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

21 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

Access to Document

10.1021/ol006478p

Cite this

@article{b6f5356d7bb54fb3a41db1db59aa5c65,

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",

month = oct,

day = "19",

doi = "10.1021/ol006478p",

language = "English (US)",

volume = "2",

pages = "3377--3379",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "21",

}

TY - JOUR

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

N2 - (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.

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.

UR - http://www.scopus.com/inward/record.url?scp=0034687180&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034687180&partnerID=8YFLogxK

U2 - 10.1021/ol006478p

DO - 10.1021/ol006478p

M3 - Article

C2 - 11029215

AN - SCOPUS:0034687180

SN - 1523-7060

VL - 2

SP - 3377

EP - 3379

JO - Organic Letters

JF - Organic Letters

IS - 21

ER -

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

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this