Convergent Synthesis of a Trans-fused 6-7-6 Tricyclic Ether System Based on a Ring-closing Metathesis Reaction

Tohru Oishi; Yoko Nagumo; Masahiro Hirama

doi:10.1055/s-1997-969

Convergent Synthesis of a Trans-fused 6-7-6 Tricyclic Ether System Based on a Ring-closing Metathesis Reaction

Tohru Oishi, Yoko Nagumo, Masahiro Hirama

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

52 被引用数 (Scopus)

抄録

Synthesis of a trans-fused 6-7-6 tricyclic ether system was achieved via stereoselective acetal formation, reductive cleavage of the acetal, and a ring-closing metathesis reaction.

本文言語	英語
ページ（範囲）	980-982
ページ数	3
ジャーナル	Synlett
巻	1997
号	8
DOI	https://doi.org/10.1055/s-1997-969
出版ステータス	出版済み - 1月 1 1997
外部発表	はい

!!!All Science Journal Classification (ASJC) codes

有機化学

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10.1055/s-1997-969

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title = "Convergent Synthesis of a Trans-fused 6-7-6 Tricyclic Ether System Based on a Ring-closing Metathesis Reaction",

abstract = "Synthesis of a trans-fused 6-7-6 tricyclic ether system was achieved via stereoselective acetal formation, reductive cleavage of the acetal, and a ring-closing metathesis reaction.",

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AB - Synthesis of a trans-fused 6-7-6 tricyclic ether system was achieved via stereoselective acetal formation, reductive cleavage of the acetal, and a ring-closing metathesis reaction.

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Convergent Synthesis of a Trans-fused 6-7-6 Tricyclic Ether System Based on a Ring-closing Metathesis Reaction

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!!!All Science Journal Classification (ASJC) codes

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