Literature DB >> 29711449

Intramolecular Reactivity of Triplet Carbonylcarbenes.

Johannes Fien1, Wolfgang Kirmse1.   

Abstract

Through a double cyclization triplet carbonylcarbenes add smoothly to double bonds in the δ and ε position, but do not react intramolecularly with C-H bonds (see scheme). The addition reaction fails if the keto group is replaced with an ester group. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.

Entities:  

Keywords:  Carbenes; Cyclizations; Diazo compounds; Rearrangements

Year:  1998        PMID: 29711449     DOI: 10.1002/(SICI)1521-3773(19980904)37:16<2232::AID-ANIE2232>3.0.CO;2-2

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Radical Cation Cyclopropanations via Chromium Photooxidative Catalysis.

Authors:  Francisco J Sarabia; Eric M Ferreira
Journal:  Org Lett       Date:  2017-05-12       Impact factor: 6.005

  1 in total

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