Stereoselective multimodal transformations of planar chiral 9-membered diallylic amides

Katsuhiko Tomooka; Masaki Suzuki; Maki Shimada; Runyan Ni; Kazuhiro Uehara

doi:10.1021/ol202009x

Stereoselective multimodal transformations of planar chiral 9-membered diallylic amides

Katsuhiko Tomooka
, Masaki Suzuki
, Maki Shimada
, Runyan Ni
, Kazuhiro Uehara

分子集積化学部門

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

19 被引用数 (Scopus)

抄録

Intermolecular reactions of planar chiral 9-membered diallylic amides provide a variety of bicyclic compounds with central chiralities in a stereospecific fashion with high group selectivity. Lewis-acid-promoted intramolecular reactions of the obtained bicyclic compounds provide transannular products in a stereospecific fashion. Furthermore, a direct transannular reaction of diallylic amide involving sequential intermolecular-intramolecular reactions has been developed.

本文言語	英語
ページ（範囲）	4926-4929
ページ数	4
ジャーナル	Organic letters
巻	13
号	18
DOI	https://doi.org/10.1021/ol202009x
出版ステータス	出版済み - 9月 16 2011

!!!All Science Journal Classification (ASJC) codes

生化学
物理化学および理論化学
有機化学

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10.1021/ol202009x

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title = "Stereoselective multimodal transformations of planar chiral 9-membered diallylic amides",

abstract = "Intermolecular reactions of planar chiral 9-membered diallylic amides provide a variety of bicyclic compounds with central chiralities in a stereospecific fashion with high group selectivity. Lewis-acid-promoted intramolecular reactions of the obtained bicyclic compounds provide transannular products in a stereospecific fashion. Furthermore, a direct transannular reaction of diallylic amide involving sequential intermolecular-intramolecular reactions has been developed.",

author = "Katsuhiko Tomooka and Masaki Suzuki and Maki Shimada and Runyan Ni and Kazuhiro Uehara",

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T1 - Stereoselective multimodal transformations of planar chiral 9-membered diallylic amides

AU - Tomooka, Katsuhiko

AU - Suzuki, Masaki

AU - Shimada, Maki

AU - Ni, Runyan

AU - Uehara, Kazuhiro

PY - 2011/9/16

Y1 - 2011/9/16

N2 - Intermolecular reactions of planar chiral 9-membered diallylic amides provide a variety of bicyclic compounds with central chiralities in a stereospecific fashion with high group selectivity. Lewis-acid-promoted intramolecular reactions of the obtained bicyclic compounds provide transannular products in a stereospecific fashion. Furthermore, a direct transannular reaction of diallylic amide involving sequential intermolecular-intramolecular reactions has been developed.

AB - Intermolecular reactions of planar chiral 9-membered diallylic amides provide a variety of bicyclic compounds with central chiralities in a stereospecific fashion with high group selectivity. Lewis-acid-promoted intramolecular reactions of the obtained bicyclic compounds provide transannular products in a stereospecific fashion. Furthermore, a direct transannular reaction of diallylic amide involving sequential intermolecular-intramolecular reactions has been developed.

UR - https://www.scopus.com/pages/publications/80052778187

UR - https://www.scopus.com/pages/publications/80052778187#tab=citedBy

U2 - 10.1021/ol202009x

DO - 10.1021/ol202009x

M3 - Article

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JO - Organic letters

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ER -

Stereoselective multimodal transformations of planar chiral 9-membered diallylic amides

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!!!All Science Journal Classification (ASJC) codes

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