Literature DB >> 21516181

Suzuki-Miyaura cross-coupling of 3-pyridyl triflates with 1-alkenyl-2-pinacol boronates.

James R Vyvyan1, Jennifer A Dell Née Meyer, Toby J Ligon, Kelsey K Motanic, Hayley S Wall.   

Abstract

Palladium-catalyzed Suzuki-type couplings of n class="Chemical">3-pyridyl triflates with alkenyl pinacol boronates proceed in good to excellent yield. Optimized conditions use Pd(PPh(3))(4) (10 mol %) as catalyst with K(3)PO(4) (3 equiv) as base in dioxane.

Entities:  

Year:  2010        PMID: 21516181      PMCID: PMC3080250          DOI: 10.1055/s-0030-1258237

Source DB:  PubMed          Journal:  Synthesis (Stuttg)        ISSN: 0039-7881            Impact factor:   3.157


  18 in total

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6.  Arylboronic acids and arylpinacolboronate esters in Suzuki coupling reactions involving indoles. Partner role swapping and heterocycle protection.

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7.  Pentadienyl carboxamide derivatives as antagonists of platelet-activating factor.

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Authors:  Matthieu Corbet; Michiel de Greef; Samir Z Zard
Journal:  Org Lett       Date:  2007-12-28       Impact factor: 6.005

9.  Palladium-catalyzed cross-coupling reaction of bis(pinacolato)diboron with 1-alkenyl halides or triflates: convenient synthesis of unsymmetrical 1,3-dienes via the borylation-coupling sequence.

Authors:  Jun Takagi; Kou Takahashi; Tatsuo Ishiyama; Norio Miyaura
Journal:  J Am Chem Soc       Date:  2002-07-10       Impact factor: 15.419

10.  Palladium-catalyzed borylation of phenyl bromides and application in one-pot Suzuki-Miyaura biphenyl synthesis.

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Journal:  Org Lett       Date:  2004-11-25       Impact factor: 6.005

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  1 in total

1.  Synthesis of cananodine by intramolecular epoxide opening.

Authors:  Patrick Shelton; Toby J Ligon; Jennifer M Dell Née Meyer; Loagan Yarbrough; James R Vyvyan
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  1 in total

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