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

Sundararajan Uppili, V. Ramamurthy

Research output: Contribution to journalArticle

35 Scopus citations

Abstract

(figure presented) 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-π-methane rearrangement of 2,4-cyclohexadienones.

Original languageEnglish (US)
Pages (from-to)87-90
Number of pages4
JournalOrganic letters
Volume4
Issue number1
DOIs
StatePublished - Jan 10 2002
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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