Multicomponent macrocyclization reactions (MCMRs) employing highly reactive acyl ketene and nitrile oxide intermediates. - Test2 - elhamkhani - TriplyDB

Multicomponent macrocyclization reactions (MCMRs) employing highly reactive acyl ketene and nitrile oxide intermediates.

Multicomponent macrocyclization reactions (MCMRs) employing highly reactive acyl ketene and nitrile oxide intermediates.

http://www.wikidata.org/entity/Q35184388

about

Expedient synthesis of a 72-membered isoxazolino-β-ketoamide library by a 2·3-component reaction.One-Pot Approach to Organo-Phosphorus-Chalcogen Macrocycles Incorporating Double OP(S)SCn or OP(Se)SeCn Scaffolds: A Synthetic and Structural Study.

P2860

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P2860

Multicomponent macrocyclization reactions (MCMRs) employing highly reactive acyl ketene and nitrile oxide intermediates.

http://www.wikidata.org/entity/Q35184388

description

2011 nî lūn-bûn

@nan

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Multicomponent macrocyclizatio ...... d nitrile oxide intermediates.

@ast

Multicomponent macrocyclizatio ...... d nitrile oxide intermediates.

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type

label

Multicomponent macrocyclizatio ...... d nitrile oxide intermediates.

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Multicomponent macrocyclizatio ...... d nitrile oxide intermediates.

@en

prefLabel

Multicomponent macrocyclizatio ...... d nitrile oxide intermediates.

@ast

Multicomponent macrocyclizatio ...... d nitrile oxide intermediates.

@en

P1433

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P2860

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P1433

Organic Letters

P1476

Multicomponent macrocyclizatio ...... d nitrile oxide intermediates.

@en

P2093

James C Fettinger

http://www.w3.org/2001/XMLSchema#string

John M Knapp

http://www.w3.org/2001/XMLSchema#string

Mark J Kurth

http://www.w3.org/2001/XMLSchema#string

P2860

A planning strategy for diversity-oriented synthesis

New Moloka'iamine derivatives from an undescribed verongid sponge

Architectural chemistry: synthesis of topologically diverse macromulticycles by sequential multiple multicomponent macrocyclizations.

Multiple multicomponent macrocyclizations including bifunctional building blocks (MiBs) based on Staudinger and Passerini three-component reactions.

Supramolecular compounds from multiple ugi multicomponent macrocyclizations: peptoid-based cryptands, cages, and cryptophanes.

Synthesis of steroid-biaryl ether hybrid macrocycles with high skeletal and side chain variability by multiple multicomponent macrocyclization including bifunctional building blocks.

Maximizing synthetic efficiency: multi-component transformations lead the way

Designed folding of pseudopeptides: the transformation of a configurationally driven preorganization into a stereoselective multicomponent macrocyclization reaction.

Solution-phase combinatorial libraries: modulating cellular signaling by targeting protein-protein or protein-DNA interactions.

Modulation of protein-protein interactions by stabilizing/mimicking protein secondary structure elements.

P304

4732-4735

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1021/OL202024A

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P407

P433

17

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P478

13

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P577

2011-08-09T00:00:00Z

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51557526

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P698

21827181

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P932

3162989

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