Literature DB >> 29493826

Cooperative Iodide Pd(0)-Catalysed Coupling of Alkoxyallenes and N-Tosylhydrazones: A Selective Synthesis of Conjugated and Skipped Dienes.

Stefano Parisotto1, Lorenzo Palagi1, Cristina Prandi1, Annamaria Deagostino1.   

Abstract

Palladium(0)-catalysed hydro-alkylation or -alkenylation of alkoxyallenes with N-tosylhydrazones gives direct access to conjugated and skipped 1-alkoxydienes with high efficiency and excellent functional-group compatibility. The reaction is proposed to involve the in situ-formed t-butanol as proton source in the key step of the allylpalladium(II) species generation. Moreover, lithium iodide or iodobenzene are employed as an unprecedented iodide (I- ) reservoir to sustain the catalytic cycle.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkoxyallenes; dienes; iodide; palladium; tosylhydrazones

Year:  2018        PMID: 29493826     DOI: 10.1002/chem.201800765

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


  1 in total

1.  Pd-Catalyzed Heck-Type Reactions of Allenes for Stereoselective Syntheses of Substituted 1,3-Dienes.

Authors:  Logan E Vine; Jennifer M Schomaker
Journal:  Chemistry       Date:  2021-11-11       Impact factor: 5.236

  1 in total

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