Catalytic asymmetric iodocarbocyclization reaction

Tadashi Inoue; Osamu Kitagawa; Orie Ochiai; Motoo Shiro; Takeo Taguchi

doi:10.1016/0040-4039(95)02021-G

Catalytic asymmetric iodocarbocyclization reaction

Tadashi Inoue, Osamu Kitagawa, Orie Ochiai, Motoo Shiro, Takeo Taguchi

研究成果: Article

42 引用（Scopus）

抜粋

The iodocarbocyclization reactions of 4-pentenylmalonate derivatives using 20 mol% of the chiral titanium complex in the presence of 12 end 2,6-dimethoxypyridine proceeded with high enantioselectivity to give good yields of cyclopentane derivatives. The origin of enantioselectivity in the present reaction is discussed on the basis of X-ray crystal structural data of the chiral titanium complex from acetylacetone, chiral dial and Ti(IV).

元の言語	English
ページ（範囲）	9333-9336
ページ数	4
ジャーナル	Tetrahedron Letters
巻	36
発行部数	51
DOI	https://doi.org/10.1016/0040-4039(95)02021-G
出版物ステータス	Published - 1995 12 18
外部発表	Yes

フィンガープリント

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

これを引用

Inoue, T., Kitagawa, O., Ochiai, O., Shiro, M., & Taguchi, T. (1995). Catalytic asymmetric iodocarbocyclization reaction. Tetrahedron Letters, 36(51), 9333-9336. https://doi.org/10.1016/0040-4039(95)02021-G

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author = "Tadashi Inoue and Osamu Kitagawa and Orie Ochiai and Motoo Shiro and Takeo Taguchi",

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T1 - Catalytic asymmetric iodocarbocyclization reaction

AU - Inoue, Tadashi

AU - Kitagawa, Osamu

AU - Ochiai, Orie

AU - Shiro, Motoo

AU - Taguchi, Takeo

PY - 1995/12/18

Y1 - 1995/12/18

N2 - The iodocarbocyclization reactions of 4-pentenylmalonate derivatives using 20 mol% of the chiral titanium complex in the presence of 12 end 2,6-dimethoxypyridine proceeded with high enantioselectivity to give good yields of cyclopentane derivatives. The origin of enantioselectivity in the present reaction is discussed on the basis of X-ray crystal structural data of the chiral titanium complex from acetylacetone, chiral dial and Ti(IV).

AB - The iodocarbocyclization reactions of 4-pentenylmalonate derivatives using 20 mol% of the chiral titanium complex in the presence of 12 end 2,6-dimethoxypyridine proceeded with high enantioselectivity to give good yields of cyclopentane derivatives. The origin of enantioselectivity in the present reaction is discussed on the basis of X-ray crystal structural data of the chiral titanium complex from acetylacetone, chiral dial and Ti(IV).

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U2 - 10.1016/0040-4039(95)02021-G

DO - 10.1016/0040-4039(95)02021-G

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VL - 36

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 51

ER -

文献にアクセス

10.1016/0040-4039(95)02021-G