Asymmetric synthesis of unusual amino acid: Synthesis of four isomers of β-methyl-3-(2'-naphthyl)alanine

Wei Yuan; Victor J. Hruby

doi:10.1016/S0040-4039(97)00770-3

Asymmetric synthesis of unusual amino acid: Synthesis of four isomers of β-methyl-3-(2'-naphthyl)alanine

Wei Yuan, Victor J. Hruby

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

24 Scopus citations

Abstract

The synthesis of all four individual isomers of 3-methyl-3-(2'-naphthyl)analine was accomplished using asymmetric conjugate 1,4-addition followed by direct or indirect azidation using an Evans-type chiral auxiliary (4-phenyl-2-oxazolidinone).

Original language	English (US)
Pages (from-to)	3853-3856
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	22
DOIs	https://doi.org/10.1016/S0040-4039(97)00770-3
State	Published - Jun 2 1997
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(97)00770-3

Cite this

@article{327fd3513db042e68d0c61545a70a2ec,

title = "Asymmetric synthesis of unusual amino acid: Synthesis of four isomers of β-methyl-3-(2'-naphthyl)alanine",

abstract = "The synthesis of all four individual isomers of 3-methyl-3-(2'-naphthyl)analine was accomplished using asymmetric conjugate 1,4-addition followed by direct or indirect azidation using an Evans-type chiral auxiliary (4-phenyl-2-oxazolidinone).",

author = "Wei Yuan and Hruby, {Victor J.}",

note = "Funding Information: Supported in part by grants from the US Public Heaith Services DK 17420and NIDA",

year = "1997",

month = jun,

day = "2",

doi = "10.1016/S0040-4039(97)00770-3",

language = "English (US)",

volume = "38",

pages = "3853--3856",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "22",

}

TY - JOUR

T1 - Asymmetric synthesis of unusual amino acid

T2 - Synthesis of four isomers of β-methyl-3-(2'-naphthyl)alanine

AU - Yuan, Wei

AU - Hruby, Victor J.

N1 - Funding Information: Supported in part by grants from the US Public Heaith Services DK 17420and NIDA

PY - 1997/6/2

Y1 - 1997/6/2

N2 - The synthesis of all four individual isomers of 3-methyl-3-(2'-naphthyl)analine was accomplished using asymmetric conjugate 1,4-addition followed by direct or indirect azidation using an Evans-type chiral auxiliary (4-phenyl-2-oxazolidinone).

AB - The synthesis of all four individual isomers of 3-methyl-3-(2'-naphthyl)analine was accomplished using asymmetric conjugate 1,4-addition followed by direct or indirect azidation using an Evans-type chiral auxiliary (4-phenyl-2-oxazolidinone).

UR - http://www.scopus.com/inward/record.url?scp=0030915528&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0030915528&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(97)00770-3

DO - 10.1016/S0040-4039(97)00770-3

M3 - Article

AN - SCOPUS:0030915528

SN - 0040-4039

VL - 38

SP - 3853

EP - 3856

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 22

ER -

Asymmetric synthesis of unusual amino acid: Synthesis of four isomers of β-methyl-3-(2'-naphthyl)alanine

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this