scispace - formally typeset
Journal ArticleDOI

A Simple One-Step Synthesis of Substituted Methyl 2-Benzoylamino-3-arylaminopropenoates, Intermediates in the Preparation of Substituted Arylaminoalanines

Branko Stanovnik, +3 more
- 01 Jan 1989 - 
- Vol. 322, Iss: 11, pp 783-787
TLDR
In this paper, a simple one-step synthesis of substituted methyl 2-benzolamino-3-anilinopropenoates 8a-r from substituted anilines 7a r and methyl 2.benzoylamino3-dimethylamin-opropoenates 6 is described.
Abstract
A simple one-step synthesis of substituted methyl 2-benzolamino-3-anilinopropenoates 8a-r from substituted anilines 7a-r and methyl 2-benzoylamino-3-dimethylaminopropenoates 6 is described. Eine einfache, einstufige Synthese substituierter 2-Benzoylamino-3-arylaminopropensauremethylester, Zwischenprodukte fur die Herstellung substituierter Arylaminoaniline. Eine einfache, einstufige Synthese der substituierten 2-Benzoylamino-3-arylaminopropensauremethylester 8a-r aus den substituierten Anilin-Derivaten 7a-r und 2-Benzoylamino-3-dimethylaminopropensauremethylester 6 wird beschrieben.

read more

Citations
More filters
Journal ArticleDOI

Parallel solution-phase synthesis of (Z)-3-(arylamino)-2,3-dehydroalanine derivatives and solid-phase synthesis of fused pyrimidones.

TL;DR: N-Protected (Z)-3-(arylamino)-2,3-dehydroalanine esters 5 and 10 were prepared in one step from methyl (Z)2-acylamino-3-(dimethylamino)prop-2-enoates 3 and 9 and anilines 4 employing a parallel solution-phase synthetic approach.
Journal ArticleDOI

Methyl 2‐benzoylamino‐3‐dimethylaminopropenoate in the synthesis of heterocyclic systems. An attempt to prepare benzoylamino substituted azolo‐ and azinopyrimidines with a bridgehead nitrogen atom

TL;DR: Methyl 2-benzoylamino-3-dimethylaminopropenoate (2) was introduced as a new reagent for the preparartion of fused pyrimidinones 4 from heterocyclic α-amino compounds in acetic acid as mentioned in this paper.
References
More filters
Journal ArticleDOI

Synthesis of gamma-L-glutaminyl-[3,5-3H]4-hydroxybenzene and the study of reactions catalyzed by the tyrosinase of Agaricus bisporus.

TL;DR: Gamma-L-glutaminyl-3,4-dihydroxybenzene was synthesized in order to study the kinetics of its hydroxylation by tyrosinase purified from Agaricus bisporus and to explore its role in the induction of the dormant state in the spores of this species.
Journal ArticleDOI

Transformations of N‐heteroarylformamidines into derivatives of β‐heteroarylamino‐α,β‐dehydro‐α‐amino acids, β‐heteroarylamino‐α‐amino acids, and dipeptides

TL;DR: In this article, a general method for the preparation of β-heteroarylamino-α, β-dehydro-α-amino acids and dipeptides is described.
Journal Article

Intracellular Activation of γ-l-Glutaminyl-4-hydroxybenzene by Tyrosinase, a Mechanism for Selective Cytotoxicity against Melanocarcinoma

TL;DR: In tests of this hypothesis, the injection of γ-l-glutaminyl-4-hydroxybenzene with probenecid significantly inhibited the growth of human melanoma in athymic mice without apparent toxicity to the cells of the host that lack the enzyme.
Journal ArticleDOI

The synthesis of β‐heteroarylamino‐α,β‐dehydro‐α‐amino acid and β‐heteroarylamino‐α‐amino acid derivatives

TL;DR: The β-heteroarylaminomethyleneoxazolones as mentioned in this paper were obtained from heterogeneous formamidines and obtained by catalytic hydrogenation the compounds were converted into βhetero-arylamino substituted amides.
Related Papers (5)