Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.

Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.

Item
http://www.wikidata.org/entity/Q43112615
Methionine and seleno-methionine type peptide and peptoid building blocks synthesized by five-component five-center reactions.Higher-order multicomponent reactions: beyond four reactants.A chemoselective Ugi-type reaction in water using TMSCN as a functional isonitrile equivalent: generation of heteroaromatic molecular diversity.Multicomponent reaction design in the quest for molecular complexity and diversity.Application of heterocyclic aldehydes as components in Ugi-Smiles couplingsSynthesis of acylhydrazino-peptomers, a new class of peptidomimetics, by consecutive Ugi and hydrazino-Ugi reactionsSynthesis of structurally diverse 3,4-dihydropyrimidin-2(1H)-ones via sequential Biginelli and Passerini reactions.Multicomponent versus domino reactions: One-pot free-radical synthesis of β-amino-ethers and β-amino-alcohols.A transition metal-free tandem process to pyridazinopyrido[3,2-f][1,4]thiazepine-diones via Smiles rearrangement.A four-component reaction involving in situ generated organometallic reagents: straightforward access to β-amino esters.Ceric ammonium nitrate (CAN): an efficient and eco-friendly catalyst for the one-pot synthesis of alkyl/aryl/heteroaryl-substituted bis(6-aminouracil-5-yl)methanes at room temperatureSodium Formate-Catalyzed One-Pot Synthesis of Benzopyranopyrimidines and 4-Thio-substituted 4H-Chromenes via Multicomponent Reaction at Room TemperatureEco-friendly, One-Pot Multicomponent Synthesis of Pyran Annulated Heterocyclic Scaffolds at Room Temperature Using Ammonium or Sodium Formate as Non-toxic Catalystl-Proline catalyzed multicomponent one-pot synthesis of gem-diheteroarylmethane derivatives using facile grinding operation under solvent-free conditions at room temperatureNano-Mgo-Catalyzed One-Pot Synthesis of Phosphonate Ester Functionalized 2-Amino-3-Cyano-4H-Chromene Scaffolds at Room TemperatureOne-Pot Synthesis of 3-[(N-Alkylanilino)(aryl)methyl]indoles via a Transition Metal Assisted Three-Component Condensation at Room TemperatureHighly active magnetically separable CuFe2O4 nanocatalyst: an efficient catalyst for the green synthesis of tetrahydrofuro[3,4-b]quinoline-1,8(3H,4H) dione derivatives
P2860

Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.

Item
http://www.wikidata.org/entity/Q43112615
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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name
Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.
@en
Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.
@nl
type
label
Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.
@en
Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.
@nl
prefLabel
Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.
@en
Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P577
P698
P356
P1433
P1476
Seven-component reactions by sequential chemoselective Ugi-Mumm/Ugi-Smiles reactions.
@en
P2093
P304
P31
P356
P407
P433
P478
P577
P698