An efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines

Hui Young Ku; Junyang Jung; Soo Hyun Kim; Hee Yeon Kim; Kyo Han Ahn; Sung Gon Kim

doi:10.1016/j.tetasy.2006.03.031

An efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines

Hui Young Ku
, Junyang Jung
, Soo Hyun Kim
, Hee Yeon Kim
, Kyo Han Ahn
, Sung Gon Kim

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

14 Citations (Scopus)

Abstract

A quick route to enantiomerically pure unnatural aryl glycinols and aryl glycines has been established based on an asymmetric azidation reaction using a chiral benzosultam auxiliary. The synthesis of aryl glycinols involves three steps starting from arylacetic acids, and the chiral auxiliary can be readily recovered.

Original language	English
Pages (from-to)	1111-1115
Number of pages	5
Journal	Tetrahedron Asymmetry
Volume	17
Issue number	7
DOIs	https://doi.org/10.1016/j.tetasy.2006.03.031
Publication status	Published - 3 Apr 2006

Bibliographical note

Funding Information:
This work was supported by the Korea Science & Engineering Foundation (Basic Research Program, Grant No. R02-2002-000-00103-0) and the Center for Integrated Molecular Systems. We are also grateful to the Ministry of Commerce, Industry, and Energy (TS-052-03) for the financial support.

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10.1016/j.tetasy.2006.03.031

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abstract = "A quick route to enantiomerically pure unnatural aryl glycinols and aryl glycines has been established based on an asymmetric azidation reaction using a chiral benzosultam auxiliary. The synthesis of aryl glycinols involves three steps starting from arylacetic acids, and the chiral auxiliary can be readily recovered.",

author = "Ku, \{Hui Young\} and Junyang Jung and Kim, \{Soo Hyun\} and Kim, \{Hee Yeon\} and Ahn, \{Kyo Han\} and Kim, \{Sung Gon\}",

note = "Funding Information: This work was supported by the Korea Science \& Engineering Foundation (Basic Research Program, Grant No. R02-2002-000-00103-0) and the Center for Integrated Molecular Systems. We are also grateful to the Ministry of Commerce, Industry, and Energy (TS-052-03) for the financial support. ",

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doi = "10.1016/j.tetasy.2006.03.031",

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T1 - An efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines

AU - Ku, Hui Young

AU - Jung, Junyang

AU - Kim, Soo Hyun

AU - Kim, Hee Yeon

AU - Ahn, Kyo Han

AU - Kim, Sung Gon

N1 - Funding Information: This work was supported by the Korea Science & Engineering Foundation (Basic Research Program, Grant No. R02-2002-000-00103-0) and the Center for Integrated Molecular Systems. We are also grateful to the Ministry of Commerce, Industry, and Energy (TS-052-03) for the financial support.

PY - 2006/4/3

Y1 - 2006/4/3

N2 - A quick route to enantiomerically pure unnatural aryl glycinols and aryl glycines has been established based on an asymmetric azidation reaction using a chiral benzosultam auxiliary. The synthesis of aryl glycinols involves three steps starting from arylacetic acids, and the chiral auxiliary can be readily recovered.

AB - A quick route to enantiomerically pure unnatural aryl glycinols and aryl glycines has been established based on an asymmetric azidation reaction using a chiral benzosultam auxiliary. The synthesis of aryl glycinols involves three steps starting from arylacetic acids, and the chiral auxiliary can be readily recovered.

UR - https://www.scopus.com/pages/publications/33646526018

U2 - 10.1016/j.tetasy.2006.03.031

DO - 10.1016/j.tetasy.2006.03.031

M3 - Article

AN - SCOPUS:33646526018

SN - 0957-4166

VL - 17

SP - 1111

EP - 1115

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 7

ER -

An efficient synthesis of enantiomerically pure unnatural aryl glycinols and aryl glycines

Abstract

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