Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library - Wikidata - awgldk - TriplyDB

Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library

Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library

http://www.wikidata.org/entity/Q33857987

about

Natural products as sources of new drugs over the 30 years from 1981 to 2010 Towards the systematic exploration of chemical space.Diversity-oriented synthesis: producing chemical tools for dissecting biology.Accessing a small library of pluripotent 1,4,5-trisubstituted 1H-1,2,3-triazoles via diversity-oriented synthesis.Biomimetic diversity-oriented synthesis of benzannulated medium rings via ring expansion Cheminformatic comparison of approved drugs from natural product versus synthetic origins.Versatile method for the detection of covalently bound substrates on solid supports by DART mass spectrometry.Asymmetric synthesis of amines using tert-butanesulfinamide.Asymmetric synthesis of propargylamines as amino acid surrogates in peptidomimetics.Assembly of Terpenoid Cores by a Simple, Tunable Strategy.Peptidines: glycine-amidine-based oligomers for solution- and solid-phase synthesis† †Electronic supplementary information (ESI) available: Experimental procedures, characterization data of new compounds. CCDC 1430515. For ESI and crystallographic d

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Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library

http://www.wikidata.org/entity/Q33857987

description

2011 nî lūn-bûn

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Solid-phase synthesis and chem ...... lkaloid/terpenoid-like library

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Solid-phase synthesis and chem ...... lkaloid/terpenoid-like library

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type

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Solid-phase synthesis and chem ...... lkaloid/terpenoid-like library

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PNAS.1015268108

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Solid-phase synthesis and chem ...... lkaloid/terpenoid-like library

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P2093

Christine M Diblasi

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Derek S Tan

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

Renato A Bauer

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P2860

Privileged scaffolds for library design and drug discovery

Enyne metathesis (enyne bond reorganization)

Reagent based DOS: a "Click, Click, Cyclize" strategy to probe chemical space

Natural products and combinatorial chemistry: back to the future.

Libraries from natural product-like scaffolds.

Pathway development and pilot library realization in diversity-oriented synthesis: exploring Ferrier and Pauson-Khand reactions on a glycal template.

A library of spirooxindoles based on a stereoselective three-component coupling reaction.

Molecular shape diversity of combinatorial libraries: a prerequisite for broad bioactivity.

Diversity-oriented synthesis: exploring the intersections between chemistry and biology.

Solid-supported [2+2+2] cyclotrimerizations.

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6745-6750

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10.1073/PNAS.1015268108

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17

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108

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Gustavo Moura-Letts

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50936574

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