Literature DB >> 11082008

Stereoselective photocycloaddition of alkenes to naphthalene rings assisted by hydrogen bonding

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Abstract

Introduction of a hydrogen-bonding substituent to 1-cyanonaphthalene and alkene resulted in the selective formations of endo-photocycloadducs. Furthermore, the yield and selectivity were improved as the reaction temperature was lowered.

Entities:  

Year:  2000        PMID: 11082008     DOI: 10.1021/ol0002368

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Solvent-controlled intramolecular [2 + 2] photocycloadditions of alpha-substituted enones.

Authors:  Stephanie M Ng; Scott J Bader; Marc L Snapper
Journal:  J Am Chem Soc       Date:  2006-06-07       Impact factor: 15.419

Review 2.  Oxetane synthesis through the Paternò-Büchi reaction.

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

  2 in total

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