Synthesis of 1,2,4-dioxazolidines by the ozonolysis of vinyl ethers in the presence of imines. The first [3 + 2] cycloaddition of carbonyl oxide to the carbon-nitrogen double bond

Mitsuyuki Mori; Masatomo Nojima; Shigekazu Kusabayashi; Kevin J. McCullough

doi:10.1039/C39880001550

Synthesis of 1,2,4-dioxazolidines by the ozonolysis of vinyl ethers in the presence of imines. The first [3 + 2] cycloaddition of carbonyl oxide to the carbon-nitrogen double bond

Mitsuyuki Mori, Masatomo Nojima, Shigekazu Kusabayashi, Kevin J. McCullough

School of Engineering & Physical Sciences

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

19 Citations (Scopus)

Abstract

Carbonyl oxides, derived from the ozonolysis of vinyl ethers, readily undergo [3 + 2] cycloaddition reactions with imines affording 1,2,4-dioxazolidines in good yield.

Original language	English
Pages (from-to)	1550-1552
Number of pages	3
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	23
DOIs	https://doi.org/10.1039/C39880001550
Publication status	Published - 1988

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@article{79a2c24403284fe285be710bf88bc536,

title = "Synthesis of 1,2,4-dioxazolidines by the ozonolysis of vinyl ethers in the presence of imines. The first [3 + 2] cycloaddition of carbonyl oxide to the carbon-nitrogen double bond",

abstract = "Carbonyl oxides, derived from the ozonolysis of vinyl ethers, readily undergo [3 + 2] cycloaddition reactions with imines affording 1,2,4-dioxazolidines in good yield.",

author = "Mitsuyuki Mori and Masatomo Nojima and Shigekazu Kusabayashi and McCullough, {Kevin J.}",

year = "1988",

doi = "10.1039/C39880001550",

language = "English",

pages = "1550--1552",

journal = "Journal of the Chemical Society, Chemical Communications",

issn = "0022-4936",

publisher = "Chemical Society",

number = "23",

}

Synthesis of 1,2,4-dioxazolidines by the ozonolysis of vinyl ethers in the presence of imines. The first [3 + 2] cycloaddition of carbonyl oxide to the carbon-nitrogen double bond. / Mori, Mitsuyuki; Nojima, Masatomo; Kusabayashi, Shigekazu et al.
In: Journal of the Chemical Society, Chemical Communications, No. 23, 1988, p. 1550-1552.

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

TY - JOUR

T1 - Synthesis of 1,2,4-dioxazolidines by the ozonolysis of vinyl ethers in the presence of imines. The first [3 + 2] cycloaddition of carbonyl oxide to the carbon-nitrogen double bond

AU - Mori, Mitsuyuki

AU - Nojima, Masatomo

AU - Kusabayashi, Shigekazu

AU - McCullough, Kevin J.

PY - 1988

Y1 - 1988

N2 - Carbonyl oxides, derived from the ozonolysis of vinyl ethers, readily undergo [3 + 2] cycloaddition reactions with imines affording 1,2,4-dioxazolidines in good yield.

AB - Carbonyl oxides, derived from the ozonolysis of vinyl ethers, readily undergo [3 + 2] cycloaddition reactions with imines affording 1,2,4-dioxazolidines in good yield.

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U2 - 10.1039/C39880001550

DO - 10.1039/C39880001550

M3 - Article

SN - 0022-4936

SP - 1550

EP - 1552

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 23

ER -

Synthesis of 1,2,4-dioxazolidines by the ozonolysis of vinyl ethers in the presence of imines. The first [3 + 2] cycloaddition of carbonyl oxide to the carbon-nitrogen double bond

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