N-Alkylation of diethyl acetamidomalonate: synthesis of constrained amino acid derivatives by ring-closing metathesis

Kotha, Sambasivarao ; Singh, Kuldeep (2004) N-Alkylation of diethyl acetamidomalonate: synthesis of constrained amino acid derivatives by ring-closing metathesis Tetrahedron Letters, 45 (52). pp. 9607-9610. ISSN 0040-4039

Full text not available from this repository.

Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2004.11.013

Abstract

An efficient method for N-alkylation of diethyl acetamidomalonate (DEAM) is reported. C-Alkenylation was achieved by treating the N-alkenylated DEAM with various electrophiles in the presence of Cs2CO3. RCM reactions of C- and N-alkenylated products gave cyclic amino acid derivatives in good yields.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Diethyl Acetamidomalonate; Regioselective N-alkylation; Metathesis; Constrained Amino Acid Derivatives; Heterocycles
ID Code:65166
Deposited On:15 Oct 2011 11:42
Last Modified:15 Oct 2011 11:42

Repository Staff Only: item control page