Indium triflate catalysed Ene and Friedel Crafts additions to α-imino esters: A one-pot synthesis of α-amino acid derivatives

M. Krakowski; C.G. Frost; J.P. Hartley; K.K. Chauhan

doi:10.2174/157017806775789921

Indium triflate catalysed Ene and Friedel Crafts additions to α-imino esters: A one-pot synthesis of α-amino acid derivatives

M. Krakowski
, C.G. Frost
, J.P. Hartley
, K.K. Chauhan

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

4 Citations (SciVal)

Abstract

The indium catalysed additions of electron-rich alkenes and heteroaromatics to an activated α-imino ester is described. The moisture-sensitive substrate is prepared in situ facilitating a convenient synthesis of unnatural α-amino acid derivatives in one-pot from commercially available reagents.

Original language	English
Pages (from-to)	228-230
Number of pages	3
Journal	Letters in Organic Chemistry
Volume	3
Issue number	3
DOIs	https://doi.org/10.2174/157017806775789921
Publication status	Published - 1 Mar 2006

Access to Document

10.2174/157017806775789921

Cite this

@article{571a59fc71554bd783bfc2e6511d06e8,

title = "Indium triflate catalysed Ene and Friedel Crafts additions to α-imino esters: A one-pot synthesis of α-amino acid derivatives",

abstract = "The indium catalysed additions of electron-rich alkenes and heteroaromatics to an activated α-imino ester is described. The moisture-sensitive substrate is prepared in situ facilitating a convenient synthesis of unnatural α-amino acid derivatives in one-pot from commercially available reagents. ",

author = "M. Krakowski and C.G. Frost and J.P. Hartley and K.K. Chauhan",

year = "2006",

month = mar,

day = "1",

doi = "10.2174/157017806775789921",

language = "English",

volume = "3",

pages = "228--230",

journal = "Letters in Organic Chemistry",

issn = "1570-1786",

publisher = "Bentham Science Publishers",

number = "3",

}

TY - JOUR

T1 - Indium triflate catalysed Ene and Friedel Crafts additions to α-imino esters

T2 - A one-pot synthesis of α-amino acid derivatives

AU - Krakowski, M.

AU - Frost, C.G.

AU - Hartley, J.P.

AU - Chauhan, K.K.

PY - 2006/3/1

Y1 - 2006/3/1

N2 - The indium catalysed additions of electron-rich alkenes and heteroaromatics to an activated α-imino ester is described. The moisture-sensitive substrate is prepared in situ facilitating a convenient synthesis of unnatural α-amino acid derivatives in one-pot from commercially available reagents.

AB - The indium catalysed additions of electron-rich alkenes and heteroaromatics to an activated α-imino ester is described. The moisture-sensitive substrate is prepared in situ facilitating a convenient synthesis of unnatural α-amino acid derivatives in one-pot from commercially available reagents.

UR - https://www.scopus.com/pages/publications/33746136821

UR - http://dx.doi.org/10.2174/157017806775789921

U2 - 10.2174/157017806775789921

DO - 10.2174/157017806775789921

M3 - Article

AN - SCOPUS:33746136821

SN - 1570-1786

VL - 3

SP - 228

EP - 230

JO - Letters in Organic Chemistry

JF - Letters in Organic Chemistry

IS - 3

ER -

Indium triflate catalysed Ene and Friedel Crafts additions to α-imino esters: A one-pot synthesis of α-amino acid derivatives

Abstract

Access to Document

Other files and links

Fingerprint

Cite this