Literature DB >> 20967355

Pd-catalyzed 5-endo-trig-type cyclization of β,γ-unsaturated carbonyl compounds: an efficient ring closing reaction to give γ-butenolides and 3-pyrrolin-2-ones.

Gan B Bajracharya1, Priti S Koranne, Rashid N Nadaf, Randa Kassem Mohamed Gabr, Kazuhiro Takenaka, Shinobu Takizawa, Hiroaki Sasai.   

Abstract

The 5-endo-trig-type cyclization has been performed using a Pd-bis(isoxazoline) catalyst. The present cyclization of β,γ-unsaturated carbonyl compounds gave γ-butenolides and 3-pyrrolin-2-ones in good to excellent yields.

Entities:  

Year:  2010        PMID: 20967355     DOI: 10.1039/c0cc02352c

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


  1 in total

1.  Guiding a divergent reaction by photochemical control: bichromatic selective access to levulinates and butenolides.

Authors:  Revannath L Sutar; Saumik Sen; Or Eivgi; Gal Segalovich; Igor Schapiro; Ofer Reany; N Gabriel Lemcoff
Journal:  Chem Sci       Date:  2017-12-18       Impact factor: 9.825

  1 in total

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