Literature DB >> 15064785

Stereoselective generation of vicinal stereogenic quaternary centers by photocycloaddition of 5-methoxy oxazoles to alpha-keto esters: synthesis of erythro beta-hydroxy dimethyl aspartates.

Axel G Griesbeck1, Samir Bondock, Johann Lex.   

Abstract

The photocycloaddition of methyl pyruvate and methyl phenylglyoxylate, respectively, to 5-methoxy oxazoles bearing additional substituents at C-2 and C-4 leads to bicyclic oxetanes 2 and 3 with high to moderate (exo) diastereoselectivity that can be easily ring-opened to give bis-quaternary aspartic acid diester derivatives 4 and 5.

Entities:  

Year:  2004        PMID: 15064785     DOI: 10.1039/b401990c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Continuous flow based catch and release protocol for the synthesis of alpha-ketoesters.

Authors:  Alessandro Palmieri; Steven V Ley; Anastasios Polyzos; Mark Ladlow; Ian R Baxendale
Journal:  Beilstein J Org Chem       Date:  2009-05-20       Impact factor: 2.883

2.  Photocycloaddition of aromatic and aliphatic aldehydes to isoxazoles: Cycloaddition reactivity and stability studies.

Authors:  Axel G Griesbeck; Marco Franke; Jörg Neudörfl; Hidehiro Kotaka
Journal:  Beilstein J Org Chem       Date:  2011-01-26       Impact factor: 2.883

Review 3.  Oxetane synthesis through the Paternò-Büchi reaction.

Authors:  Maurizio D'Auria; Rocco Racioppi
Journal:  Molecules       Date:  2013-09-16       Impact factor: 4.411

  3 in total

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