Exploration for large-scale stereoselective synthesis of unusual amino acids by using 4-phenyloxazolidin-2-one as a new chiral resolution reagent

Guigen Li; Dinesh Patel; Victor J. Hruby

doi:10.1039/p19940003057

Exploration for large-scale stereoselective synthesis of unusual amino acids by using 4-phenyloxazolidin-2-one as a new chiral resolution reagent

Guigen Li, Dinesh Patel, Victor J. Hruby

Chemistry and Biochemistry

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

24 Scopus citations

Abstract

Individual isomers of β-branched α-amino acids have been stereoselective and asymmetrically synthesized in high yield by a new method which uses 4-phenyloxazolidin-2-one as a novel chiral resolution reagent acting simultaneously as the auxiliary.

Original language	English
Pages (from-to)	3057-3059
Number of pages	3
Journal	Journal of the Chemical Society, Perkin Transactions 1
Issue number	21
DOIs	https://doi.org/10.1039/p19940003057
State	Published - 1994

Access to Document

10.1039/p19940003057

Cite this

@article{7327b80e9b374e37a04dd93460ce66af,

title = "Exploration for large-scale stereoselective synthesis of unusual amino acids by using 4-phenyloxazolidin-2-one as a new chiral resolution reagent",

abstract = "Individual isomers of β-branched α-amino acids have been stereoselective and asymmetrically synthesized in high yield by a new method which uses 4-phenyloxazolidin-2-one as a novel chiral resolution reagent acting simultaneously as the auxiliary.",

author = "Guigen Li and Dinesh Patel and Hruby, {Victor J.}",

year = "1994",

doi = "10.1039/p19940003057",

language = "English",

pages = "3057--3059",

journal = "Journal of the Chemical Society - Perkin Transactions 1",

issn = "0300-922X",

number = "21",

}

TY - JOUR

T1 - Exploration for large-scale stereoselective synthesis of unusual amino acids by using 4-phenyloxazolidin-2-one as a new chiral resolution reagent

AU - Li, Guigen

AU - Patel, Dinesh

AU - Hruby, Victor J.

PY - 1994

Y1 - 1994

N2 - Individual isomers of β-branched α-amino acids have been stereoselective and asymmetrically synthesized in high yield by a new method which uses 4-phenyloxazolidin-2-one as a novel chiral resolution reagent acting simultaneously as the auxiliary.

AB - Individual isomers of β-branched α-amino acids have been stereoselective and asymmetrically synthesized in high yield by a new method which uses 4-phenyloxazolidin-2-one as a novel chiral resolution reagent acting simultaneously as the auxiliary.

UR - http://www.scopus.com/inward/record.url?scp=37049077914&partnerID=8YFLogxK

U2 - 10.1039/p19940003057

DO - 10.1039/p19940003057

M3 - Article

AN - SCOPUS:37049077914

SP - 3057

EP - 3059

JO - Journal of the Chemical Society - Perkin Transactions 1

JF - Journal of the Chemical Society - Perkin Transactions 1

SN - 0300-922X

IS - 21

ER -

Exploration for large-scale stereoselective synthesis of unusual amino acids by using 4-phenyloxazolidin-2-one as a new chiral resolution reagent

Abstract

Access to Document

Other files and links

Fingerprint

Cite this