Stereoselective formation of a functionalized dipeptide isostere by zinc carbenoid-mediated chain extension. - Wikidata - awgldk - TriplyDB

Stereoselective formation of a functionalized dipeptide isostere by zinc carbenoid-mediated chain extension.

Stereoselective formation of a functionalized dipeptide isostere by zinc carbenoid-mediated chain extension.

http://www.wikidata.org/entity/Q37186632

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A compendium of cyclic sugar amino acids and their carbocyclic and heterocyclic nitrogen analogues.The tandem chain extension aldol reaction used for synthesis of ketomethylene tripeptidomimetics targeting hPEPT1 Syntheses of papyracillic acids: application of the tandem chain extension-acylation reaction

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P2860

Stereoselective formation of a functionalized dipeptide isostere by zinc carbenoid-mediated chain extension.

http://www.wikidata.org/entity/Q37186632

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Stereoselective formation of a ...... noid-mediated chain extension.

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Stereoselective formation of a ...... noid-mediated chain extension.

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Stereoselective formation of a ...... noid-mediated chain extension.

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Stereoselective formation of a ...... noid-mediated chain extension.

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prefLabel

Stereoselective formation of a ...... noid-mediated chain extension.

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Stereoselective formation of a ...... noid-mediated chain extension.

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Journal of Organic Chemistry

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Stereoselective formation of a ...... noid-mediated chain extension.

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Charles K Zercher

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Cory R Theberge

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Jerry Jasinski

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Timothy J Henderson

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Weimin Lin

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645-651

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scholarly article

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10.1021/JO801993K

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2

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74

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23570323

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19055379

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stereoselectivity

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2680025

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