Diastereoselective 1,3-dipolar cycloaddition of ynolates with chiral nitrones

Mitsuru Shindo; Kotaro Itoh; Keiko Ohtsuki; Chinatsu Tsuchiya; Kozo Shishido

doi:10.1055/s-2003-40189

Diastereoselective 1,3-dipolar cycloaddition of ynolates with chiral nitrones

Mitsuru Shindo, Kotaro Itoh, Keiko Ohtsuki, Chinatsu Tsuchiya, Kozo Shishido

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

17 Citations (Scopus)

Abstract

Asymmetric inverse electron-demand 1,3-dipolar cycloaddition of ynolates with chiral nitrones produced 5-isoxazolidinones with good diastereoselectivity. These products were easily converted into optically pure β-amino acids and chiral γ-butyrolactones.

Original language	English
Pages (from-to)	1441-1445
Number of pages	5
Journal	Synthesis
Issue number	9
DOIs	https://doi.org/10.1055/s-2003-40189
Publication status	Published - 2003
Externally published	Yes

All Science Journal Classification (ASJC) codes

Catalysis
Organic Chemistry

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10.1055/s-2003-40189

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title = "Diastereoselective 1,3-dipolar cycloaddition of ynolates with chiral nitrones",

abstract = "Asymmetric inverse electron-demand 1,3-dipolar cycloaddition of ynolates with chiral nitrones produced 5-isoxazolidinones with good diastereoselectivity. These products were easily converted into optically pure β-amino acids and chiral γ-butyrolactones.",

author = "Mitsuru Shindo and Kotaro Itoh and Keiko Ohtsuki and Chinatsu Tsuchiya and Kozo Shishido",

year = "2003",

doi = "10.1055/s-2003-40189",

language = "English",

pages = "1441--1445",

journal = "Synthesis",

issn = "0039-7881",

publisher = "Georg Thieme Verlag",

number = "9",

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T1 - Diastereoselective 1,3-dipolar cycloaddition of ynolates with chiral nitrones

AU - Shindo, Mitsuru

AU - Itoh, Kotaro

AU - Ohtsuki, Keiko

AU - Tsuchiya, Chinatsu

AU - Shishido, Kozo

PY - 2003

Y1 - 2003

N2 - Asymmetric inverse electron-demand 1,3-dipolar cycloaddition of ynolates with chiral nitrones produced 5-isoxazolidinones with good diastereoselectivity. These products were easily converted into optically pure β-amino acids and chiral γ-butyrolactones.

AB - Asymmetric inverse electron-demand 1,3-dipolar cycloaddition of ynolates with chiral nitrones produced 5-isoxazolidinones with good diastereoselectivity. These products were easily converted into optically pure β-amino acids and chiral γ-butyrolactones.

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U2 - 10.1055/s-2003-40189

DO - 10.1055/s-2003-40189

M3 - Article

AN - SCOPUS:0037560998

SN - 0039-7881

SP - 1441

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JO - Synthesis

JF - Synthesis

IS - 9

ER -

Diastereoselective 1,3-dipolar cycloaddition of ynolates with chiral nitrones

Abstract

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