Transformation of 1-alkyl-substituted indene ozonides and the corresponding solvent-derived ozonolysis products to tricyclic peroxides: Isolation and characterization of novel hexoxecane derivatives

Yoshihiro Ushigoe; Shin Ichi Kawamura; Koichi Teshima; Masatomo Nojima; Kevin J. McCullough

doi:10.1016/0040-4039(96)00201-8

Transformation of 1-alkyl-substituted indene ozonides and the corresponding solvent-derived ozonolysis products to tricyclic peroxides: Isolation and characterization of novel hexoxecane derivatives

Yoshihiro Ushigoe, Shin Ichi Kawamura, Koichi Teshima, Masatomo Nojima, Kevin J. McCullough

School of Engineering & Physical Sciences

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

5 Citations (Scopus)

Abstract

Acidolysis of 1-alkyl-substituted indene ozonides 3a,c,d or the corresponding solvent-derived ozonolysis products 5a-d gave the hexoxecane derivatives 4a-d. The structure of the compound 4a was unambiguously established by the X-ray crystallographic analysis, which demonstrated that the hexoxecane 4a is derived from dimerization of molecules of 3a or 5a of the same configuration.

Original language	English
Pages (from-to)	2093-2096
Number of pages	4
Journal	Tetrahedron Letters
Volume	37
Issue number	12
DOIs	https://doi.org/10.1016/0040-4039(96)00201-8
Publication status	Published - 18 Mar 1996

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10.1016/0040-4039(96)00201-8

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title = "Transformation of 1-alkyl-substituted indene ozonides and the corresponding solvent-derived ozonolysis products to tricyclic peroxides: Isolation and characterization of novel hexoxecane derivatives",

abstract = "Acidolysis of 1-alkyl-substituted indene ozonides 3a,c,d or the corresponding solvent-derived ozonolysis products 5a-d gave the hexoxecane derivatives 4a-d. The structure of the compound 4a was unambiguously established by the X-ray crystallographic analysis, which demonstrated that the hexoxecane 4a is derived from dimerization of molecules of 3a or 5a of the same configuration.",

author = "Yoshihiro Ushigoe and Kawamura, {Shin Ichi} and Koichi Teshima and Masatomo Nojima and McCullough, {Kevin J.}",

year = "1996",

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doi = "10.1016/0040-4039(96)00201-8",

language = "English",

volume = "37",

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journal = "Tetrahedron Letters",

publisher = "Elsevier",

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Ushigoe, Y, Kawamura, SI, Teshima, K, Nojima, M & McCullough, KJ 1996, 'Transformation of 1-alkyl-substituted indene ozonides and the corresponding solvent-derived ozonolysis products to tricyclic peroxides: Isolation and characterization of novel hexoxecane derivatives', Tetrahedron Letters, vol. 37, no. 12, pp. 2093-2096. https://doi.org/10.1016/0040-4039(96)00201-8

Transformation of 1-alkyl-substituted indene ozonides and the corresponding solvent-derived ozonolysis products to tricyclic peroxides: Isolation and characterization of novel hexoxecane derivatives. / Ushigoe, Yoshihiro; Kawamura, Shin Ichi; Teshima, Koichi et al.
In: Tetrahedron Letters, Vol. 37, No. 12, 18.03.1996, p. 2093-2096.

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

TY - JOUR

T1 - Transformation of 1-alkyl-substituted indene ozonides and the corresponding solvent-derived ozonolysis products to tricyclic peroxides

T2 - Isolation and characterization of novel hexoxecane derivatives

AU - Ushigoe, Yoshihiro

AU - Kawamura, Shin Ichi

AU - Teshima, Koichi

AU - Nojima, Masatomo

AU - McCullough, Kevin J.

PY - 1996/3/18

Y1 - 1996/3/18

N2 - Acidolysis of 1-alkyl-substituted indene ozonides 3a,c,d or the corresponding solvent-derived ozonolysis products 5a-d gave the hexoxecane derivatives 4a-d. The structure of the compound 4a was unambiguously established by the X-ray crystallographic analysis, which demonstrated that the hexoxecane 4a is derived from dimerization of molecules of 3a or 5a of the same configuration.

AB - Acidolysis of 1-alkyl-substituted indene ozonides 3a,c,d or the corresponding solvent-derived ozonolysis products 5a-d gave the hexoxecane derivatives 4a-d. The structure of the compound 4a was unambiguously established by the X-ray crystallographic analysis, which demonstrated that the hexoxecane 4a is derived from dimerization of molecules of 3a or 5a of the same configuration.

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U2 - 10.1016/0040-4039(96)00201-8

DO - 10.1016/0040-4039(96)00201-8

M3 - Article

VL - 37

SP - 2093

EP - 2096

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 12

ER -

Transformation of 1-alkyl-substituted indene ozonides and the corresponding solvent-derived ozonolysis products to tricyclic peroxides: Isolation and characterization of novel hexoxecane derivatives

Abstract

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