Four-component domino reaction leading to multifunctionalized quinazolines.
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Microwave-Assisted Synthesis of Bioactive Six-Membered Heterocycles and Their Fused AnaloguesComprehensive survey of chemical libraries for drug discovery and chemical biology: 2009.Four-component domino reaction providing an easy access to multifunctionalized tricyclo[6.2.2.0(1,6)]dodecane derivatives.Thiourea dioxide promoted efficient organocatalytic one-pot synthesis of a library of novel heterocyclic compounds.A bioinspired Ugi/Michael/aza-Michael cascade reaction in aqueous media: natural-product-like molecular diversity.REGIOSELECTIVE MULTICOMPONENT DOMINO REACTIONS PROVIDING RAPID AND EFFICIENT ROUTES TO FUSED ACRIDINESFour-component bicyclization approaches to skeletally diverse pyrazolo[3,4-b]pyridine derivatives.Microwave-assisted multicomponent reaction in water leading to highly regioselective formation of benzo[f]azulen-1-ones.One-pot pseudo three-component reaction of nitroketene-N,S-acetals and aldehydes for synthesis of highly functionalized hexa-substituted 1,4-dihydropyridines.N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology.Highly selective domino multicyclizations for forming polycyclic fused acridines and azaheterocyclic skeletons.New Three-Component Bicyclization Leading to Densely Functionalized Pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidines.A multi-component domino reaction for the direct access to polyfunctionalized indoles via intermolecular allylic esterification and indolation.Metal-free [3 + 2 + 1]/[2 + 2 + 1] biscyclization: stereospecific construction with concomitant functionalization of indolizin-5(1H)-one.Efficient domino approaches to multifunctionalized fused pyrroles and dibenzo[b,e][1,4]diazepin-1-ones.Domino constructions of pentacyclic indeno[2,1-c]quinolines and pyrano[4,3-b]oxepines by [4+1]/[3+2+1]/[5+1] and [4+3] multiple cyclizations.Aerobic radical multifunctionalization of alkenes using tert-butyl nitrite and water.Allylic amination and N-arylation-based domino reactions providing rapid three-component strategies to fused pyrroles with different substituted patterns.A one-pot multicomponent strategy for stereospecific construction of tricyclic pyrrolo[1,2-a]quinolines.A novel domino strategy for forming poly-substituted quaternary imidazoles through a Cs2CO3-promoted aryl migration process.Highly efficient construction of pentacyclic benzo[b]indeno-[1,2,3-de][1,8]naphthyridine derivatives via four-component domino reaction.A new rapid multicomponent domino heteroannulation of heterocyclic ketene aminals: solvent-free regioselective synthesis of functionalized benzo[g]imidazo[1,2-a]quinolinediones.A novel three-component [5 + 1] heterocyclization leading to 2-azafluorenone synthesis and its polyfunctionalizations.A domino synthetic strategy leading to two-carbon-tethered fused acridine/indole pairs and fused acridine derivatives.A multicomponent synthetic strategy for two-carbon-tethered 1,3-oxathiole-indole pairs.New domino heteroannulation of enaminones: synthesis of diverse fused naphthyridines.
P2860
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P2860
Four-component domino reaction leading to multifunctionalized quinazolines.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
Four-component domino reaction leading to multifunctionalized quinazolines.
@en
Four-component domino reaction leading to multifunctionalized quinazolines.
@nl
type
label
Four-component domino reaction leading to multifunctionalized quinazolines.
@en
Four-component domino reaction leading to multifunctionalized quinazolines.
@nl
prefLabel
Four-component domino reaction leading to multifunctionalized quinazolines.
@en
Four-component domino reaction leading to multifunctionalized quinazolines.
@nl
P2093
P356
P1476
Four-component domino reaction leading to multifunctionalized quinazolines.
@en
P2093
Parminder Kaur
Shu-Jiang Tu
Walter Wever
P304
11660-11661
P356
10.1021/JA904011S
P407
P577
2009-08-01T00:00:00Z