Asymmetric synthesis of unusual amino acids: Synthesis of optically pure isomers of β-methylphenylalanine

Ramalinga Dharanipragada; Ernesto Nicolas; Geza Toth; Victor J. Hruby

doi:10.1016/S0040-4039(01)93366-0

Asymmetric synthesis of unusual amino acids: Synthesis of optically pure isomers of β-methylphenylalanine

Ramalinga Dharanipragada, Ernesto Nicolas, Geza Toth, Victor J. Hruby

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

62 Scopus citations

Abstract

All the four individual isomers of β-methylphenylalanine have been synthesized in very high optical purities by utilizing in part the chiral imide enolate bromination methodology of Evans and co-workers.

Original language	English (US)
Pages (from-to)	6841-6844
Number of pages	4
Journal	Tetrahedron Letters
Volume	30
Issue number	49
DOIs	https://doi.org/10.1016/S0040-4039(01)93366-0
State	Published - 1989
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(01)93366-0

Cite this

@article{9b90312cf9fb4339a54a3900222b7598,

title = "Asymmetric synthesis of unusual amino acids: Synthesis of optically pure isomers of β-methylphenylalanine",

abstract = "All the four individual isomers of β-methylphenylalanine have been synthesized in very high optical purities by utilizing in part the chiral imide enolate bromination methodology of Evans and co-workers.",

author = "Ramalinga Dharanipragada and Ernesto Nicolas and Geza Toth and Hruby, {Victor J.}",

year = "1989",

doi = "10.1016/S0040-4039(01)93366-0",

language = "English (US)",

volume = "30",

pages = "6841--6844",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "49",

}

TY - JOUR

T1 - Asymmetric synthesis of unusual amino acids

T2 - Synthesis of optically pure isomers of β-methylphenylalanine

AU - Dharanipragada, Ramalinga

AU - Nicolas, Ernesto

AU - Toth, Geza

AU - Hruby, Victor J.

PY - 1989

Y1 - 1989

N2 - All the four individual isomers of β-methylphenylalanine have been synthesized in very high optical purities by utilizing in part the chiral imide enolate bromination methodology of Evans and co-workers.

AB - All the four individual isomers of β-methylphenylalanine have been synthesized in very high optical purities by utilizing in part the chiral imide enolate bromination methodology of Evans and co-workers.

UR - http://www.scopus.com/inward/record.url?scp=0024791055&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0024791055&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(01)93366-0

DO - 10.1016/S0040-4039(01)93366-0

M3 - Article

AN - SCOPUS:0024791055

SN - 0040-4039

VL - 30

SP - 6841

EP - 6844

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 49

ER -

Asymmetric synthesis of unusual amino acids: Synthesis of optically pure isomers of β-methylphenylalanine

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this