Short path syntheses of α-diozonides by sequential ozonolyses of acetylenes and O-methyl oximes

Yuxiang Dong, Karl Griesbaum, Kevin J. McCullough

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

Ozonolyses of but-2-yne 1 in the presence of added carbonyl compounds 3 afford α-oxo ozonides 4. Subsequent cycloadditions between ozonides 4 and cyclohexanone oxide 6, generated in situ by ozonolysis of O-methylcyclohexanone oxime, yield in turn α-diozonides 7 into which have been incorporated the carbon skeletons of all three substrates involved. Ozonolyses of acyloxy-substituted but-2-ynes 9 yield the corresponding bicyclic α-oxo ozonides 11 which subsequently participate in analogous cycloadditions with 6 to produce the corresponding α-diozonides 12. X-Ray crystallographic analysis of the crystalline diozonide 12a shows that it has been formed exclusively by exo-addition of 6 to 11a.

Original languageEnglish (US)
Pages (from-to)1601-1604
Number of pages4
JournalJournal of the Chemical Society - Perkin Transactions 1
Issue number11
DOIs
StatePublished - Jun 7 1997

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Oximes
Alkynes
Cycloaddition
Carbonyl compounds
Oxides
Carbon
Crystalline materials
X rays
Substrates
1,2,4-trioxane

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Short path syntheses of α-diozonides by sequential ozonolyses of acetylenes and O-methyl oximes. / Dong, Yuxiang; Griesbaum, Karl; McCullough, Kevin J.

In: Journal of the Chemical Society - Perkin Transactions 1, No. 11, 07.06.1997, p. 1601-1604.

Research output: Contribution to journalArticle

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