New C2-symmetric chiral ketones for catalytic asymmetric epoxidation of unfunctionalized olefins

Choong Eui Song; Yang Hee Kim; Kyo Chul Lee; Sang Gi Lee; Byung Woo Jin

doi:10.1016/S0957-4166(97)00352-2

New C₂-symmetric chiral ketones for catalytic asymmetric epoxidation of unfunctionalized olefins

Choong Eui Song
, Yang Hee Kim
, Kyo Chul Lee
, Sang Gi Lee
, Byung Woo Jin

Department of Chemistry & Nanoscience

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

83 Scopus citations

Abstract

Using new C₂-symmetric chiral ketones 4 and 6 as precursors for chiral dioxiranes generated in situ, the asymmetric epoxidation of olefins has been achieved in moderate ee.

Original language	English
Pages (from-to)	2921-2926
Number of pages	6
Journal	Tetrahedron Asymmetry
Volume	8
Issue number	17
DOIs	https://doi.org/10.1016/S0957-4166(97)00352-2
State	Published - 11 Sep 1997

Bibliographical note

Funding Information:
This research was supported by a grant (1-2El4003-24-0) from the Ministry of Science and Technology in Korea. We also thank Dr Kwan Mook Kim for X-ray crystallographic structure determination.

Access to Document

10.1016/S0957-4166(97)00352-2

Cite this

@article{c19f89f05cc74f1ebd0f704ffe755151,

title = "New C2-symmetric chiral ketones for catalytic asymmetric epoxidation of unfunctionalized olefins",

abstract = "Using new C2-symmetric chiral ketones 4 and 6 as precursors for chiral dioxiranes generated in situ, the asymmetric epoxidation of olefins has been achieved in moderate ee.",

author = "Song, \{Choong Eui\} and Kim, \{Yang Hee\} and Lee, \{Kyo Chul\} and Lee, \{Sang Gi\} and Jin, \{Byung Woo\}",

note = "Funding Information: This research was supported by a grant (1-2El4003-24-0) from the Ministry of Science and Technology in Korea. We also thank Dr Kwan Mook Kim for X-ray crystallographic structure determination.",

year = "1997",

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pages = "2921--2926",

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T1 - New C2-symmetric chiral ketones for catalytic asymmetric epoxidation of unfunctionalized olefins

AU - Song, Choong Eui

AU - Kim, Yang Hee

AU - Lee, Kyo Chul

AU - Lee, Sang Gi

AU - Jin, Byung Woo

N1 - Funding Information: This research was supported by a grant (1-2El4003-24-0) from the Ministry of Science and Technology in Korea. We also thank Dr Kwan Mook Kim for X-ray crystallographic structure determination.

PY - 1997/9/11

Y1 - 1997/9/11

N2 - Using new C2-symmetric chiral ketones 4 and 6 as precursors for chiral dioxiranes generated in situ, the asymmetric epoxidation of olefins has been achieved in moderate ee.

AB - Using new C2-symmetric chiral ketones 4 and 6 as precursors for chiral dioxiranes generated in situ, the asymmetric epoxidation of olefins has been achieved in moderate ee.

UR - https://www.scopus.com/pages/publications/0030865630

U2 - 10.1016/S0957-4166(97)00352-2

DO - 10.1016/S0957-4166(97)00352-2

M3 - Article

AN - SCOPUS:0030865630

SN - 0957-4166

VL - 8

SP - 2921

EP - 2926

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 17