Discovery of chemical reactions through multidimensional screening.
about
Synthesis and reactivity of bicyclo[3.2.1]octanoid-derived cyclopropanesTandem driven dynamic combinatorial resolution via Henry-iminolactone rearrangement.Reaction discovery employing macrocycles: transannular cyclizations of macrocyclic bis-lactamsDesign and synthesis of a library of tetracyclic hydroazulenoisoindoles.Multicomponent reaction discovery: three-component synthesis of spirooxindoles.Tandem processes identified from reaction screening: nucleophilic addition to aryl N-phosphinylimines employing La(III)-TFAA activationDevelopment of an automated microfluidic reaction platform for multidimensional screening: reaction discovery employing bicyclo[3.2.1]octanoid scaffolds.Reaction discovery using microfluidic-based multidimensional screening of polycyclic iminium ethers.Discovery of new antimalarial chemotypes through chemical methodology and library developmentGold catalyzed cyclization of alkyne-tethered dihydropyrimidonesMicrowave-based reaction screening: tandem retro-Diels-Alder/Diels-Alder cycloadditions of o-quinol dimers.Three-component reaction discovery enabled by mass spectrometry of self-assembled monolayersRemodelling of the natural product fumagillol employing a reaction discovery approachSynthesis of azaphilone-based chemical librariesSmall molecules of different origins have distinct distributions of structural complexity that correlate with protein-binding profiles.A Reactivity-Driven Approach to the Discovery and Development of Gold-Catalyzed Organic Reactions.Expanding the chemical diversity of spirooxindoles via alkylative pyridine dearomatization.Synthesis of a novel chemotype via sequential metal-catalyzed cycloisomerizations.Label-assisted mass spectrometry for the acceleration of reaction discovery and optimizationMultidimensional reaction screening for photochemical transformations as a tool for discovering new chemotypes.Multidimensional Screening and Methodology Development for Condensations Involving Complex 1,2-Diketones.Novel selection methods for DNA-encoded chemical librariesEnzyme immunoassays as screening tools for catalysts and reaction discovery.Discovery of an α-amino C-H arylation reaction using the strategy of accelerated serendipity.Suzuki-Miyaura cross-coupling optimization enabled by automated feedback.Hits, leads and drugs against malaria through diversity-oriented synthesis.Experiment and computation: a combined approach to study the reactivity of palladium complexes in oxidation states 0 to IV.Contemporary screening approaches to reaction discovery and development.A simple, multidimensional approach to high-throughput discovery of catalytic reactions.Development and initial application of a hybridization-independent, DNA-encoded reaction discovery system compatible with organic solvents.Ruthenium(0)-Catalyzed [4+2] Cycloaddition of Acetylenic Aldehydes with α-Ketols: Convergent Construction of Angucycline Ring Systems.A biomolecule-compatible visible-light-induced azide reduction from a DNA-encoded reaction-discovery system.Gold-catalyzed dealkoxylative carbocyclization/[3+3] annulation cascade of acetal-allene or ketal-allene substrates.Gold-catalyzed annulations of 2-alkynyl benzaldehydes with vinyl ethers: synthesis of dihydronaphthalene, isochromene, and bicyclo[2.2.2]octane derivatives.Chiral silver phosphate catalyzed transformation of ortho-alkynylaryl ketones into 1H-isochromene derivatives through an intramolecular-cyclization/enantioselective-reduction sequence.Discovery of chemoselective and biocompatible reactions using a high-throughput immunoassay screening.Identifying lead hits in catalyst discovery by screening and deconvoluting complex mixtures of catalyst components.Asymmetric Hydrogenation of In Situ Generated Isochromenylium Intermediates by Copper/Ruthenium Tandem Catalysis.Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes.Metal-Free Reaction of ortho-Carbonylated Alkynyl-Substituted Arylaldehydes with Common Amines: Selective Access to Functionalized Isoindolinone and Indenamine Derivatives.
