Synthesis and properties of anti-6,15-epithia-8,13-methanobenzo[e] [14]annulene-7,14-dione, anti-5,14-epithia-7,12-methanofuro[3,4-e]-[14]annulene-5,13-diones, and their ionic species

Shengli Zuo; Shigeyasu Kuroda; Mitsunori Oda; Shin Ya Kuramoto; Yoshihiro Mizukami; Atsushi Fukuta; Yukiyasu Hirano; Teruhiko Nishikawa; Shinji Furuta; Ryuta Miyatake; Sha I. Shaheen; Takanori Kajioka; Mayumi Kyogoku

doi:10.3987/com-00-s(i)10

Synthesis and properties of anti-6,15-epithia-8,13-methanobenzo[e] [14]annulene-7,14-dione, anti-5,14-epithia-7,12-methanofuro[3,4-e]-[14]annulene-5,13-diones, and their ionic species

Shengli Zuo, Shigeyasu Kuroda^*, Mitsunori Oda, Shin Ya Kuramoto, Yoshihiro Mizukami, Atsushi Fukuta, Yukiyasu Hirano, Teruhiko Nishikawa, Shinji Furuta, Ryuta Miyatake, Sha I. Shaheen, Takanori Kajioka, Mayumi Kyogoku

^*Corresponding author for this work

Center for Environmental Conservation and Research Safety

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

2 Scopus citations

Abstract

The sulfur bridged annulene diones fused with benzene and furan were synthesized, and their ¹H and ¹³C NMR spectra in strong acid media indicated formation of dicationic species in which the positive charges localized on the carbonyl carbons, mainly due to the unfavorable p-orbital overlap.

Original language	English
Pages (from-to)	159-170
Number of pages	12
Journal	Heterocycles
Volume	54
Issue number	1
DOIs	https://doi.org/10.3987/com-00-s(i)10
State	Published - 2001/01/01

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

Access to Document

10.3987/com-00-s(i)10

Cite this

Zuo, S., Kuroda, S., Oda, M., Kuramoto, S. Y., Mizukami, Y., Fukuta, A., Hirano, Y., Nishikawa, T., Furuta, S., Miyatake, R., Shaheen, S. I., Kajioka, T., & Kyogoku, M. (2001). Synthesis and properties of anti-6,15-epithia-8,13-methanobenzo[e] [14]annulene-7,14-dione, anti-5,14-epithia-7,12-methanofuro[3,4-e]-[14]annulene-5,13-diones, and their ionic species. Heterocycles, 54(1), 159-170. https://doi.org/10.3987/com-00-s(i)10

@article{24a1574ae1214351a90e4758d8234a7a,

title = "Synthesis and properties of anti-6,15-epithia-8,13-methanobenzo[e] [14]annulene-7,14-dione, anti-5,14-epithia-7,12-methanofuro[3,4-e]-[14]annulene-5,13-diones, and their ionic species",

abstract = "The sulfur bridged annulene diones fused with benzene and furan were synthesized, and their 1H and 13C NMR spectra in strong acid media indicated formation of dicationic species in which the positive charges localized on the carbonyl carbons, mainly due to the unfavorable p-orbital overlap.",

author = "Shengli Zuo and Shigeyasu Kuroda and Mitsunori Oda and Kuramoto, {Shin Ya} and Yoshihiro Mizukami and Atsushi Fukuta and Yukiyasu Hirano and Teruhiko Nishikawa and Shinji Furuta and Ryuta Miyatake and Shaheen, {Sha I.} and Takanori Kajioka and Mayumi Kyogoku",

year = "2001",

month = jan,

day = "1",

doi = "10.3987/com-00-s(i)10",

language = "英語",

volume = "54",

pages = "159--170",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "1",

}

Zuo, S, Kuroda, S, Oda, M, Kuramoto, SY, Mizukami, Y, Fukuta, A, Hirano, Y, Nishikawa, T, Furuta, S, Miyatake, R, Shaheen, SI, Kajioka, T & Kyogoku, M 2001, 'Synthesis and properties of anti-6,15-epithia-8,13-methanobenzo[e] [14]annulene-7,14-dione, anti-5,14-epithia-7,12-methanofuro[3,4-e]-[14]annulene-5,13-diones, and their ionic species', Heterocycles, vol. 54, no. 1, pp. 159-170. https://doi.org/10.3987/com-00-s(i)10

TY - JOUR

T1 - Synthesis and properties of anti-6,15-epithia-8,13-methanobenzo[e] [14]annulene-7,14-dione, anti-5,14-epithia-7,12-methanofuro[3,4-e]-[14]annulene-5,13-diones, and their ionic species

AU - Zuo, Shengli

AU - Kuroda, Shigeyasu

AU - Oda, Mitsunori

AU - Kuramoto, Shin Ya

AU - Mizukami, Yoshihiro

AU - Fukuta, Atsushi

AU - Hirano, Yukiyasu

AU - Nishikawa, Teruhiko

AU - Furuta, Shinji

AU - Miyatake, Ryuta

AU - Shaheen, Sha I.

AU - Kajioka, Takanori

AU - Kyogoku, Mayumi

PY - 2001/1/1

Y1 - 2001/1/1

N2 - The sulfur bridged annulene diones fused with benzene and furan were synthesized, and their 1H and 13C NMR spectra in strong acid media indicated formation of dicationic species in which the positive charges localized on the carbonyl carbons, mainly due to the unfavorable p-orbital overlap.

AB - The sulfur bridged annulene diones fused with benzene and furan were synthesized, and their 1H and 13C NMR spectra in strong acid media indicated formation of dicationic species in which the positive charges localized on the carbonyl carbons, mainly due to the unfavorable p-orbital overlap.

UR - http://www.scopus.com/inward/record.url?scp=0035107547&partnerID=8YFLogxK

U2 - 10.3987/com-00-s(i)10

DO - 10.3987/com-00-s(i)10

M3 - 学術論文

AN - SCOPUS:0035107547

SN - 0385-5414

VL - 54

SP - 159

EP - 170

JO - Heterocycles

JF - Heterocycles

IS - 1

ER -

Synthesis and properties of anti-6,15-epithia-8,13-methanobenzo[e] [14]annulene-7,14-dione, anti-5,14-epithia-7,12-methanofuro[3,4-e]-[14]annulene-5,13-diones, and their ionic species

Abstract

ASJC Scopus subject areas

Access to Document

Fingerprint

Cite this