Studies toward the total synthesis of nakiterpiosin: construction of the CDE ring system by a transannular Diels-Alder strategy

Tomonori Ito; Masahiro Ito; Hirokazu Arimoto; Hiroyoshi Takamura; Daisuke Uemura

doi:10.1016/j.tetlet.2007.05.174

Studies toward the total synthesis of nakiterpiosin: construction of the CDE ring system by a transannular Diels-Alder strategy

Tomonori Ito, Masahiro Ito, Hirokazu Arimoto, Hiroyoshi Takamura, Daisuke Uemura

LIF - Molecular and Chemical Life Science

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

20 Citations (Scopus)

Abstract

The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). Tetracyclic compound 25 may be a key intermediate in the total synthesis of 1.

Original language	English
Pages (from-to)	5465-5469
Number of pages	5
Journal	Tetrahedron Letters
Volume	48
Issue number	31
DOIs	https://doi.org/10.1016/j.tetlet.2007.05.174
Publication status	Published - 2007 Jul 30

Keywords

Nakiterpiosin
Synthetic study
Transannular Diels-Alder reaction

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2007.05.174

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title = "Studies toward the total synthesis of nakiterpiosin: construction of the CDE ring system by a transannular Diels-Alder strategy",

abstract = "The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). Tetracyclic compound 25 may be a key intermediate in the total synthesis of 1.",

keywords = "Nakiterpiosin, Synthetic study, Transannular Diels-Alder reaction",

author = "Tomonori Ito and Masahiro Ito and Hirokazu Arimoto and Hiroyoshi Takamura and Daisuke Uemura",

note = "Funding Information: This work was supported in part by a Grant-in-Aid for Creative Scientific Research (16GS0206) from the Ministry of Education, Culture, Sports, Science and Technology, Japan.",

year = "2007",

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doi = "10.1016/j.tetlet.2007.05.174",

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T2 - construction of the CDE ring system by a transannular Diels-Alder strategy

AU - Ito, Tomonori

AU - Ito, Masahiro

AU - Arimoto, Hirokazu

AU - Takamura, Hiroyoshi

AU - Uemura, Daisuke

N1 - Funding Information: This work was supported in part by a Grant-in-Aid for Creative Scientific Research (16GS0206) from the Ministry of Education, Culture, Sports, Science and Technology, Japan.

PY - 2007/7/30

Y1 - 2007/7/30

N2 - The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). Tetracyclic compound 25 may be a key intermediate in the total synthesis of 1.

AB - The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). Tetracyclic compound 25 may be a key intermediate in the total synthesis of 1.

KW - Nakiterpiosin

KW - Synthetic study

KW - Transannular Diels-Alder reaction

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M3 - Article

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JF - Tetrahedron Letters

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Studies toward the total synthesis of nakiterpiosin: construction of the CDE ring system by a transannular Diels-Alder strategy

Abstract

Keywords

ASJC Scopus subject areas

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