Literature DB >> 18816555

Stannylated polynorbornenes as new reagents for a clean Stille reaction.

Nora Carrera1, Enrique Gutiérrez, Rut Benavente, M Mar Villavieja, Ana C Albéniz, Pablo Espinet.   

Abstract

New functionalized polynorbornenes have been obtained in good yields by vinylic copolymerization of norbornene with a (norbornenyl)SnBu(2)Cl monomer, catalyzed by [Ni(C(6)F(5))(2)(SbPh(3))(2)]. Subsequent functionalization produces a wide variety of polymers with different --SnBu(2)R groups (R=aryl, vinyl, alkynyl). The polymers can be used as R-transfer reagents in Stille couplings, thereby providing easy workup and separation of the polymeric tin byproducts from the coupling products. Tin contents of around 0.05 wt % are found in the Stille products. The stannylated polymers can be recycled and reused with good efficiency.

Entities:  

Year:  2008        PMID: 18816555     DOI: 10.1002/chem.200800558

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Antioxidant activity of butyl- and phenylstannoxanes derived from 2-, 3- and 4-pyridinecarboxylic acids.

Authors:  Alicia Corona-Bustamante; Juan Manuel Viveros-Paredes; Angelina Flores-Parra; Ana Lilia Peraza-Campos; Francisco J Martínez-Martínez; María Teresa Sumaya-Martínez; Angel Ramos-Organillo
Journal:  Molecules       Date:  2010-08-09       Impact factor: 4.411

2.  A different polynorbornene backbone by combination of two polymer growth pathways: vinylic addition and ring opening via β-C elimination.

Authors:  Ignacio Pérez-Ortega; Ana C Albéniz
Journal:  Chem Sci       Date:  2022-01-20       Impact factor: 9.825

3.  Synthesis of Polyflourinated Biphenyls; Pushing the Boundaries of Suzuki-Miyaura Cross Coupling with Electron-Poor Substrates.

Authors:  David Bulfield; Stefan M Huber
Journal:  J Org Chem       Date:  2017-12-04       Impact factor: 4.354

  3 in total

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