Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids

Tadashi Inoue; Osamu Kitagawa; Orie Ochiai; Takeo Taguchi

doi:10.1016/0957-4166(95)00063-U

Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids

Tadashi Inoue, Osamu Kitagawa, Orie Ochiai, Takeo Taguchi

Research output: Contribution to journal › Article

25 Citations (Scopus)

Abstract

The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.

Original language	English
Pages (from-to)	691-692
Number of pages	2
Journal	Tetrahedron: Asymmetry
Volume	6
Issue number	3
DOIs	https://doi.org/10.1016/0957-4166(95)00063-U
Publication status	Published - 1995
Externally published	Yes

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ASJC Scopus subject areas

Catalysis
Inorganic Chemistry
Organic Chemistry
Physical and Theoretical Chemistry
Materials Chemistry
Drug Discovery

Cite this

Inoue, T., Kitagawa, O., Ochiai, O., & Taguchi, T. (1995). Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids. Tetrahedron: Asymmetry, 6(3), 691-692. https://doi.org/10.1016/0957-4166(95)00063-U

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title = "Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate: An efficient preparation of a synthetic intermediate of cyclopropane amino acids",

abstract = "The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.",

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

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AU - Kitagawa, Osamu

AU - Ochiai, Orie

AU - Taguchi, Takeo

PY - 1995

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AB - The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.

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Access to Document

10.1016/0957-4166(95)00063-U