Literature DB >> 18007454

Isomerization reactions of allylic alcohols into ketones with the Grubbs reagent.

Katsuyuki Nakashima1, Sanae Okamoto, Masakazu Sono, Motoo Tori.   

Abstract

Allylic alcohols were isomerized into ketones by the action of the Grubbs reagent. Some model alcohols were prepared and tested under similar conditions to reveal that less substituted alkenes rearrange more easily. More hindered alcohols are stable under these conditions, however, the simple allylic alcohols tend to isomerize producing ethyl ketone and the corresponding degraded methyl ketone.

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Year:  2004        PMID: 18007454      PMCID: PMC6147401          DOI: 10.3390/90700541

Source DB:  PubMed          Journal:  Molecules        ISSN: 1420-3049            Impact factor:   4.411


  1 in total

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Authors:  T R Hoye; H Zhao
Journal:  Org Lett       Date:  1999-07-15       Impact factor: 6.005

  1 in total
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Review 2.  Construction of eight-membered carbocycles with trisubstituted double bonds using the ring closing metathesis reaction.

Authors:  Motoo Tori; Reiko Mizutani
Journal:  Molecules       Date:  2010-06-11       Impact factor: 4.411

  2 in total

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