthetic protocol tolerates a wide variety of ortho-alkynylbenzaldoximes
Synthesis of <i>N</i>-(Isoquinolin-1-yl)sulfonamides via Ag<sub>2</sub>O-Catalyzed Tandem Reaction of <i>ortho</i>-Alkynylbenzaldoximes with Benchtop Stabilized Ketenimines
this project, a moderately efficient approach to multisubstituted N-(isoquinolin-1-yl)sulfonamide derivatives was illustrated, utilizing ortho-alkynylbenzaldoximes and zwitterionic ketenimine salts in a tandem reaction catalyzed by silver oxide. The oxophilicity of Ag2O, along with its nature as Lewisacid, pave the way for a smooth [3 + 2] cycloaddition between isoquinoline N-oxides and ketenimine species
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。