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 › peer-review

26 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 Mar
Externally published	Yes

ASJC Scopus subject areas

Catalysis
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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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",

year = "1995",

month = mar,

doi = "10.1016/0957-4166(95)00063-U",

language = "English",

volume = "6",

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journal = "Tetrahedron Asymmetry",

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T1 - Diastereoselective iodocarbocyclization reaction of 8-phenylmenthyl allylmalonate

T2 - An efficient preparation of a synthetic intermediate of cyclopropane amino acids

AU - Inoue, Tadashi

AU - Kitagawa, Osamu

AU - Ochiai, Orie

AU - Taguchi, Takeo

PY - 1995/3

Y1 - 1995/3

N2 - The iodocarbocyclization of allylmalonate using (-)-8-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give the iodomethylcyclopropane dicarboxylic ester in good yield.

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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U2 - 10.1016/0957-4166(95)00063-U

DO - 10.1016/0957-4166(95)00063-U

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VL - 6

SP - 691

EP - 692

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

SN - 0957-4166

IS - 3

ER -

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

Abstract

ASJC Scopus subject areas

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