P2860
Q31039385-0A54E4A1-7658-4400-BB75-5BFA108418B3Q33334544-9F9D9C55-03EC-47BB-94E8-9CC19D2214D6Q33395058-98375640-1913-4F11-8B95-4916D0664081Q33430104-D83B0E4D-28A5-4FEC-8E96-F8876F4725F2Q33521994-EFD3726A-A63D-45D4-9B2E-6F403E3ACDDFQ33556089-8DC88733-BDB9-4335-8C21-215B8C92EA5DQ33609001-70F2014F-4925-4088-B919-2879DB0252AFQ33757765-332C49BD-1469-4FFB-9DE4-07A7D3D7DC1BQ33875149-C0D19552-D0E9-4D0C-8112-7A9B7EDF7CDCQ33958635-B0384E3E-3536-4026-8E13-3F1B55061A27Q34028663-5FC6C979-59EE-4C24-AC38-52C4075A1FD9Q34101287-CCBA221A-6A14-47A5-833F-FA1E58B9E5DBQ34116181-C23BB7AA-3C8A-4FAC-AB77-41A5F47B6A47Q34157614-4FFDC851-AAB5-475A-9345-C5A0CE5FC61CQ34279373-4E9F16C3-8098-4578-8F66-FBE41D4ADC36Q34377834-C5025A0F-86FF-403B-9960-81FB676D5BB0Q34423589-FBE2F481-FDEA-432A-9273-D3F1B5135AB2Q34423625-851A850C-7694-4C90-A3DA-BDB443C2202EQ34681107-C3E52249-7145-42B5-B2C5-270E2198187FQ35138910-50859B3A-6747-4891-8F58-334348685BBDQ35226934-E9F29587-9E34-44C0-80E2-DBD4AE5D0533Q35568757-615AA6A3-0C8D-4A97-8586-3DDC0020276CQ35576136-FAE5FAA7-9E93-49D9-B022-5BF5BAC50723Q35697679-B3B54AB4-153B-437A-B9B3-B881DC797F32Q37441389-DA56CAF3-D243-4920-AF9C-826E2EDBB9D2Q38066992-B53601A3-0D7E-4762-83C3-7B1CF61F44A1Q38206709-BFBF954F-E045-496C-B886-24ECFC4BF336Q38253009-75DA8D38-319A-47E9-9E26-786ECF95E33DQ40517049-E9641B86-448A-4EB1-8C17-66E1A470B41EQ41812718-2B45DA80-EBD2-49A2-AA5D-DA6261B6FA00Q41875924-B4A2D5A6-56D4-4C87-ADC3-EBE671DA1EDAQ42717961-C3FFFBE8-9827-4F1D-B33D-BF756BD6B892Q43121346-C12768F1-251E-4625-A10F-2C1407A24FF7Q43864271-6DFB7F7D-D432-4AC2-996B-074173BC0C23Q44219269-D429B692-C2ED-45FA-A139-4A359B6F9309Q45731462-74F6A5D7-6031-4015-853E-7C6D259BD6CDQ47097760-12D58A06-3AC1-4D05-AFFE-FAF7D76DD9D2Q48123291-A29BE486-52E8-4C8A-82C0-CD47E2360F19Q48210651-337A6058-1BAD-4F1B-B88F-334711204843Q48304506-521C0366-0C5F-44F4-A9AB-9B02B188BEE8
P2860
Discovery of chemical reactions through multidimensional screening.
description
2007 nî lūn-bûn
@nan
2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Discovery of chemical reactions through multidimensional screening.
@ast
Discovery of chemical reactions through multidimensional screening.
@en
Discovery of chemical reactions through multidimensional screening.
@nl
type
label
Discovery of chemical reactions through multidimensional screening.
@ast
Discovery of chemical reactions through multidimensional screening.
@en
Discovery of chemical reactions through multidimensional screening.
@nl
prefLabel
Discovery of chemical reactions through multidimensional screening.
@ast
Discovery of chemical reactions through multidimensional screening.
@en
Discovery of chemical reactions through multidimensional screening.
@nl
P2093
P356
P1476
Discovery of chemical reactions through multidimensional screening.
@en
P2093
Aaron B Beeler
John A Porco
P304
P356
10.1021/JA0674744
P407
P577
2007-02-01T00:00:00Z