Synthesis and characterization of 1,8-naphthalimide with [6]helicene skeleton

Toshitaka Kogiso; Kosuke Yamamoto; Hiroshi Suemune; Kazuteru Usui

doi:10.1039/c2ob25223f

Synthesis and characterization of 1,8-naphthalimide with [6]helicene skeleton

Toshitaka Kogiso, Kosuke Yamamoto, Hiroshi Suemune, Kazuteru Usui

Chemo-Pharmaceutical Sciences

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

16 Citations (Scopus)

Abstract

A 1,8-naphthalimide with [6]helicene derivative scaffold has been designed and synthesized. The (P)- and (M)-enantiomers of the [6]helicene derivative were resolved by HPLC on a chiral column. The single crystal of the [6]helicene derivative exhibits an intermolecular interactions of the 1,8-naphthalimide units.

Original language	English
Pages (from-to)	2934-2936
Number of pages	3
Journal	Organic and Biomolecular Chemistry
Volume	10
Issue number	15
DOIs	https://doi.org/10.1039/c2ob25223f
Publication status	Published - Apr 21 2012

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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abstract = "A 1,8-naphthalimide with [6]helicene derivative scaffold has been designed and synthesized. The (P)- and (M)-enantiomers of the [6]helicene derivative were resolved by HPLC on a chiral column. The single crystal of the [6]helicene derivative exhibits an intermolecular interactions of the 1,8-naphthalimide units.",

author = "Toshitaka Kogiso and Kosuke Yamamoto and Hiroshi Suemune and Kazuteru Usui",

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AU - Kogiso, Toshitaka

AU - Yamamoto, Kosuke

AU - Suemune, Hiroshi

AU - Usui, Kazuteru

PY - 2012/4/21

Y1 - 2012/4/21

N2 - A 1,8-naphthalimide with [6]helicene derivative scaffold has been designed and synthesized. The (P)- and (M)-enantiomers of the [6]helicene derivative were resolved by HPLC on a chiral column. The single crystal of the [6]helicene derivative exhibits an intermolecular interactions of the 1,8-naphthalimide units.

AB - A 1,8-naphthalimide with [6]helicene derivative scaffold has been designed and synthesized. The (P)- and (M)-enantiomers of the [6]helicene derivative were resolved by HPLC on a chiral column. The single crystal of the [6]helicene derivative exhibits an intermolecular interactions of the 1,8-naphthalimide units.

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Synthesis and characterization of 1,8-naphthalimide with [6]helicene skeleton

Abstract

All Science Journal Classification (ASJC) codes

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