2007年7月
Synthesis of novel axially chiral cyclic benzopolysulfides
TETRAHEDRON LETTERS
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- 巻
- 48
- 号
- 29
- 開始ページ
- 4991
- 終了ページ
- 4994
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1016/j.tetlet.2007.05.117
- 出版者・発行元
- PERGAMON-ELSEVIER SCIENCE LTD
Novel axially chiral benzopentathiepins were synthesized by sulfurization of dithiastannole. Naphthyl moiety was introduced near the pentathiepin ring by Suzuki-Miyaura cross-coupling reaction. Pentathiepins were found as diastereomeric mixture. Rotational energy barrier for C-C bond was estimated by theoretical calculation. Energy barrier for the inversion of pentathiepin ring was experimentally determined by variable temperature H-1 NMR. (C) 2007 Published by Elsevier Ltd.
- リンク情報
- ID情報
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- DOI : 10.1016/j.tetlet.2007.05.117
- ISSN : 0040-4039
- CiNii Articles ID : 80018476645
- Web of Science ID : WOS:000247995900007