Ozonolysis in the presence of Lewis acids: Directed addition to carbonyl oxides

Patrick H. Dussault; Joseph M. Raible

doi:10.1021/ol006478p

Ozonolysis in the presence of Lewis acids: Directed addition to carbonyl oxides

Patrick H. Dussault, Joseph M. Raible

Chemistry

Research output: Contribution to journal › Article › peer-review

19 Scopus citations

Abstract

(matrix presented) The presence of Lewis acids strongly influences the distribution of products from alkene ozonolysis. Delivery of alkoxide and phenoxide ligands to a coordinated carbonyl oxide affords hydroperoxyacetals under aprotic conditions.

Original language	English (US)
Pages (from-to)	3377-3379
Number of pages	3
Journal	Organic Letters
Volume	2
Issue number	21
DOIs	https://doi.org/10.1021/ol006478p
State	Published - Oct 19 2000

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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title = "Ozonolysis in the presence of Lewis acids: Directed addition to carbonyl oxides",

abstract = "(matrix presented) The presence of Lewis acids strongly influences the distribution of products from alkene ozonolysis. Delivery of alkoxide and phenoxide ligands to a coordinated carbonyl oxide affords hydroperoxyacetals under aprotic conditions.",

author = "Dussault, {Patrick H.} and Raible, {Joseph M.}",

year = "2000",

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doi = "10.1021/ol006478p",

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T1 - Ozonolysis in the presence of Lewis acids

T2 - Directed addition to carbonyl oxides

AU - Dussault, Patrick H.

AU - Raible, Joseph M.

PY - 2000/10/19

Y1 - 2000/10/19

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AB - (matrix presented) The presence of Lewis acids strongly influences the distribution of products from alkene ozonolysis. Delivery of alkoxide and phenoxide ligands to a coordinated carbonyl oxide affords hydroperoxyacetals under aprotic conditions.

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JO - Organic Letters

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ER -

Ozonolysis in the presence of Lewis acids: Directed addition to carbonyl oxides

Abstract

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