Literature DB >> 20095646

Preparation of a storable zinc carbenoid species and its application in cyclopropanation, chain extension, and [2,3]-sigmatropic rearrangement reactions.

Arnaud Voituriez1, Lucie E Zimmer, André B Charette.   

Abstract

The formation of a new phosphate carbenoid (n-BuO)(2)P(O)OZnCH(2)I and its application in organozinc-mediated reactions is described. This carbenoid undergoes very slow degradation in solution and can be stored for several weeks at -20 degrees C. Its reactivity was tested with many representative alkenes and was determined to be a powerful cyclopropanating reagent, giving the corresponding cyclopropanes in 72-99% yield. The use of this carbenoid in the chain extension of 1,3-diketones and [2,3]-sigmatropic rearrangement reactions is also described.

Entities:  

Year:  2010        PMID: 20095646     DOI: 10.1021/jo902618e

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Formal and total synthesis of (±)-cycloclavine.

Authors:  Nitinkumar D Jabre; Teruki Watanabe; Matthias Brewer
Journal:  Tetrahedron Lett       Date:  2014-01-01       Impact factor: 2.415

2.  Regioselective Simmons-Smith-type cyclopropanations of polyalkenes enabled by transition metal catalysis.

Authors:  Jacob Werth; Christopher Uyeda
Journal:  Chem Sci       Date:  2018-01-02       Impact factor: 9.825

3.  Diastereodivergent combined carbometalation/zinc homologation/C-C fragmentation reaction as an efficient tool to prepare acyclic allylic quaternary carbon stereocenters.

Authors:  Sudipta Raha Roy; Dorian Didier; Amir Kleiner; Ilan Marek
Journal:  Chem Sci       Date:  2016-05-24       Impact factor: 9.825

  3 in total

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