Stereospecific control of the helical orientation of indolocarbazole-pyridine hybrid foldamers by rational modification of terminal chiral appendages

Junyoung Kim; Hae Geun Jeon; Philjae Kang; Kyu Sung Jeong

doi:10.1039/c7cc03552g

Stereospecific control of the helical orientation of indolocarbazole-pyridine hybrid foldamers by rational modification of terminal chiral appendages

Junyoung Kim, Hae Geun Jeon, Philjae Kang, Kyu Sung Jeong

Department of Chemistry

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

16 Citations (Scopus)

Abstract

The helical handedness excess of an indolocarbazole-pyridine hybrid oligomer capable of folding into a stable helical structure was achieved up to 96% by rational modification of terminal chiral residues.

Original language	English
Pages (from-to)	6508-6511
Number of pages	4
Journal	Chemical Communications
Volume	53
Issue number	48
DOIs	https://doi.org/10.1039/c7cc03552g
Publication status	Published - 2017

Bibliographical note

Publisher Copyright:
© 2017 The Royal Society of Chemistry.

All Science Journal Classification (ASJC) codes

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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title = "Stereospecific control of the helical orientation of indolocarbazole-pyridine hybrid foldamers by rational modification of terminal chiral appendages",

abstract = "The helical handedness excess of an indolocarbazole-pyridine hybrid oligomer capable of folding into a stable helical structure was achieved up to 96% by rational modification of terminal chiral residues.",

author = "Junyoung Kim and Jeon, {Hae Geun} and Philjae Kang and Jeong, {Kyu Sung}",

note = "Publisher Copyright: {\textcopyright} 2017 The Royal Society of Chemistry.",

year = "2017",

doi = "10.1039/c7cc03552g",

language = "English",

volume = "53",

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journal = "Chemical Communications",

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T1 - Stereospecific control of the helical orientation of indolocarbazole-pyridine hybrid foldamers by rational modification of terminal chiral appendages

AU - Kim, Junyoung

AU - Jeon, Hae Geun

AU - Kang, Philjae

AU - Jeong, Kyu Sung

PY - 2017

Y1 - 2017

N2 - The helical handedness excess of an indolocarbazole-pyridine hybrid oligomer capable of folding into a stable helical structure was achieved up to 96% by rational modification of terminal chiral residues.

AB - The helical handedness excess of an indolocarbazole-pyridine hybrid oligomer capable of folding into a stable helical structure was achieved up to 96% by rational modification of terminal chiral residues.

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U2 - 10.1039/c7cc03552g

DO - 10.1039/c7cc03552g

M3 - Article

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AN - SCOPUS:85021705258

SN - 1359-7345

VL - 53

SP - 6508

EP - 6511

JO - Chemical Communications

JF - Chemical Communications

IS - 48

ER -

Stereospecific control of the helical orientation of indolocarbazole-pyridine hybrid foldamers by rational modification of terminal chiral appendages

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

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