Synthesis of methyl epi-anhydroquinate utilizing [2,3]-sigmatropic rearrangement of iodosoalkene

Sho Inomata; Minoru Ueda; Takeshi Sugai; Mitsuru Shoji

doi:10.1246/cl.130612

Synthesis of methyl epi-anhydroquinate utilizing [2,3]-sigmatropic rearrangement of iodosoalkene

Sho Inomata
, Minoru Ueda
, Takeshi Sugai
, Mitsuru Shoji

薬科学科

研究成果: Article › 査読

2 被引用数 (Scopus)

抄録

Sigmatropic rearrangement has been utilized for stereoselective syntheses of structurally complicated natural products because of its high stereoselectivity and reactivity. Quinic acid (1) and its epimer 2 are versatile building blocks for the preparation of various bioactive compounds. We report the synthesis of methyl epi-anhydroquinate 3 via the [2,3]-sigmatropic rearrangement of iodosoalkene.

本文言語	English
ページ（範囲）	1273-1275
ページ数	3
ジャーナル	Chemistry Letters
巻	42
号	10
DOI	https://doi.org/10.1246/cl.130612
出版ステータス	Published - 2013

ASJC Scopus subject areas

化学一般

文献へのアクセス

10.1246/cl.130612

他のファイルとリンク

引用スタイル

@article{956697d7f41d46e5a088bb40faa5387e,

title = "Synthesis of methyl epi-anhydroquinate utilizing [2,3]-sigmatropic rearrangement of iodosoalkene",

abstract = "Sigmatropic rearrangement has been utilized for stereoselective syntheses of structurally complicated natural products because of its high stereoselectivity and reactivity. Quinic acid (1) and its epimer 2 are versatile building blocks for the preparation of various bioactive compounds. We report the synthesis of methyl epi-anhydroquinate 3 via the [2,3]-sigmatropic rearrangement of iodosoalkene.",

author = "Sho Inomata and Minoru Ueda and Takeshi Sugai and Mitsuru Shoji",

year = "2013",

doi = "10.1246/cl.130612",

language = "English",

volume = "42",

pages = "1273--1275",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Oxford University Press",

number = "10",

}

TY - JOUR

T1 - Synthesis of methyl epi-anhydroquinate utilizing [2,3]-sigmatropic rearrangement of iodosoalkene

AU - Inomata, Sho

AU - Ueda, Minoru

AU - Sugai, Takeshi

AU - Shoji, Mitsuru

PY - 2013

Y1 - 2013

N2 - Sigmatropic rearrangement has been utilized for stereoselective syntheses of structurally complicated natural products because of its high stereoselectivity and reactivity. Quinic acid (1) and its epimer 2 are versatile building blocks for the preparation of various bioactive compounds. We report the synthesis of methyl epi-anhydroquinate 3 via the [2,3]-sigmatropic rearrangement of iodosoalkene.

AB - Sigmatropic rearrangement has been utilized for stereoselective syntheses of structurally complicated natural products because of its high stereoselectivity and reactivity. Quinic acid (1) and its epimer 2 are versatile building blocks for the preparation of various bioactive compounds. We report the synthesis of methyl epi-anhydroquinate 3 via the [2,3]-sigmatropic rearrangement of iodosoalkene.

UR - https://www.scopus.com/pages/publications/84885353837

UR - https://www.scopus.com/pages/publications/84885353837#tab=citedBy

U2 - 10.1246/cl.130612

DO - 10.1246/cl.130612

M3 - Article

AN - SCOPUS:84885353837

SN - 0366-7022

VL - 42

SP - 1273

EP - 1275

JO - Chemistry Letters

JF - Chemistry Letters

IS - 10

ER -

Synthesis of methyl epi-anhydroquinate utilizing [2,3]-sigmatropic rearrangement of iodosoalkene

抄録

ASJC Scopus subject areas

文献へのアクセス

他のファイルとリンク

フィンガープリント

引用スタイル