about
One pot synthesis of selenocysteine containing peptoid libraries by Ugi multicomponent reactions in waterA bioinspired Ugi/Michael/aza-Michael cascade reaction in aqueous media: natural-product-like molecular diversity.Carbohydrates as a reagent in multicomponent reactions: one-pot access to a new library of hydrophilic substituted pyrimidine-fused heterocycles.Facile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines.Asymmetric multicomponent reactions (AMCRs): the new frontier.Regioselective Synthesis of a Family of β-Lactams Bearing a Triazole Moiety as Potential Apoptosis InhibitorsSolid-phase and microwave-assisted syntheses of 2,5-diketopiperazines: small molecules with great potentialOrganic synthesis "on water".Bis[(l)prolinate-N,O]Zn: A water-soluble and recycle catalyst for various organic transformations.Green chemistry oriented organic synthesis in water.Recent developments in asymmetric multicomponent reactions.Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics.Groebke-Blackburn-Bienaymé multicomponent reaction: emerging chemistry for drug discovery.Direct Substitution of Alcohols in Pure Water by Brønsted Acid Catalysis.Stereochemical control of the Passerini reactionBenign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis.A Bifunctional Fluorogenic Rhodamine Probe for Proximity-Induced Bioorthogonal Chemistry.Unique alternating peptide-peptoid copolymers from dipeptides via a Ugi reaction in water.Multistructural microiteration technique for geometry optimization and reaction path calculation in large systems.On the role of interfacial hydrogen bonds in "on-water" catalysis.Highly efficient "on water" catalyst-free nucleophilic addition reactions using difluoroenoxysilanes: dramatic fluorine effects.Organocatalytic asymmetric epoxidation and tandem epoxidation/Passerini reaction under eco-friendly reaction conditions.Efficient Friedel-Crafts alkylation of indoles and pyrrole with enones and nitroalkene in water.Atom-Economic Synthesis of 4-Pyrones from Diynones and Water.One-Pot Multicomponent Synthesis of β-Amino Amides.Exploring isonitrile-based click chemistry for ligation with biomolecules.Supramolecular Organocatalysis in Water Mediated by Macrocyclic Compounds.Multicomponent polysaccharide-protein bioconjugation in the development of antibacterial glycoconjugate vaccine candidates.Versatile side chain modification via isocyanide-based multicomponent reactions: tuning the LCST of poly(2-oxazoline)sReactions of hydrophobic organic nanoparticle mixtures in water: nanoparticle-on-nanoparticle oxidative dye bleachingMulticomponent Reactions Accelerated by Aqueous Micelles“On Water” Sonochemical Multicomponent Synthesis of Novel Bioactive 1,1′-(Aryl)bis(2-(cyclohexylamino)-2-oxoethane-1,1-diyl) Di(alkanoates and benzoates)
P2860
Q28194628-9F1D7B0C-30A2-4ABA-9B60-6C9C5E6BA723Q34030880-A86D8035-A318-41E8-953D-064CCF745955Q35333827-1E80FC0B-DD42-41BD-ACB4-566F714A716AQ35848935-2900DF75-BCF2-4F0F-A0C2-F5041D3E7B48Q36047385-923B0B5A-F3E4-4AB8-95AA-5EAAA2820285Q36173636-0DAB32FF-2C7A-4DE3-9200-611081D6AED5Q37089937-CFC9B053-8B63-4958-B683-E1FEE769BC50Q37390577-667914EE-9290-4EA0-8495-D857D069F112Q37682706-92C57518-354F-4DA9-B140-34E8DA7732D8Q37952065-FBEBCB60-E294-425C-9B9A-FFD64CC9094CQ38006603-691592D7-DA3B-4EE1-B465-3BD856FBE353Q38194138-34F3E8DA-4535-4944-B8CB-FABADA816A44Q38504430-75E9BBA6-9A8B-4B84-B6C5-467E78C648D3Q39214910-F8F3E6C7-95F3-4CBC-BDB9-03FE2002CBD1Q42794138-F874F8DD-FC2C-46DE-92D4-A1EBD32006F4Q44767766-291CE345-35A0-43A5-8F56-0DDEFEF7BC45Q47634321-A00D9420-9D97-45E3-AF91-319F41B8404BQ47819839-9159A0F0-C1FF-4D9C-946B-EB7DBB8BC50EQ48059114-2C2F37CA-B792-41EF-8052-95E898A68E58Q50048776-E4344E76-C438-4F1A-BABC-F3B52DA03F15Q50452684-6F9A6892-DD81-4980-9642-1AD2F8547BC1Q50491750-CF6229F8-D854-4AD9-A53A-7C64AC468986Q50708197-4F00835F-A125-4BC8-A0C8-B6D192E03D00Q51050573-DF9DEB54-33E8-4D11-A5C2-624499368E53Q52698369-34ACDF49-3CEF-4305-A447-C086728A5526Q55054879-5DA48DA0-8D17-4595-8AFB-652368058E93Q55174689-B914FBDD-8FB0-4AE5-A38A-42AEB1BB4A69Q55331828-E65947AA-A66D-468F-ACB6-89AC386FD18EQ57368593-B4F0C00E-B2AC-4F43-BD74-330D4C8EB7EEQ58073624-BD4549A4-CC78-4251-A3B5-213F46FE082AQ58580341-06C19046-147B-4027-8C68-7249E755BC03Q59008767-3CB4CE90-FD03-4BAB-A244-243C4B3B9E8F
P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Multicomponent reactions are accelerated in water.
@ast
Multicomponent reactions are accelerated in water.
@en
type
label
Multicomponent reactions are accelerated in water.
@ast
Multicomponent reactions are accelerated in water.
@en
prefLabel
Multicomponent reactions are accelerated in water.
@ast
Multicomponent reactions are accelerated in water.
@en
P356
P1476
Multicomponent reactions are accelerated in water.
@en
P2093
Koushik Das Sarma
Michael C Pirrung
P304
P356
10.1021/JA038583A
P407
P577
2004-01-01T00:00:00Z