Literature DB >> 11772097

Enhanced enantio- and diastereoselectivities via confinement: photorearrangement of 2,4-cyclohexadienones included in zeolites.

Sundararajan Uppili1, V Ramamurthy.   

Abstract

[reaction: see text] Employing zeolite as the reaction medium, it is possible to change the enantio (from achiral dienones) and diastereo (from chiral dienones) selectivities during the oxa-di-pi-methane rearrangement of 2,4-cyclohexadienones.

Entities:  

Year:  2002        PMID： 11772097     DOI： 10.1021/ol010245w

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


  3 in total

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Authors:  Matthew J Genzink; Jesse B Kidd; Wesley B Swords; Tehshik P Yoon
Journal:  Chem Rev       Date:  2021-10-04       Impact factor: 60.622

2.  Lewis Acid Catalyzed Enantioselective Photochemical Rearrangements on the Singlet Potential Energy Surface.

Authors:  Malte Leverenz; Christian Merten; Andreas Dreuw; Thorsten Bach
Journal:  J Am Chem Soc       Date:  2019-12-16       Impact factor: 15.419

Review 3.  Achiral Zeolites as Reaction Media for Chiral Photochemistry.

Authors:  Vaidhyanathan Ramamurthy
Journal:  Molecules       Date:  2019-10-02       Impact factor: 4.411
  3 in total

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