Enhanced enantio- and diastereoselectivities via confinement

Photorearrangement of 2,4-cyclohexadienones included in zeolites

Sundararajan Uppili, Vaidhyanathan Ramamurthy

Research output: Contribution to journalArticle

32 Citations (Scopus)

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

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Zeolites
Enantioselectivity
Methane
zeolites
methane
selectivity
cyclohexadienone

ASJC Scopus subject areas

  • Molecular Medicine

Cite this

Enhanced enantio- and diastereoselectivities via confinement : Photorearrangement of 2,4-cyclohexadienones included in zeolites. / Uppili, Sundararajan; Ramamurthy, Vaidhyanathan.

In: Organic Letters, Vol. 4, No. 1, 10.01.2002, p. 87-90.

Research output: Contribution to journalArticle

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