Literature DB >> 12357770

An efficient synthesis of endo,exo-furofuranone derivatives.

Nigel A Swain1, Richard C D Brown, Gordon Bruton.   

Abstract

The ring openings of 1-acetyl-4-phenyl-3-oxabicyclo[3.1.0]hexane afforded alpha-acetyl-gamma-butyrolactone that underwent a novel diazo-transfer reaction, followed by C-H insertion, to provide a series of endo,exo-furofuranone analogues.

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Year:  2002        PMID: 12357770     DOI: 10.1039/b206150c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Rh-catalyzed intermolecular reactions of cyclic α-diazocarbonyl compounds with selectivity over tertiary C-H bond migration.

Authors:  Andrew DeAngelis; Olga Dmitrenko; Joseph M Fox
Journal:  J Am Chem Soc       Date:  2012-06-19       Impact factor: 15.419

2.  Extending the Salinilactone Family.

Authors:  Christian Schlawis; Tim Harig; Stephanie Ehlers; Dulce G Guillen-Matus; Kaitlin E Creamer; Paul R Jensen; Stefan Schulz
Journal:  Chembiochem       Date:  2020-03-10       Impact factor: 3.164

Review 3.  Preparation and Synthetic Applications of Five-to-Seven-Membered Cyclic α-Diazo Monocarbonyl Compounds.

Authors:  Daniil Zhukovsky; Dmitry Dar'in; Olga Bakulina; Mikhail Krasavin
Journal:  Molecules       Date:  2022-03-21       Impact factor: 4.411

  3 in total

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